Periodontics Revisited Shalu Bathla
INDEX
A
Aberrant frenum 404
Abfraction 220
Abnormal tooth mobility 142
Abscesses of periodontium 62
Acquired immunodeficiency syndrome 144
Acrylic splints 323
Activated osteoclast 30, 180
Acute
gingival conditions 146
granulomatous necrotizing lesions of respiratory tract 142
inflammatory enlargement 138
necrotizing vasculitis 142
periodontal abscess 174
vitamin C deficiency 141
Adaptive remodeling of periodontium 202
Adrenal insufficiency 103
Advanced
implant surgery 475
lesion 131
Advantages of splinting 321
Aggressive periodontitis 191, 193, 235
Allograft 379
Alloplastic graft 379
Alveolar
bone 11, 27, 178
crest 165
fibers 17
nerve lateralization 479
ridge 407
Amalgam
and stainless steel wire splint 324
tattoo 133
Ameloblastoma 163
Androgens 207
Anesthesia 328
Antibody deficiency disorders 106
Anticalculus agents 285
Antimicrobial
mechanisms of junctional epithelium 123
system of neutrophils 84
Antioxidants 108
Apical displaced flap 354
Apically
displaced flap procedure 358
positioned flap 359
Application in periodontics 505
Application of
gene therapy 502
orthodontics 438
periodontics 417, 431, 440
photodynamic therapy 497
restorative dentistry 432
Arachidonic acid metabolism 294
Arc-shaped bone loss around mandibular first molar 192
Ascorbic acid deficiency 107
Attachment apparatus of tooth 465
Atherosclerosis 112, 113
Autogenous bone
graft 378
harvesting 476
Axillary lymph nodes 143
B
Bacteroides forsythus 61
BANA Chairside kit 242
Barrier membranes 475
Basal
bone 27
lamina 9
Basic
component of laser 490
personal protective barrier 519
steps of smoking cessation program 119
structure of laser device 490
Bass method 272
Benign tumors of gingiva 142
Beveled flap 362
Bilateral mandibular lingual exostosis 182
Bi-level orthodontic brush 271
Biofilm 65
Blade angulation 316
Bleeding indices 47
Blood supply 11, 20
Bone
architecture 367
augmentation 477
defects 177, 184
expansion 476
graft materials 378, 476
grafting technique 380
loss 178, 181
modeling and remodeling 31
morphogenetic protein 376
quality 467
resorption and formation 243
rongeur 368
Boneless window 29
Bony topography 369
Bruxism 447
C
Calculus
formation 74
indices 50
surface index 50
Candida albicans 143
Cardiovascular system 112
Cause of
halitosis 246
Wegener's granulomatosis 142
Cells 11
for tissue engineering 500
Cellular
components 29
elements 18
Cementoenamel junction 25, 35
Cementum 23
Central
giant cell granulomas 142
nervous system 449
Center of interdental papilla 13
Changes in
gingival
color 132
consistency 134
contour 133
position of gingiva 134
surface texture of gingiva 134
Charters method 272, 273
Chemical antiplaque agents 282
Chemically modified tetracyclines 293
Chemosurgery 351
Chemotherapy 497
Chisel 301
Chlorhexidine 282, 289
Chronic
gingival enlargement around orthodontic appliance 138
gingivitis 62
inflammatory
enlargement 138
gingival enlargement 138
obstructive pulmonary disease 114
periodontal abscess 174
periodontitis 62, 186188, 235
Cicatrical pemphigoid 156
Cinguloradicular/ palatogingival groove 259
Classification of
local drug delivery 288
marginal tissue recession 400
papillary height 407, 408
parafunctional habits 446
periodontal
diseases 39, 41, 337
flaps 355
perio-endo lesions 426
pocket according to involved tooth surface 165
ridge defects 407, 408
smokers 116
soft tissue procedures used for root coverage 400
Classifying periodontal diseases 196
Coagulation disorders 105
Col 3
Combined diseases 427
Commonly used chemotherapeutic 281
Community periodontal index of treatment needs 52
Complement system 84
Complete denture and removable
denture 419
Complex genetic diseases 97
Composite
and wire splint 324
splints 323
Composition of
calculus 74
GCF 126
saliva 124
Compression suture to control bleeding 340
Conditioned gingival enlargement 140, 141
Connective tissue 2, 356
interface 9
Constituents of tobacco smoke 116
Continuous
disease model 188
horizontal mattress sutures 335
incision 350
sutures 335
Conventional needle holder 308
Coronally displaced flap 364, 403
Corticosteroid hormones 103
Crater 182
Criss cross horizontal mattress suture 335
Crossbite 221
Crown 418, 419
and root surface 35
morphology 434
Curette 302
blade 298
Curved jeweler microforcep 413
Cut-back incision 355
Cyclosporine induced gingival enlargement 139
D
Decontamination of dental instruments 522
Deepbite 221
Defense mechanisms of gingiva 123
Definition of
periodontal flap 355
plaque 65
Dental
calculus 72
caries 218
floss in loop 276
implant failure 472
laser safety 495
mirrors 298
plaque 62, 65
Dentascan 467
Dentin hypersensitivity 251
Dentinal hypersensitivity 254
Denture
brush 422
plastics 420
Design of
cohort study 44
prosthesis 420
Desquamative gingivitis 155
Development of
periodontal classification system 39
principal periodontal ligament fibers 17
Developmental gingival enlargement 144
Diabetes mellitus 101, 102, 113, 114
Different types of pocket 165
Direct loop suture 331
Discontinuous incision 350
Discoveries in periodontics 524
Distal molar surgery 362
Distalization of mental neurovascular bundle 479
Distraction osteogenesis 477
Distribution of cementum on tooth surface 24
Donor-cell derived oral squamous cell carcinoma 159
Double papilla
flap procedures 402
pedicle flap 364
Drug
induced gingival enlargement 138
therapy 109
E
Edlan-Mejchar
operation 407
procedure 405
Electrosurgery 350
Endocrine system 113
Endodontic infection on periodontium 426
Enzymes released by dead cells 243
Epidemiology of gingival and periodontal diseases 43
Epinephrine 449
Epithelial
graft 397
odontogenic ghost cell tumor 162
Epithelium 9
and gingival connective tissue 372
Erosive lichen planus 156
Erythema multiforme 158
Estrogen 206
Excisional new attachment procedure 344
Exfoliation of teeth 142
Exostoses 369
Extension of gingival inflammation 178
Extent and severity index 53
Extracoronal type of splints 322
Extraoral palm
down fulcrum 316
up fulcrum 316
Extrasulcular methods 125
F
Facemask 519
Factors
determining bone morphology 177
influencing tooth position 203
Female sex hormones and periodontium 206
Fibroma 142
of gingiva 142
Fibrosseous integration 463
Figure of eight suture 332
