lecture 8 effect of systemic ds on periodontal ds Flashcards

1
Q

what type of periodontitis for major impact

A

severe/early-onset periodontitis

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2
Q

what type of periodontitis for moderate impact?

A
  • chronic periodontitis
  • increase prevalance
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3
Q

systemic disorders cause –>

A

loss of periodontal tissue

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4
Q

what three things can influence periodontal inflammation

A
  • genetic disorder
  • acquired immunodeficiency ds
  • inflammatory ds
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5
Q

what ds is associated with this oral presentation

A
  • oral presentation of Down Syndrome
  • moderate to severe periodontitis with rapid progression
  • local factors do not explain the severity of the periodontal destruction
  • intrinsic immune system defects
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6
Q

explain what leukocyte adheesion deficiency is

A
  • a mutation in beta-2 integrin gene where there is a lack of them in leukocytes.
  • This causes for low integrin expression on the neutrophils so
  • neutrophils are confined to blood vessels (loose neutrophil-associated homeostasis)
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7
Q

oral manifestations seen in LAD

A
  • severe gingial inflammation, acute gingival lesions
  • early-onset and rapidly progressive alveolar bone loss
  • early loss of the primary AND perm teeth

*not just oral but history of recurrent inection but with no pus

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8
Q

what ds is this oral presentation associated with?

A

LAD leukocyte adhesion deficiency

  • severe gingial inflammation, acute gingival lesions
  • early-onset and rapidly progressive alveolar bone loss
  • early loss of the primary AND perm teeth
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9
Q

describe papillon-lefevre syndrome

A

mutations in the cathepsin C gene which can compromise neutrophil function

can have hyperkeratotic lesions

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10
Q

if we have a pt with hyperkeratotic lesions on palms, soles of feet, elbow and/or knees with periodontal inflammation what could it be

A

papillon-lefevre syndroms

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11
Q

oral presentation of papillon-lefevre

A
  • severe gingival inflammation
  • early-onset and rapidly progressive alveolar bone loss
  • early loss of the primary and permanent teeth
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12
Q

describe chediak-higashi syndrome

A
  • a mutation in gene (CHS1 and LYST) which can cause albinism, pyogenic infections, and varying neurologic problems
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13
Q

some clinical S&S of Chediak-Higashi Syndrome

A
  • partial oculocutaneous albinism which can cause defects in melanin granules
  • recurrent pyogenic infections
  • varying neurologic probs like intellectual deficit and dementia
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14
Q

oral manifestations seen in Chediak-higashi Syndrome

A
  • severe gingival inflammation
  • Early-onset and rapidly progressive alveolar bone loss
  • Early loss of the primary and perm teeth
  • Poor response to dental tx
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15
Q

describe congenital neutropenia

A

Mutations in ELANE (50%), HAX1 (10%) gene.

A decrease # and dysfunction of neutrophils, and defficient in immune response so lots of severe and recurrent infections

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16
Q

what are the ds associatd with immunologic disoders

A
  1. Down syndrome
  2. LAD
  3. Papillon Lefevre
  4. Chediak-higashi syndrome
  5. Congenital neutropenia
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17
Q

what are the ds affecting the oral mucosa and gingival tissue

A
  1. epidermolysis bullosa
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18
Q

describe epidermolysis bullosa

A

aka Kindler Syndrome

a mutation in the fermitin family homologue 1 gene.

Has a lack of integrin activiation which affects the keratinocyte cell adhesion which can lead to defects in basement membrane zones as well.

Recurrent blister formation

Photosensitivity

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19
Q

oral manifestations of epidermolysis bullosa

A

oral blisters, severe periodontitis, and you need immunofluorescence to confirm dx

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20
Q

what are the ds affecting the CT

A
  1. ehlers danlos syndrome
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21
Q

describe ehlers-danlos syndrome

A

a mutation in genes encoding fibrillar collagens or enzymes in the biosynth

it affects collegen production and composition so pts will have joint hypermobility, skin extensibility and tissue fragility

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22
Q

oral manfestations of ehlers-danlos syndrome

A
  • generalized, early onset severe periodontitis and gingival recession
  • early loss of primary and perm teeth
23
Q

what are the metabolic and endocrine disorders

A
  1. hypophosphatasia
  2. DM
  3. Obesity
  4. Osteoporosis
  5. Acquired Immunodeficiency ds
  6. Inflammatory ds
  7. Epidermolysis Bullosa Acquisita
  8. Inflammatory bowel ds
  9. Rhemuatoid arthritis
24
Q

describe Hypophosphatasia

A

lack of phosphate in the body. ALPL gene mutation.

