Periodontitis as Manifestation of Systemic Disease Flashcards
Disorder of glucose metabolism
Accumulation of AGEs AGEs - RAGE (Receptor of AGEs) interaction
Chronic status of elevated blood glucose level
Diabetes mellitus
Early onset 5-10% of cases Destruction of beta cells Absolute insulin deficiency Marked tendency toward ketosis and coma
Type 1 DM
Adult onset
90-95% of cases
Obesity is a factor
Blood level of insulin is normal, increased or decreased
Development of ketosis and coma is uncommon
Type 2 DM
______as a risk factor for periodontal disease
-Increased prevalence and severity of attachment loss
Multiple periodontal abscess
Diabetes
Periodontitis ALSO affects ______ in relation to DM
glycemic control
What occurs when a pt is obese that causes more systemic effects?
State of low grade inflammation
Trisomy 21 or mongolism
Characteristic physical appearance
Mental deficiency and growth retardation
Down syndrome
Moderate to severe periodontitis with rapid progression
Local factors alone failed to explain the severity of
periodontal destruction
Intrinsic immune system defects Poor PMN chemotaxis, phagocytosis, intracellular killing
Down syndrome
Mutation in beta-2 integrin (ITGB2) gene Lack of beta-2 integrin mRNA in leukocytes
Low integrin (CD18 or CD15) expression on neutrophils
Neutrophils are confined to blood vessels Disruption of neutrophil-associated homeostasis
History of severe recurrent infection but no pus Leukocytosis is common
Severe gingival inflammation, acute gingival lesions
Early-onset and rapidly progressive alveolar bone loss
Early loss of the primary and permanent teeth
– Seen in Down Syndrome too
Leukocyte Adhesion Deficiency
Mutations in the cathepsin C gene (CTSC) Chromosome 11q14
Compromised neutrophil function Decreased phagocytosis (Rathi, 2002)
Hyperkeratotic lesions Palms, soles of the feet, elbows, knees
Severe gingival inflammation
Early-onset and rapidly progressive alveolar bone loss
Early loss of the primary and permanent teeth
Papillon–Lefèvre
Syndrome
Mutations in CHS1, LYST gene Lysosomal trafficking defect
Partial oculocutaneous albinism Defects in melanin granules
Recurrent pyogenic infections Circulating leukocytes exhibit defective lysosomes
Decrease in phagocytosis
Varying neurologic problems Intellectual deficit and dementia
Severe gingival inflammation
Early-onset and rapidly progressive alveolar bone loss
Early loss of the primary and permanent teeth
Poor response to dental treatment
Chediak-Higashi Syndrome
Mutations in the ELANE (50%), HAX1(10%) gene 1/3 causes remain unknown
Decrease in number of neutrophils ANC < 500 cell/uL and static
Deficiency in the immune response Severe and recurrent infections
Severe periodontitis is common
Higher risk for tooth loss
Oral ulcers
Congenital Neutropenia
For the genetic systemic diseases, when is the onset of periodontitis?
Early onset
For the genetic systemic diseases, does dental tx help the prognosis of perio tooth loss?
Not effectively in most cases
Which of the following statement is incorrect?
A. Periodontitis as a manifestation of a systemic disease is defined
by influencing the course of periodontitis.
B. Periodontitis as a manifestation of a systemic disease is defined
by affecting the periodontal supporting tissues independently of
dental plaque biofilm‐induced inflammation
C. Acquired immunodeficiency diseases have a major impact on the
loss of periodontal tissue by influencing periodontal inflammation
D. Genetic disorders having a impact on the loss periodontal tissue
are related to early-onset periodontitis
B. Periodontitis as a manifestation of a systemic disease is defined
by affecting the periodontal supporting tissues independently of
dental plaque biofilm‐induced inflammation
Mutation in the fermitin family homologue 1 gene (kindlin-1; FERMT1)
Lack of integrin activation Affect keratinocyte cell adhesion
Lead to molecular defects in basement membrane zone
Photosensitivity
Recurrent blister formation
Oral blisters formation
Severe periodontitis Alveolar bone loss that progress rapidly
Need immunofluorescence to confirm diagnosis Skin biopsy of an included blister
Epidermolysis Bullosa / Kindler syndrome