Fixed partial prosthesis 77, 422
Flap
design 328
height-to base ratio 329
management for ridge augmentation 476
reflection 328, 329
Fones method 273
Formation of preosteoclast 179
Forms of subgingival calculus 73
Fremitus test 221
Frenectomy 404, 405
Fulcrum 314
Full thickness flap 175
Functions of
GCF 126
macrophage 82
neutrophil 82
Furcation 234
defect 188, 277
G
Galilean compound loupe 412
Gene
therapy 502
in periodontics 510
transfer techniques 502
Genetic basis of periodontal diseases 96
Gingiva 3, 4, 104, 221, 397
Gingival
abscess 174
and periodontal inflammation 78
bleeding 131
index 48
blood supply 11
clefts 133
connective tissue 9, 141
crevicular fluid 125
curettage 343
cyst 162
diseases 41, 259
edema 140
enlargement 137, 142
epithelium 6
extension using periosteal fenestration 405
fibers 9, 10
health 89
hyperplasia 77, 441
indices 46
inflammation 129, 141, 187
margin 35
recession 400
sulcus 125
Gingivectomy 347, 351, 352
knives 307
Gingivitis 131
seen during menstrual cycle 208
Gingivoplasty 348
Glickman's concept 200, 201
Gloves 520
Gracey curettes 303, 318
Gradualizing marginal bone 369
Grafting procedure 398
Granulation tissue 175
Granulomatous
diseases 142
gingivitis 163
papillary enlargement 142
GTR membrane 375
Guided
bone regeneration 475
tissue regeneration 372
H
Halitosis 245, 249
Hard tissues 163
Head of powered toothbrush 270
Healing of free epithelial graft 399
Hemorrhage 141, 339
Hemostasis 329
Herpetic gingivostomatitis 151
Histopathology of periodontal abscess 173
Horizontal bone loss 188, 234
Host
modulatory
agents 292
therapies 293
tissue
destruction 91
invasion 90
Human papillomavirus 142
Hyperplastic gingiva 140
Hypersensitivity measurement 253
I
Idiopathic
gingival fibromatosis 139, 140
hyperplastic gingival enlargement 135
Immediate implant placement 472
Immunodeficiency disorders 105
Immunoglobulin molecule 86
Implacare implant
instrument 485
maintenance instrument 306
Implant
peri-implant mucosa 465
surgery 469
system 471
Impression materials 419, 421
Incisions 354
for distal molar surgery 363
used in periodontal surgery 353
Indications for
periodontal surgery 327
use of antibiotics in periodontal therapy 286
Indications of microbiologic assays 239
Indications of
ostectomy 367
osteoplasty 367
Inferior alveolar lateralization 479
Interdental
brush 276
cleaning aids 275
craters 369
septa 233
septum 28
Internal bevel incision 357
Interpositional onlay graft 409
Interproximal
bone loss 433
embrasure spaces 275
Intrabony defect 181
Intracoronal type of splints 323
Intraoral periapical radiograph 232
Intrusion 438
J
Jaws 236
Junctional
epithelial cells 123
epithelium 6, 7, 123
Junctions of cementum 25
K
Kaposi's sarcoma 144
Kirkland knife 307, 349
Kissing roots 28
Koch's postulates 59, 60
L
Lamina propria 9
Laser
delivery systems 490
emission modes 490
energy and tissue temperature 491
gingivectomy 349
tissue interactions 492
uses in periodontics 492
Laterally positioned pedicle flap 364, 401
Lekholm and Zarb classification 1985 467
Leukemia 104, 142
Leukemic
cells 142
gingival enlargement 142
Leukocyte disorders 105
Leukoplakia 143
Lichen planus 155
Lipopolysaccharide 293
Lipping of alveolar bone 202
Local drug delivery system 288
Localized aggressive periodontitis 62, 192
Lower left central incisor 172
Lupus erythematosus 158
M
Macrodesign of implants 461
Macrophages 81
Magnification systems 411
Magnifying loupes 411
Maintenance of periodontal ligament
space 20
Malignant
lesions of gingiva 159
lymphoma 143
melanoma 143, 159
tumors of gingiva 143
Mandibular
anterior teeth 73
teeth 277
Manual toothbrushes 269
Marginal
gingivitis 129
line calculus index 51
tissue recession 223, 400
Marquis color coded probe 299
Mast cells 81
Matrix metalloproteinase 92, 293, 449
Mattress suture 335
Measurement of GCF 126
Melanin pigmentation 12
Menopause 210
Menstrual cycle 207
Metal intoxication 108
Metastatic tumors in jaws 158
Methods of
collection of GCF 125
genetic analysis 97
Microneedle holder 413
Microscissor 413
Mini bladed curette 303
Minimally invasive surgery 507, 508, 510
Mixed tumors 143
Modified
gingival index 47
pen grasp 314
Stillman's method 272, 273
Widman flap 354, 357
procedure 356
Molecules for tissue engineering 501
Mouth breathing 448
N
Nanotechnology in periodontics 510
Nasal and oral defects 142
Necrotizing
periodontal disease 62
ulcerative gingivitis 146, 148, 451
Nerve supply 12, 20
Night guards 322
Non-Hodgkin's lymphomas 143
Non-mineralized bone matrix 180
Norepinephrine 449
Normal
bone contour 182
gingiva 12
Novel design toothbrush 271
O
Occlusal
cupping of molar 220
surface 421
Ochsenbein chisel 308, 368
Open gingival embrasures 432
Operculectomy 153
Oral
contraceptives 210
debris index 50
diseases 125
epithelium 6
health 124
mucosal ulceration 142
Orban's
interdental knife 307
knife 349
Origin of junctional epithelium 7
Orofacial granulomatosis 163
Orthodontic
bi-level toothbrush 441
brush 271
tooth movement 440
toothbrushes 270
treatment of osseous defects 438
Osmotic method 252
Osseointegration 462
Osseous
crater 182
defects 234
Osteoblast 31
Osteoclast 31
Osteosarcoma 163
Osteotomy 478
Overhanging restorations 236
P
PD Miller's classification of marginal tissue recession 401
Palatal flap 361
Palatogingival groove 76
Palm and thumb grasp 314
Palpating
submandibular and sublingual lymph nodes 217
TMJ 217
Panoramic oral radiograph 232
Papilla preservation flap 360
incisions 361
Papillary
bleeding index 48
frenum 223
gingivitis 130
marginal attached index 46
Papilloma 142
Parathyroid glands 103
Partial
prosthesis 422
thickness flap 356
Parts of
periodontal instrument 296
surgical needle 329
toothbrush 269
Pathogenesis of periodontal disease 94
Patient hygiene performance index 49
Pemphigus 156, 157
vulgaris 156
Periapical abscess 174
Pericoronitis 143, 152, 153
Peri-implant mucositis 481
Peri-implantitis 481, 482
Perio test 463, 465
Periodontal
abscess 171, 228
aspects of psychiatric patients 451, 452
diseases 35, 41, 90, 94, 112114, 117, 177, 232, 235, 450
and host response 89
dressings 336338
effects of smoking cessation 119
endodontic lesions 429
endoscope 305
epidemiology 45
file 301
flap 353, 355
health 62, 440
index 51
