periodontal diseases: effects on diabetes control and ... · periodontal infection and...
TRANSCRIPT
![Page 1: Periodontal Diseases: Effects on Diabetes Control and ... · Periodontal infection and complications of diabetes Thorstensson et al., 1996; J Clin Periodontol. 39 case-control pairs,](https://reader034.vdocuments.site/reader034/viewer/2022042309/5ed6d173c7a5935b07521fd1/html5/thumbnails/1.jpg)
Periodontal Diseases: Effects on
Diabetes Control and Complications
Clinical Directors Network-Community Health Centers-University of Michigan School of Dentistry Collaboration
October 16-18, 2006
G.W. Taylor, W.S. Borgnakke, M.C. Manz
University of Michigan School of Dentistry
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Overview Overview of diabetes and periodontal diseases
Conceptual model of chronic periodontal inflammation and insulin resistance
Periodontal infection and insulin resistance: empirical evidence
Periodontal infection and glycemic control: empirical evidence
Observational studies
Treatment studies
Significance of improving glycemic control
Periodontitis and complications of diabetes
Current collaboration with CDN and CHC’s
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Diabetes Mellitus
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Type 15-10%
Type 290-95%
Gestational2-5%
Other1-2%
Insulin: action, production, or both
Hyperglycemia and other and metabolic abnormalities
Chronic ComplicationsAtherosclerosis NeuropathyRetinopathy Perio diseasesNephropathy Impaired wound healing
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Diabetes Overview
Prevalence: 20.8 mil; 7.0% of U.S. pop.
Diagnosed: 14.6 mil
Undiagnosed: 6.2 mil
Incidence: 1,300,000 /yr
Prevalence by age
60+: 20.9%
20+: 9.6%
<20: 0.22%
Source: http://www.cdc.gov/diabetes/pubs/estimates05.htm#fig2, Feb, 2006
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Diabetes Overview (con’t.)
Prevalence by race/ethnicity (20 yrs+)
Non-Hispanic whites: 8.7%
Non-Hispanic blacks: 13.3%
Hispanic/Latino Americans: 9.5%
Native Amer. and Alaska Natives: 15.1%
Asian Amer. & Pacific Islanders: up to 2.5x nHwhite
http://www.cdc.gov/diabetes/pubs/estimates05.htm#fig2, Feb, 2006
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Age-Standardized Prevalence of Diagnosed Diabetes
per 100 Adult Population, by State, United States
1994 2003
Source: http://www.cdc.gov/diabetes/statistics/prev/state/fPrev1994and2003.htm
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What is periodontal disease?
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Periodontal disease
Chronic inflammatory disease
Bacterial etiology
Gram negative anaerobes are prominent
Destruction of periodontal tissues
Formation of pathologic pockets around teeth
Loss of connective tissue attachment
Loss of alveolar bone
Can lead to tooth loss
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Gingivitis
Bacterial plaque
Initial periodontal disease
Inflamed gingiva
Reversible
Can progress if untreated
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Periodontitis
Bacterial plaque
Advanced periodontal disease
Connective tissue loss
Periodontal ligament loss
Supporting bone loss
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Measuring periodontal status
Clinical Radiographic
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How prevalent is periodontal disase?
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Gingivitis and severe periodontal disease prevalence (1+ sites with LPA 6+ mm)
18-24 25-34 35-44 45-54 55-64 65-74 75+
5854
4853 53
5655
0 3 714
19
30
23
0
10
20
30
40
50
60
Pe
rce
nt
AGE
LPA6mm+
Gingivitis
Source: NHANES 3 (1989-94), US Population
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Severe Periodontitis by race/ethnicity:U.S. population (attachment loss > 6mm)
25
12
1721
28
1
5
12
24
3438
56
1 1
6
19
26
36
40
00
10
20
30
40
50
60
18-24 25-34 35-44 45-54 55-64 65-74 75+
AGE
Pre
vale
nce
(%
)
NHW
NHB
MA
Source: NHANES III (1989-94), US Population
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Diabetes and periodontal health
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%Children and adolescents with 1+ sites with periodontal attachment loss ≥ 2mm. (Lalla E et al. 2006)
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Incidence of Alveolar Bone Loss after ~2 yrs Follow-up in the Pima Indians
Source: Taylor et al., 1998
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Why do we think periodontal disease
can have an adverse effect on
glycemic control?