so you have defective cementums, alveolar bone loss and premature loss of teeth

25
oral manifestations of Hypophosphatasia
- impaired bone/tooth mineralization - defects in root cementum
26
describe DM
disorder of glucose metabolism there is an accumulation of AGEs There are two types 1 and 2.
27
oral manifestations of DM
- increased prevalence and severity of attachment loss and multiple periodontal abscess - RED gingiva
28
relationship between DM and periodontal ds
DM is a risk factor for periodontal ds BUT periodontal ds is also a complicating factor for DM. Periodontitis also affects glycemic control.
29
relationship between obesity and periodontitis
it is a 2 way relationship
30
obesity can cause an elevated \_\_\_\_
synthesis of inflammatory cytokines (TNF, IL-1, IL-6) these can then cause chronic ds
31
describe osteoporosis
due to lack of estrogen (withdrawals) it can stimulate osteoclasts and decreases bone mineral density.
32
estrogen and inflammtion shared risk factors
age, vitamin D and calcium deficiency, smoking
33
what are the Acquired immunodeficiency ds
1. acquired neutropenia 2. HIV infection
34
describe aquired neutropenia
due to a decreased production or increased destruction of granulocytes so pt has increase irks for infections and periodontitis correclty with severety of neutropenia
35
describe HIV infection
deficiency of the immune system due to infection with the HIV virus increase risk for infections, neosplasms (kaposi sarcoma)
36
what are the inflammatory diseases
Epidermyloysis bullosa acquisita Inflammatory bowel ds Rheumatoid arthritis all of these are autoimmune ds
37
describe epidermolysis bullosa acquisita
a pathogenic autoantibodies bind to target antigens. two types: inflammatory form and mehcanobullous types
38
oral manifestations of epidermolysis bullosa acquisita
- Generalized gingival inflammation. Severe alveolar bone loss. Recurrent blister formation. Immunoflourescence on basment membrane - split skin.
39
describe inflammatory bowel ds
it is a hypersensitivity of immune responses with microbiological, host and environmenetal determinants.
40
describe rheumatoid arthritis
a chronic auto-inflammatory ds - increased risk for loss of periodontal attachment, alveolar bone there is a biological link between rhematoid arthritis and periodontits.
41
stress/anxiety/depression/negative life event causes what cascade
increase serum cortisol (activates limbic-hypothalamic-pituitary-adrenal axis) --\> immune system depression --\> change in behavior/mood/physiological markers risk facotrs for necrotitizng peridontal ds
42
smoking caues what cycle
impaired immune system --\> subgingival anaerobic infection --\> connective tissue cytotoxicity --\> imparied wound healing --\> increased severity of periodontal ds --\> impaired immune system
43
chronic nicotine exposure process
chronic nicotine exposure --\> impairment of antigen-mediated T cell signaling --\> inhibits antibody-forming cell response --\> immunosupreesion.
44
smoking (nicotine and tars) cause what
overal a decrease tissue oxygenation which cauess **subgingival anerobic infection, CT cytotoxicity and impaired wound healing**
45
chronicity = what effetcs
fibrotic
46
what are bisphosphonates
- function to inhibit osteoclast activity - they treat cancer (IV administration), treat osteoporosis (oral administration) and inhibit osteoclast activity and interfere with bone turnover
47
neoplasms that have independent etiology to loss of peridontal tissue
oral squamous cell carcinoma odontogenic tumors other primary neoplasms of periodontal tissue secondary netastatic neoplasms of periodontal tissue
48
other disorders that have independent etiology to loss of peridontal tissue
langerhans cell histiocytosis
49
what is langerhans cell histiocytosis
has peripheral small vessel necrotizing vasculitis, respiratory and renal impairment, characterisitic fiery and hyperplastic gingival inflammation and alveolar bone loss
50
describe giant cell granuloma
a reactive proliferation, beningn lesion with no systemic features. peripheral giant cell granuloma - gingiva only. gingival swelling and some loss of periodontal tissue central giant cell granuloma - loss of periodontal supporting tissue, may extend toward marginal periodontal tissue
51
oral manifestations of hyperparathyroidism
widening of pdl, single/multiple osteolytic lesions in the jaw that mimic peridontal bone loss (brown tumors)
52
what is scleroderma
autoimmune ds of the CT with many different systemic presentations
53
oral manifestations of scleroderma
widening pdl, and higher prevalence of periodontitis