infection on pregnancy outcome 114
instruments 296
lesions on pulp 425
ligament 11, 16
fibers 17
space 233
manifestations 207, 208, 210
microbiology 59
microsurgery 411
pack placement 338
pocket 167
probes 299
surgery 327, 328, 380
for placement of restoration 431
therapy 119, 265
tissue engineering 499, 501
treatment procedures on dental pulp 426
vaccine 506, 510
Periodontics 281, 432, 438, 446, 492, 502
endodontics 424
oral surgery 443
orthodontics 436
prosthodontics 417
restorative dentistry 431
Periodontitis 98, 143, 192, 259
in HIV 198
Periodontium 206, 233
Perio-endo lesions 425
Periosteal elevator 308
Peripheral
ameloblastoma 162
fibroma 160, 161
cell
granuloma 142
tumor 161
odontogenic
keratocysts 162
lesions 162
ossifying fibroma 160, 161
Peroxide 284
Phenytoin 109, 139, 452
Photodynamic therapy 496, 509
Piezoelectric ultrasonic unit 304
Pituitary gland 103
Plaque
biofilm 66
component of periodontal disease index 48
formation 68
hypothesis 69
indices 48
Plasma cell
gingivitis 141
gingivostomatitis 141
granuloma 141
Plastic
probe 483
surgery 396
Platelet rich plasma 377
Plunger cusp 219
Polymorphonuclear leukocytes 124
Porphyromonas gingivalis 61
Povidone iodine 284
Powered toothbrushes 270
Pregnancy tumor 141, 209
Preprosthetic periodontal
care 417
surgery 418
Pre-restorative periodontal care 431
Prevotella intermedia 140
Pricking gingiva with fingernail 79
Primary
endodontic lesion 426, 427
herpetic gingivostomatitis 150
Principal periodontal ligament fiber groups 17
Principles of
flap design 355
scaling and root planing 317
suturing 330
tissue engineering 499
Prismatic loupe 412
Progesterone 207
Proliferative verrucous leukoplakia 159
Prostaglandins 92
Prosthetic dentistry 417
Puberty 207
gingivitis 207
Pus discharge 224
Pyogenic granuloma 141, 143, 160
Q
Quarternary ammonium compounds 283
R
Random burst disease model 188
Rationale of using antimicrobial agents 286
Reactive lesions of gingiva 160
Red blood cell disorders 105
Re-emergence of focal infection theory 111
Reflected papilla preservation flap 361
Regenerative osseous surgery 371
Relation of face to lower shank 303
Removing of gloves 521
Reproductive system 113
Resecting gingival margin 403
Resective osseous 369
surgery 366, 367
Resonance frequency analysis 466
Respiratory system 114
Restoration of root-resected teeth 432
Restorative dentistry 431, 433
Retraction of tongue 312
Retrograde periodontitis 427
Reusable floss holder 277
Ridge augmentation 419
Rochette splint 322
Role of
calculus in periodontal disease 75
saliva 124
Root biomodification 375
S
Saliva 124
Salivary gland type tumors 143
Sarcomas 160
Scaffolds for tissue engineering 499
Scaling and root planing 329
Scalpel 413
handle-bard-parker handles 307
Schluger
file 368
surgical file 308
Scissors and nippers 309
Scoring of gingival enlargement 138
Scrub method 274
Scurvy 141
Semilunar coronally
displaced flap procedure 404
repositioned flap 403
Sequence of
periodontal therapy 267, 513
toothbrushing 274
Serial antimicrobial therapy 286
Severe pregnancy gingivitis in lower anterior teeth 208
Severity of periodontal disease 117
Sex hormones 103, 206, 211
on periodontium 207
Shallow incision 350
Shank design 297
Sharpey's fibers 18
Sickle scaler 300
Simple mendelian diseases 97
Simplified-oral hygiene index 50
Sinus
bone grafting 477
elevation 477
lift procedure 478
membrane is scrapped off bone 478
Sling suture 333
Smoking
and periodontal diseases 118
and periodontium 116
cessation 119
Socransky's criterion 60
Soft
and hard tissue lesions 155
tissue 462
Specific
acquired immunity 86
osseous reshaping situations 369
Splinting 320, 321, 432
Squamous
cell carcinoma 143, 159
epithelium 6
Stages of gingivitis 130
Standard pen grasp 314
Sterilization methods 523
Stillman's
method 273
clefts 133
Straight and angled shank toothbrushes 269
Stress and psychosomatic disorders 108
Stroke directions 317
Subepithelial connective tissue graft 400
Subgingival
calculus 73, 75, 236
environment 112
plaque 63
Sulcular epithelium 6
Sulcus bleeding index 47
Superfloss 277, 422
Supportive periodontal therapy 513
Suprabony pocket 165
Supraerupted tooth 369
Supragingival calculus 73
Supraperiosteal vessels 11
Surgical
aspects of implants 469
blades 307
chisel 308
and hoes 307
curettes and sickles 307
gingivectomy 349
instruments 306, 349, 357, 358
operating microscope 412
Suture needles 330
Sutured knots 334
Swelling 340
Systemic
diseases 142
disorders 180
lupus erythematosus 157
spread of periodontal infection 112
T
Tactile method 253
Tannerella forsythia 61
Teeth 218
Tetracyclines 293
Theories of dentin sensitivity 252
Therapy in periodontics 503
Thermal test 253
Thickening of lamina dura 203
Thickness of cementum 25
Thin gingival phenotype 5
Thrombocytopenia 105
Thumb sucking 447
Thyroid gland 103
Tissue
engineering 498, 509
healing 92
nipper 308, 349
Titanium plasma spray 462
Tobacco stains 71, 78
Tongue thrusting 448, 449
habit 222
Tooth
brushing
abrasion 78
methods 271
eruption 35
migration 202
supporting alveolar process 28
surface and implant 75
Traditional oral hygiene methods 268
Transendothelial migration 83
Transgingival probing/bone sounding 227
Treatment of
peri-implant pathology 483
periodontal diseases in HIV 198
Triclosan 284
Turesky modification of Quigley-Hein plaque index 49
Two stage implant
surgery 469, 470
system 469
Types of
explorers 298
finger rests 315
gingivectomy procedure 349
needles 330
scaffolds 499
suture materials 330
suturing 331
U
Ulcerative gingivitis and stress 451
Ultrasonic
and sonic instruments 304
curettage 345
Underlying
dental tissues 144
osseous lesions 144
Undisplaced flap 354, 358
flap procedure 358
Unituft brush 276
Universal curette blade 302
V
VAS-visual analog scale 254
Verbal rating scale 253
Verrucous leukoplakia 159
Vertical
bone loss 181, 188, 234
grooving 369
incision 174, 354
mattress suture 334
method 273
osseous defects 181
Vestibuloplasty 407
Viral methods 502
Vitamin C deficiency 107, 141
V-M calculus assessment 51
W
Waerhaug's concept 201
Walking stroke 225
Wearing of gloves 521
Wegener's granulomatosis 142
Welded band splints 322
Williams probe 299
Wire
ligation 322, 323
splinting 323
X
Xenogenic graft 379
×
Chapter Notes

Save Clear


1
NORMAL PERIODONTIUM2

GingivaCHAPTER 1

Shalu Bathla
 
DEFINITION
Gingiva is the part of oral mucosa that covers the alveolar processes of the jaws and surrounds the necks of the teeth.
 
MACROSCOPIC FEATURES
Anatomically, the gingiva is classified into three distinct domains: Free/marginal gingiva, attached gingiva and interdental gingiva (Fig. 1.1).
  1. Free gingiva
  2. Interdental gingiva
  3. Attached gingiva
  1. Marginal gingiva is the terminal edge of the gingiva surrounding the teeth in a collar – like fashion. The marginal gingiva is called free as it is not attached to the underlying periosteum of alveolar bone. The gingival margin is demarcated from attached gingiva by an indentation called as free gingival groove which is positioned at a level corresponding to the level of the cementoenamel junction (CEJ). Free gingival groove is only present in about 30–40% of adults. Functionally, the marginal gingiva forms the soft tissue wall of the V - shaped gingival sulcus. Gingival sulcus is a shallow groove between the tooth and normal gingiva that extends from the free surface of the junctional epithelium coronally to the level of free gingival margin.
  2. Interdental gingiva is the part of the gingiva which is present in the interdental space beneath the area of tooth contact. In the presence of diastema the interdental papilla is absent (Fig. 1.2).
    Col is a valley like depression which connects the facial and lingual papillae and conforms to the shape of the interproximal contact areas (Fig. 1.3). Col epithelium is identical to junctional epithelium having the same origin (from dental epithelium), non-keratinized and gradually replaced by continuing cell division.
  3. Attached gingiva is firm, resilient and tightly bound to the underlying periosteum of alveolar bone and cementum by connective tissue fibers. The attached gingiva is thus, firmly entrenched between two movable structures – the marginal gingiva coronally and the alveolar mucosa apically.
4
zoom view
Fig. 1.1: Macroscopic features of gingiva
zoom view
Fig. 1.2: Absence of interdental papilla in the diastema
zoom view
Fig. 1.3: Showing col and peaks
Width of attached gingiva: It is the distance between mucogingival junction and the projection on the external surface of the bottom of gingival sulcus/periodontal pocket. The dimensions of the attached gingiva vary from the anterior to the posterior teeth. Width of attached gingiva on facial aspect of – maxillary incisor region is 3.5 to 4.5 mm, mandibular incisor region is 3.3 to 3.9 mm, maxillary first premolar is 1.9 mm and mandibular first premolar is 1.8 mm approx. Width of attached gingiva increases with age and in supraerupted teeth. This increase in dimension occurs as a result of an increase in the height of the alveolar process which in turn is the result of passive eruption.
Significance of attached gingiva:
  1. It gives support to the marginal gingiva.
  2. It provides attachment or a solid base for the movable alveolar mucosa for the action of lips, cheeks and tongue.
  3. It can withstand frictional and functional stresses of mastication and toothbrushing. When the marginal tissue is alveolar mucosa, it does not resist the functional stresses of toothbrush trauma imposed on it. Frequently, the result is apical shifting of the marginal tissue and additional recession. Attached gingiva has more densely organized connective tissue and is more firmly bound to the underlying periosteum and bone. Consequently, it is more resistant to the functional stresses placed upon it. Alveolar mucosa is thin, delicate tissue, poorly attached to bone and cementum and is not capable of withstanding these same functional stresses.
    5
  4. Attached gingiva acts as a barrier for passage of inflammation. A tooth having alveolar mucosa at its margin seems to show clinical signs of inflammation in the presence of microbial flora more readily than does a corresponding tooth that has a sufficient band of attached gingiva. Such marginal tissue appears to be more susceptible to the products of inflammation that may result in pocket formation or apical migration of both attachment apparatus and marginal tissues.
  5. It provides resistance to tensional stresses. Attached gingiva serves as a buffer between the mobile free gingival margin and mobile alveolar mucosa. There are skeletal muscle fibers within the alveolar mucosa that exert a force in an apical direction on the attached gingiva. This force is dissipated by bound down keratinized tissue.
Width of attached gingiva can be measured:
  1. Anatomically: Stretch the lip/cheek to demarcate the mucogingival line while pocket is being probed. Measure the total width of gingiva (gingival margin to mucogingival line) and subtract the sulcus/pocket depth from it to determine width of attached gingiva.
  2. Functionally:
    • Tension test: Stretch the lip or cheek outward and forward to mark mucogingival line. Measure the total width of gingiva (gingival margin to mucogingival line) and subtract the sulcus/pocket depth from it to determine width of attached gingiva.
    • Roll test: Push the adjacent mucosa coronally with a dull instrument to mark mucogingival line. Measure the total width of gingiva (gingival margin to mucogingival line) and subtract the sulcus/pocket depth from it to determine width of attached gingiva. A more reliable method of identifying the mucogingival junction would be to take the side of a periodontal probe or similar blunt instrument and jiggle the alveolar mucosa in an apicoronal direction. Since the alveolar mucosa is mobile, it will roll up ahead of the blunt instrument.
  3. Histochemically: Iodine staining test: Paint the gingiva and oral mucosa with Schiller's or Lugol's solution (iodine and potassium iodide solution). The alveolar mucosa takes on a brown color owing to its glycogen content, while the glycogen free, attached gingiva remains unstained. Measure the total width of the unstained gingiva and subtract the sulcus/pocket depth from it to determine width of attached gingiva.
    The other dimension that may play a significant role in the maintenance of the periodontal health is the thickness of the gingiva. Gingival phenotype or biotype has been classified by Eger and Muller into thick and thin or Class I, IIA and IIB. Thick gingival phenotype seems to be more conducive to periodontal health. A thin phenotype predisposes to gingival recession and increased tendency to gingival inflammation (Fig. 1.4).
Mucogingival junction is the interface between the apically located alveolar mucosa and the coronally located attached gingiva which remains stationary throughout life. Mucogingival junction is present on the three gingival surfaces namely facial gingiva of the maxilla, facial and lingual gingiva of the mandible. The palatal gingiva of the maxilla is continuous with the tissue of the palate, which is bound down to the palatal bones. Because the palate is devoid of freely movable alveolar mucosa, there is no mucogingival junction.
zoom view
Fig. 1.4: Thin gingival phenotype
TABLE 1.1   Differences between alveolar mucosa and attached gingiva
Alveolar mucosa
Attached gingiva
1. Color
2. Surface texture
3. Epithelium
4. Connective tissue
Red
Smooth and shiny
• Thinner
• Rete pegs absent
• Nonkeratinized
• More loosely arranged
• More blood vessels
Pink
Stippled
• Thicker
• Rete pegs present
• Parakeratinized
• Not so loosely arranged
• Moderate blood vessels
6
 
MICROSCOPIC FEATURES
Histologically, gingiva is composed of gingival epithelium, epithelium-connective tissue interface and underlying connective tissue.
 
Gingival Epithelium
The gingival epithelium is comprised of oral epithelium, sulcular epithelium and junctional epithelium (Fig. 1.5 and Table 1.2).
  1. Oral epithelium/outer epithelium: It covers the crest and outer surface of marginal gingiva and surface of the attached gingiva. It is a keratinized stratified squamous epithelium.
    zoom view
    Fig. 1.5: Microscopic features of gingiva: A. oral epithelium, B. Sulcular epithelium, C. Junctional epithelium
    TABLE 1.2   Differences between oral, sulcular and junctional epithelium
    Oral
    Sulcular
    Junctional
    1. Keratinization
    Keratinized
    Nonkeratinized
    Nonkeratinized
    2. Rete pegs
    Present
    Absent
    Absent
    3. Strata granuloma and corneum
    Present
    Lacking
    Lacking
    4. Merkel cells
    Present
    Absent
    Absent
    5. Langerhans cells
    Present
    Few
    Absent
    6. Type IV collagen in basal lamina
    Present
    Absent
    Absent
    7. Tight junctions
    More
    Few
    Few
    8. Acid phosphatase activity
    Present
    Lacking
    Lacking
    9. Glycolytic enzyme activity
    High
    Lower
    Lower
    10. Intercellular space
    Narrower
    Narrower
    Wider
    Following are the layers of oral epithelium (Fig. 1.6):
    • Stratum basale: The cells are either cylindric or cuboid. The basal cells are found immediately adjacent to the connective tissue and are separated from connective tissue by a basement membrane. It is the germinative layer, having the ability to divide. When two daughter cells have been formed by cell division, an adjacent older basal cell is pushed into the spinous cell layer and starts, as a keratinocyte, to traverse the epithelium. It takes approximately 1 month for a keratinocyte to reach the outer epithelial surface, where it is shed from the stratum corneum.
    • Stratum spinosum: It is a prickle cell layer in which large polyhedral cells with short cytoplasmic processes are present. The uppermost cells of this layer contain granules called as keratinosomes or Odland bodies, which are modified lysosomes. They contain a large amount of acid phosphatase, an enzyme which is involved in the destruction of organelle membranes.
    • Stratum granulosum: Cells of this layer are flattened in a plane parallel to the gingival surface. Keratohyaline granules which are associated with keratin formation are (1 µm in diameter) round in shape and appear in the cytoplasm of the cell.
      zoom view
      Fig. 1.6: Representative cells of various layers of stratified squamous epithelium
      7
    • Stratum corneum: It consists of closely packed, flattened cells that have lost nuclei and most other organelles as they become keratinized. The cells are densely packed with tonofilaments. Clear, rounded bodies probably representing lipid droplets appear within the cytoplasm of the cell.
  2. Sulcular epithelium: It lines the gingival sulcus. It is a non-keratinized, stratified squamous epithelium which extends from the coronal end of the junctional epithelium to the crest of the gingival margin.
  3. Junctional epithelium (JE): Junctional epithelium consists of collar like band of stratified squamous nonkeratinized epithelium. The normal length of junctional epithelium is 0.25–1.35 mm.
 
Development/Origin of Junctional Epithelium
Before the tooth begins its eruptive movements, the crown of the tooth is covered by a double layer of epithelial cells. The inner layer of cells called ameloblasts which have completed their formative function, develops hemi-desmosomes and becomes firmly attached to the enamel surface. The outer layer consists of more flattened cells, the remnants of all the remaining layers of the dental organ. Together these two layers are called as reduced enamel epithelium. Connective tissue present between this reduced enamel epithelium and the overlying oral epithelium breaks down, and degenerates when the tooth eruption begins in the oral cavity. The cells of the outer layer of reduced enamel epithelium and the basal cells of the oral epithelium proliferate and migrate into the degenerative connective tissue and thus eventually fuse to establish a mass of epithelial cells over the erupting tooth. Cell death in the middle of this epithelial plug leads to the formation of an epithelium-lined canal through which the tooth erupts without hemorrhage. From this mass of epithelium, together with the remaining reduced dental epithelium, the epithelial component of dentogingival junction is established. The reduced ameloblasts, which have lost and do not regain the ability to divide, change their morphology and are transformed into squamous epithelial cells that retain their attachment to the enamel surface. The cells of the outer layer of reduced enamel epithelium which retain their ability to divide, become and function as basal cells of a forming junctional epithelium.
It was first named epithelial attachment (Epithe-lansatz) by Gottlieb, but later it was examined electron microscopically and was renamed as junctional, or attachment epithelium by Stern. This epithelium synthesizes the material that attaches it to the tooth. This material, its morphology, mode and mechanism of function, is what is now called the epithelial attachment. Thus, the cellular structure is referred to as junctional or attachment epithelium and its extracellular tooth attaching substance is referred to as the epithelial attachment.
Junctional epithelium is divided into three zones: the apical, middle and coronal zone. The middle zone is the zone with the maximum adhesiveness, and the coronal zone is the most permeable of the three zones.
Junctional epithelium has three surfaces: internal surface which faces the tooth surface, external surface which faces the gingival connective tissue and coronal surface of the junctional epithelium forms the base of the sulcus. Junctional epithelium is attached to the tooth surface by means of internal basal lamina and to gingival connective tissue by an external basal lamina. The attachment of junctional epithelium to the tooth is mediated through an ultramicroscopic mechanism defined as the epithelial attachment apparatus. It consists of hemidesosomes at the plasma membrane of the cells directly attached to the tooth (DAT cells) and a basal lamina like extracellular matrix, termed the internal basal lamina, on the tooth surface (Fig. 1.7).
Junctional epithelium is easily penetrated because of the following factors:
  1. Along the junctional epithelium, subepithelial vessels are parallel to the surface and are made up mostly of venules rather than capillaries. These venules have a greater disposition towards increased permeability than do capillaries and arterioles and they are more susceptible to hemorrhage and thrombosis.
    zoom view
    Fig. 1.7: Junctional epithelium
    8
  2. Few intercellular tight junctions
  3. Minimal cytoplasmic filaments
  4. Higher number of intercellular spaces
  5. Lower number of desmosomes.
Functions: Junctional epithelium serves many roles in regulating tissue health:
  1. Provides attachment to the tooth.
  2. Acts as barrier attached to the tooth and thus forms an epithelial barrier against the plaque bacteria. External basement membrane laterally forms an effective barrier against invading microbes.
  3. Rapid cell division and funneling of junctional epithelial cells towards the sulcus hinder bacterial colonization and repair of damaged tissue occurs rapidly.
  4. Allow GCF flow—Junctional epithelium allows the access of GCF, inflammatory cells and components of the immunological host defense to the gingival margin. Junctional epithelium allows two - way movement of variety of substances: a). From connective tissue into crevice – Gingival fluid exudates, PMNs, Ig, complement and various cells of immune system; b. From crevice to connective tissue – Foreign material such as carbon particles, trypan blue.
  5. Active antimicrobial substances are produced by junctional epithelial cells. These include defensins, lysosomal enzymes, calprotectin and cathelicidin.
  6. Epithelial cells activated by microbial substances secrete chemokines, e.g. IL-1, IL-6, IL-8 and TNF-α that attract and activate professional defense cells such as lymphocytes and PMNs.
Cells present in the gingival epithelium are namely keratinocytes and non- keratinocytes:
  1. Keratinocytes: These make up 90% of the total gingival cell population. They originate from the ectodermal germ layer. Structurally, keratinocytes are like any other cells having cell organelles like nucleus, cytosol, ribosomes, Golgi apparatus. Keratinocytes have melanosomes, which are the pigment bearing granules present in these cells only and not in the other cells of periodontium. The main function of the gingival epithelium, i.e. protection and barrier against the oral environment is achieved by the proliferation and differentiation of the keratinocytes. Keratinocytes have to move from basal to superficial layers of the epithelium as the process of differentiation occurs in a basocoronal direction culminating in the formation of a keratin barrier. The microfilaments present in the keratinocytes help in cell motility and maintenance of the polarity.
    Keratinocyte motility requires the following steps:
    • Development of lamellopodia, i.e. extensions on the leading edge of the cell towards the direction of movement.
    • Attachment of this portion of the cell to the substratum.
    • Movement of the cytosolic material towards the leading edge of the cell.
    • Detachment of the rear end.
  2. Non-keratinocytes/Clear cells: The various non-keratinocytes are langerhans cells, merkel cells and melanocytes.
Langerhans cells (LCs) are modified monocytes belonging to reticuloendothelial system which reside chiefly in suprabasal layers. They are responsible for communication with immune system by acting as antigen – presenting cells for lymphocytes. These cells containg - specific elongated granules called as Birbecks granules and have marked adenosine triphosphatase activity. Paul Langerhans used gold impregnation technique 100 years ago to visualize LCs. they are the only epidermal cells which express receptors for C3 and Fc portion of IgG. Langerhans cells can move in and out of the epithelium unlike melanocytes.
Merkel cells are located in deeper layers of epithelium. These are not dendritic cells as melanocytes and langerhans cells. These cells possess keratin tonofilaments and occasional desmosomes which link them to adjacent cells. Merkel cells are sensory in nature and respond to touch.
Melanocytes originate from neural crest cells found in the stratum basale of the gingival oral epithelium. Oral mucosal melanocytes were identified in gingiva by Laidlaw and Cahn in 1932. These cells have long dendritic processes that are found interspersed between the keratinocytes of the epithelium. They lack tonofi-laments and desmosomal connection to adjacent keratinocytes. Melanocytes are the cells which are responsible for the barrier to UV damage and synthesize melanin which is responsible for providing color to gingiva. Melanin is synthesized in organelle called premelanosomes/melanosomes in melanocytes cells. Melanosomes are transported along microtubules and actin filaments to the cell periphery. Melanocytes bind to the plasma membrane and transfer the melanosomes to adjacent keratinocytes (Fig. 1.8). The precise mechanism is unknown, but has been described as cytocrine secretion.
9
zoom view
Fig. 1.8: Mechanism of melanosome transport
Sometimes, in the connective tissue macrophages take up the melanosomes produced by melanocytes in the epithelium and are called as melanophages/melanophores. Melanocytes may be classified as active or inactive, depending on presence or absence of mature melanosomes. The ratio of melanocytes to keratinocytes producing epithelial cells is approx. 1:36 cells.
 
Epithelium—Connective Tissue Interface
Ultrastructurally, epithelial – connective tissue interface is composed of 4 elements namely basal cell plasma membrane with its specialized attachment devices (hemidesmosomes), lamina lucida an electrolucent zone of 25 to 45 nm wide and lamina densa an electrodense zone of 40 to 60 nm thickness where type IV collagen is present and last is reticular layer. From the lamina densa so called anchoring fibrils project in a fan-shaped fashion into the connective tissue (Fig. 1.9).
The various junctional complexes present in gingiva are:
  • Tight/occluding junctions are formed by the fusion of external leaflets of adjacent cell membranes at a series of points.
  • Adhesive junctions:
    Cell to cell
    • Zonula adherens
    • Desmosomes: It is the most common type of junction which consists of two adjacent attach-ment plaques one from each cell that are separated by an interval of approx. 30 nm.
    zoom view
    Fig. 1.9: Basal lamina—Junction between epithelium and connective tissue
    Cell to matrix
    • Focal adhesions
    • Hemidesmosomes
  • Communicating (gap) junctions: They have intercellular pipes/channels that apparently bridge both the adjacent membranes and intercellular space. The intercellular space in gap junction is approx. 3 nm and is the major pathway for direct intercellular communication.
 
Gingival Connective Tissue / Lamina Propria
The gingival connective tissue consists of gingival fibers, various cells and ground substance.
 
Gingival Fibers
Fibers in human gingiva are made up of collagen, reticulin and elastin. Collagen fibers make up more than 50% of the volume of human gingiva. Types I, III, IV, V, VI of collagen are present in gingiva. Type I collagen predominates. The structural formula for type I collagen is [α1 (I)]2 α2. Type III collagen is fetal collagen which is important in the early phases of wound healing and remains in an unmineralized form. Type III collagen in the gingiva is partly responsible for the maintenance of space in the healing matrix. Type IV collagen is present in the lamina densa layer of the basement membrane of the epithelium. Type VI collagen is distributed with the elastin fibers along the blood vessels. The type VI collagen fibers impart rigidity required to maintain the elastic blood vessel wall from undergoing permanent deformation. Type VII collagen acts as anchoring fibrils that help to reinforce epithelial attachment to the underlying connective tissue.
zoom view
10
The functions of these fibers are:
  1. To stabilize the attached gingiva to the alveolar process.
  2. To stabilize the attached gingiva to the tooth.
  3. Helps to maintain the epithelial seal to the tooth.
  4. To provide stability to the tooth.
  5. To brace marginal/free gingiva firmly against the tooth and adjacent attached gingiva.
  6. To provide rigidity to withstand forces of mastication without being deflected away from the tooth surface.
Gingival fibers are arranged into following groups (Fig. 1.10):
  1. Dentogingival group: These fibers extend from the cementum apical to junctional epithelium and course laterally and coronally into lamina propria of the gingiva. These provide gingival support.
  2. Alveologingival group: These fibers arise from the alveolar crest and insert coronally into lamina propria of the gingiva. Attaches attached gingiva to alveolar bone.
  3. Circular group: This group of fibers encircle the teeth in a cuff or ring like fashion. Maintain contour and position of free marginal gingiva.
  4. Transseptal fibers: These are the group of prominent horizontal fibers located interproximally that extend from cementum of one tooth to the cementum of the neighboring tooth. Maintain relationship of adjacent teeth, protect interproximal bone. The transseptal fibers collectively form an interdental ligament connecting all the teeth of the arch. This ligament, although belonging to the supraalveolar fiber apparatus, appears to be uniquely important in maintaining the integrity of the dental arch. It is rapidly reformed after excision.
    zoom view
    Fig. 1.10: Gingival fibers
    11
    Residual portions of transseptal fibers are seen, even in advanced stages of resting periodontal disease.
  5. Dentoperiosteal group: On the oral and vestibular surfaces of jaws, dentoperiosteal group of fibers extends from the tooth, passing over the alveolar crest to blend with fibers of the periosteum of the alveolar bone. Anchors tooth to bone, protect periodontal ligament.
  6. Semicircular group: Group of fibers which attach at the proximal surface of a tooth, immediately below the cementoenamel junction, go around the facial or lingual marginal gingiva of the tooth and attach on the other proximal surface of the same tooth.
  7. Transgingival group: Fibers that attach in the proximal surface of one tooth, transverse the interdental space diagonally, go around the facial or lingual surface of the adjacent tooth, again traverse diagonally the interdental space and attach in the proximal surface of the next tooth. Secure alignment of teeth in the arch.
  8. Intergingival group: These fibers run parallel to dentition on vestibular and oral surfaces. They provide contour and support for the attached gingiva.
  9. Interpapillary group: They are seen in the interdental gingiva extending in a faciolingual direction. Provide support for interdental gingiva.
Dentogingival, dentoperiosteal and alveologingival fibers group provide the attachment of gingiva to the tooth and to the bony structure. Fibers of circular, semicircular, transgingival, intergingival and transseptal bundles connect teeth to one another.
 
Cells
  • Fibroblasts are derived from the undifferentiated progenitor mesenchymal cells that are present in the follicle. These are elongated or spindle shaped cells having prominent rough endoplasmic reticulum and golgi apparatus. Their cytoplasm is usually rich in mitochondria, vacuoles and vesicles. They play important role in the development, maintenance and repair of the gingival connective tissue. These cells have the ability to not only respond to paracrine as well as autocrine signals but also synthesize and secrete a number of growth factors, cytokines and metabolic products.
  • Mast cells are located perivascularly and are identified by their unique cytoplasmic granules which produce heparin and histamine.
  • Other cells are eosinophils, macrophages, adipose and inflammatory cells (neutrophils, plasma cells and lymphocytes).
 
Ground Substance
The cells, fibers, nerves and vessels of the gingiva are embedded in a viscous, gel-like ground substance. The ground substance is composed of proteoglycans and glycoproteins, which facilitates cell movement and diffusion of various biologically active substances. A number of proteoglycans have been identified in the gingival tissues including decorin, biglycan, versican and syndecan. Glycoproteins identified in gingival connective tissue are fibronectin, tenascin, osteonectin and laminin.
 
BLOOD SUPPLY
Arterial supply: Blood vessels are easily evidenced in tissue sections by means of immunohistochemical reactions. Earlier techniques like histoenzymatic reactions and perfusion with India ink into experimental animals techniques were used. There are three sources of blood supply to gingiva namely supraperiosteal arterioles, vessels of periodontal ligament and arterioles emerging from the crest of the interdental septa (Fig. 1.11). Supraperiosteal arterioles mainly supply free gingiva and gingival sulcus. These arterioles are the terminal branches of sublingual artery, mental artery, buccal artery, facial artery, greater palatine artery, infraorbital artery and posterior superior dental artery. Vessels of periodontal ligament mainly supply col area.
zoom view
Fig. 1.11: Gingival blood supply derives from: a. Periodontal ligament, b. Supraperiosteal vessels, c. Alveolar bone
12
Arterioles emerging from the crest of the interdental septa mainly supply attached gingiva.
Dentogingival plexus are plexus of blood vessels beneath junctional epithelium. The blood vessels in this plexus have a thickness of approximately 40 µm, which means that these are mainly venules. No capillary loops occur in it, in healthy gingiva. Subepithelial plexus are plexus of blood vessels beneath oral epithelium of free and attached gingiva, yield thin capillary loops of 7 µm to each connective tissue papilla.
The venous and lymphatic vessels follow a course closely paralleling that of arterial supply. Lymphatic drainage starts in the connective tissue papillae and drains into regional lymph nodes. Buccal gingiva of maxilla, buccal and lingual gingiva of mandibular premolar and molar region drains into submandibular lymph nodes. Mandibular incisor region drains into submental lymph nodes whereas third molars region drains into jugulodigastric lymph nodes. Their main function is to return fluids and filterable plasma components to the blood via the thoracic duct.
 
NERVE SUPPLY
The various regions of gingiva are innervated by end branches of trigeminal nerve. The gingiva on the labial aspect of maxillary incisors, canines, premolars is innervated by the superior labial branches from infraorbital nerve. Buccal gingiva in maxillary molar region is innervated by branches from posterior superior dental nerve. Palatal gingiva is innervated by greater palatal nerve except incisors area which is innervated by sphenopalatine nerve. Lingual gingiva in mandible is innervated by sublingual nerve, a branch of lingual nerve. Gingiva on the labial aspect of mandibular incisiors and canines is innervated by mental nerve. Buccal aspect of molars is innervated by buccal nerve. Innervations of mandibular premolars is by both mental and buccal nerve. In the attached gingiva, most nerves terminate within the lamina propria, and only a few endings occur between epithelial cells. Meissner type tactile corpuscles, krause type end bulbs and encapsulated spindles are the types of neural terminals.
 
CLINICAL CRITERIA OF NORMAL GINGIVA
 
Color
Color of the gingiva is described as coral pink which depends upon vascular supply, thickness of epithelium, degree of keratinization of epithelium and presence of pigment containing cells (Fig. 1.12).
zoom view
Fig. 1.12: Generalized melanin pigmentation
A variation in gingival pigmentation is not produced by variation in the number of pigment forming melanocytes but by genetically determined variation in their pigment producing capacity. Thus, variations in gingival pigmentation are related to complexion and race. It is lighter in blond individuals with a fair complexion than in dark complexioned individuals. In the Caucasian individuals pigmentation is minimal, in African or Asian individuals there are brown or blue- black areas of pigmentation while in Mediterranean people occasional patches of pigmentation are found.
Gingival pigmentation was classified according to modification of melanin index:
Category 0:
No pigmentation
Category 1:
Solitary unit(s) of pigmentation in papillary gingiva without formation of continuous ribbon between solitary units.
Category 2:
At least 1 unit of formation of continuous ribbon extending from two neighboring solitary units.
 
Surface Texture
The surface texture of free gingiva is smooth whereas of attached gingiva is stippled. Pitted surface texture giving orange peel appearance is called as stippling which is more prominent on the labial than on the lingual gingival surfaces. Stippling is normally present on attached gingiva and center of interdental papilla. It is best viewed by drying the gingiva and switching off the chair light. Stippling varies with age, it appears usually in children of about 5 years and increases with age but is absent in old age.
13
zoom view
Fig. 1.13: Stippling seen on attached gingiva and center of interdental papilla
Histologically: The bottom of the pits correspond to deep ridges or projections of epithelium into lamina propria of the connective tissue. The protruding parts correspond to thinner epithelium overridges or projections of the connective tissue. The ridge and the peg arrangements between the epithelium and connective tissue provide excellent mechanical stability between the two tissue components as well as large contact interphase for metabolic interchange. In erythematous tissue stippling may disappear, although it may be present in thick fibrotic tissue (Fig. 1.13), which is diseased. Stippling is not an absolute sign of health and the absence of it is not necessarily a sign of disease.
 
Contour
The marginal gingiva follows a scalloped outline normally and straight line along teeth with relatively flat surfaces. Attached gingiva has festooned appearance with intermittent prominence corresponding to contour of roots. When the teeth are placed more labially, then the normal arcuate contour is accentuated and gingiva is located farther apically. When teeth are lingually placed, the gingiva is horizontal and thickened. Thus, contour of gingiva depends upon shape and alignment of the teeth in the arch. It also depends upon the location and size of the area of proximal contacts and dimensions of the embrasures.
 
Shape
Shape of interdental gingiva depends upon contour of the proximal tooth surface, location and shape of the proximal contact and dimensions of the gingival embrasures. The interdental papilla is pointed and pyramidal in normal contact areas and in anterior regions. But it is flat or saddle shaped in spaced teeth and in molar regions.
 
Size
The size of the gingiva corresponds to the sum total of the bulk of cellular and intercellular elements and their vascular supply.
 
Consistency
On palpation with a blunt instrument, attached gingiva should be firm, resilient and tightly bound to the underlying hard tissues. The abundant collagen fibers and the non-collagenous protein combines to give gingiva, the firm consistency.
 
LANDMARK STUDIES RELATED
Ainamo A, Ainamo J. The width of attached gingiva on supraerupted teeth. Journal of Periodontal Research 1978;13:194–18.
This study comprised 28 first and second maxillary molars which in the lack of antagonists had erupted beyond the occlusal plane. The maxillary mucogingival junction was marked with short pieces of metal wires, orthopantograms were taken and the distance from the mucogingival junction to the floor of the nasal cavity and to the cementoenamel junction were measured to the nearest mm. Eleven measurable occluding contralateral teeth were used as controls. A comparison was also made between the supraerupted teeth and the previously measured normally occluding teeth. The results indicated that even during pronounced supraeruption, the teeth tend to erupt with their investing tissues while the location of the mucogingival junction remains constant. This finding is of special interest as it would make possible to treat the problem of a too narrow zone of attached gingiva by grinding the tooth out of occlusion and allowing it and its gingival margin to erupt. The anatomical width of attached gingiva, i.e. the distance from the mucogingival junction to the cementoenamel junction was found to be 3.7 mm wider in the supraerupted teeth than in the normal occluding control teeth.
Caffesse RG, Nasjleti CE, Castelli WA. The role of sulcular environment in controlling epithelial keratinization. Journal of Periodontology 1979; 50:1–6.
The influence of the sulcular environment on the keratinization of the outer surface gingival epithelium 14was tested in three young adult rhesus monkeys. A total of 40 mucoperiosteal flaps were raised and inverted so as to bring the outer surface epithelium in contact with the tooth and were sutured. The monkeys were sacrified after giving H3 thymidine one hour prior. The material was prepared for histologic and radioautographic evaluation. Results indicated that the outer surface epithelium changes its morphology to a nonkeratinized epithelium devoid of deep rete pegs when in close contact with the tooth, resulting in the anatomical characteristics normally seen in sulcular epithelium. It was concluded that the sulcular environment has the capability of controlling the keratinizing potential of the outer surface epithelium. The constant irritation of bacterial plaque and its product may be responsible for the premature desquamation of the sulcular epithelium which in turn might not allow its full differentiation.
 
POINTS TO PONDER
  • ✓ The junctional epithelium and gingival fibers together forms a functional unit called as dentogingival unit.
  • ✓ The pH of the gingiva ranges from 6.5 to 8.5.
  • ✓ Junctional epithelium is the only attachment in the body between soft tissue and a calcified tissue which is exposed to the external environment.
  • ✓ Gingival fiber groups enable the gingiva to form a rigid cuff around the tooth that add stability especially when a significant portion of the periodontal ligament and alveolar support is lost. This explains that the increased mobility in periodontally involved teeth immediately after surgical procedures is because these procedures disrupt or remove the gingival fiber groups.
 
BIBLIOGRAPHY
  1. Baktold PM, Walsh LJ, Narayanan AS. Molecular and cell biology of the gingiva. Periodontol 2000;24: 28–55.
  1. Eley BM, Manson JD. The periodontal tissues. In, Periodontics 5th ed Wright  2004; 1–20.
  1. Grant DA, Stern IB, Listgarten MA. Gingiva and dentogingival junction. In, Periodontics. 6th ed CV Mosby Company  1988; 25–55.
  1. Itoiz ME, Carranza FA. The Gingiva. In, Newman, Takei, Carranza. Clinical Periodontology. 9th ed WB Saunders  2003; 16–35.
  1. Lindhe J, Karring T, Araujo M. Anatomy of the Periodontium. In, Lindhe J, Karring T, Lang NP. Clinical Periodontology and Implant dentistry. 4th ed Blackwell Munksgaard  2003; 3–49.
  1. Ramfjord SP, Ash MM. Connective tissue. In, Periodontology and Periodontics, Modern Theory and Practice. 1st ed AITBS Publisher and distributor India,  1996; 15–20.
  1. Ramfjord SP, Ash MM. Epithelium. In, Periodontology and Periodontics, Modern Theory and Practice. 1st ed AITBS Publisher and distributor India,  1996; 5–14.
  1. Stern IB. Oral mucous membrane. In, Bhaskar SN. Orban's Oral histology and Embroylogy. 11th ed Mosby  1991; 260–336.
  1. Squier CA, Finkelstein. Oral mucosa. In, Tencate AR. Oral histology Development, Structure and Function. 5th ed Mosby  1998; 345–87.
 
MCQs
  1. The mucogingival junction is located between the:
    1. Free gingiva and attached gingiva
    2. Free gingiva and tooth
    3. Base of the sulcus and alveolar mucosa
    4. Attached gingiva and alveolar mucosa
  1. Stippling is seen in:
    1. Marginal gingiva
    2. Attached gingiva
    3. Interdental gingiva
    4. Attached gingiva and center of interdental papilla
  1. The area of periodontium more susceptible to tissue breakdown is:
    1. Free gingiva
    2. Gingival sulcus
    3. Interdental col
    4. Interdental papilla
  1. Dentogingival unit comprises:
    1. Gingival fibers
    2. Gingival fibers and junctional epithelium
    3. Periodontal fibers and ligament
    4. None of the above
  1. Gingiva is supplied by:
    1. Supraperiosteal vessels
    2. Vessels of periodontal liagment
    3. Arterioles emerging from alveolar crest
    4. All of the above
  1. Which of the following fiber group is not attached to alveolar bone:
    1. Transseptal fibers
    2. Oblique fibers
    3. Horizontal fibers
    4. Dentoperiosteal fibers
      15
  1. Odland bodies are:
    1. Modified mitochondria
    2. Modified lysosomes
    3. Modified ribosome
    4. Modified centrioles
  1. Which of the following cells of the gingival epithelium is not a clear cell?
    1. Keratinocyte
    2. Langerhans cell
    3. Merkel cells
    4. Melanocytes
  1. The length of the junctional epithelium ranges from:
    1. 0.25 – 0.75 mm
    2. 0.15 – 0.75 mm
    3. 0.25 – 1.35 mm
    4. 0.5 – 1.0 mm
  1. The width of attached gingiva is greatest in:
    1. Maxillary anterior region
    2. Maxillary molar region
    3. Maxillary premolar region
    4. Mandibular premolar region
  1. The color of attached gingiva in health, is determined by:
    1. The presence of melanophores
    2. Degree of keratinization of epithelium
    3. Vascular supply
    4. All of the above
  1. If a diastema is present, the interdental papilla is:
    1. Larger in size
    2. Smaller in size
    3. Absent in the region
    4. None of the above
  1. Which of the following enzymes increase their activity towards surface in gingival oral epithelium?
    1. Succinic dehydrogenase
    2. Nicotinamide adenine dinucleotide
    3. Cytochrome oxidase
    4. Glucose-6-phosphatase
Answers
1. D
2. D
3. C
4. B
5. D
6. A
7. B
8. A
9. C
10. A
11. D
12. C
13. D