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Periodontitis and Chronic Systemic Inflammation
Relationship to Insulin Resistance
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Fatty acidsFMLPLPS
IL-8
Response to Bacterial Plaque in Disease
LowIL-10TGF-bIL-1raTIMPs
HighTNFαIL-6
IL-1βIFN-gPGE2MMPs
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Chronic inflammationVisceral obesity
Proinflammatory stateChronic overexpression of cytokines
Insulin resistance
Pancreatic beta cell damage
GlycemicControl
TNF
Liver
Acute Phase Response (CRP, Fibrinog., PAI-1)
Il-6
Conceptual Model: From Richard Donahue, 2004
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What empirical evidence do we have
to link periodontal disease to insulin
resistance and glycemic control?
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Supporting epidemiologic evidence:cross-sectional and longitudinal studies
Inflammation and insulin resistance
Insulin resistance and diabetes
Inflammation and diabetes
Periodontitis and the acute-phase response
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Periodontitis and Insulin Resistance: Epidemiologic Evidence of an Association
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To evaluate the association between severe periodontitis and insulin resistance in a representative sample of U.S. adults, ages 17-90 years old.
Periodontitis and Insulin Resistance in U. S. Adults, NHANES III, Preliminary
Results
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MAJOR EXPOSURE
Severe periodontitis
At least 1 site with 6 mm or more of attachment loss
&
Gingival bleeding at the teeth with 6+ mm of attachment loss
OUTCOME
Insulin ResistanceHOMA formula
Fasting insulin (FI)Fasting glucose (FG)
FI x FG22.5
Dichotomous variable using the 80th
percentile as the cutpoint
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Prevalence of insulin resistance in U.S. non-smoking adults, ages 17+, by periodontal status* (N=5313)
61
25
39
75
0
10
20
30
40
50
60
70
80
No Sev. PerioDz n=5032 Sev. PerioDZ n=281
Periodontal Disease Status
% o
f P
ers
on
sNo Insulin Resistance
Insulin Resistance
Source: NHANES III (1989-94), US Population
* Sev. PerioDz=1+ site w LPA 6 mm+, gingival bleeding
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Association between severe periodontitis and insulin resistance (HOMA 80th ): crude odds ratio
Total study group: N=5313 individuals
Severe periodontitis: n=281 (5.3%)
Insulin resistanceNo severe periodontitis: n=1474 (24.6%)
Severe periodontitis: n=100 (38.7%)
ASSOCIATION: Crude Odds Ratio: 2.3 (1.58, 3.39)
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Logistic regression model Response: HOMA 80th (n=1574/5313)
COVARIATE OR 95% CI
Severe perio. 1.74 1.01, 3.0
BMI (>27) 4.77 4.1, 5.6
HDL (≤40) 2.2 1.7, 2.9
TRIG (>200) 2.7 2.0, 3.6
CRP 1.3 1.1, 1.5
Diabetes 4.72 2.6, 8.4
Other covariates controlled in model were age,race/ethnicity, exercise, white blood cell count, fibrinogen.
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Periodontal Infection Its Effect on Glycemic Control:
Observational Studies
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Epidemiologic Evidence: Incidence of poor glycem. control at ~2-yr follow-up in the Pima Indians
N for bone loss < 50% = 56N for bone loss 50%+ =49Source: Taylor et al., 1996
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Prevalence of poorer glycemic control in U.S. adults, ages 45+, by periodontal status*
4139
5961
0
10
20
30
40
50
60
70
No Sev. Perio. Sev. Perio
Periodontal Disease Status
% o
f P
ers
on
sBetter control: n=309
Poorer control: n=226
Source: NHANES III (1989-94), US Population
* Sev. Perio=1+ site w LPA 6 mm+, gingival bleeding
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Association between severe periodontitis and glycemic control: N=535
Crude Odds Ratio: 3.20 (1.47, 6.98)
Glycemic Control
Periodontal Status Better
HbA1c < 8%
Poorer
HbA1c ≥ 8%
Sev. Perio: NO 270 (61%) 170 (39%)
Sev. Perio: YES 39 (41%) 56 (59%)
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Logistic regression model: poor glycemic control in U.S. adults, ages 45+, non-smoking, NHANES III
COVARIATE OR 95% CI
Severe perio. 4.9 2.0, 11.9
Taking Diab med 3.4 1.7, 5.8
BMI (≥ 27) 2.6 1.2, 5.4
TRIG (>200) 2.7 2.0, 3.6
CRP (>1.0) 2.6 0.5, 13.8
Exercise 1.0 0.99, 1.01
Other covariates controlled in model were age,race/ethnicity, sex, education, poverty income ratio, and MD and DDS visits.
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Periodontal Infection Its Effect on Glycemic Control:
Non-surgical Periodontal
Treatment Studies
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Locations of clinical therapeutic studies
N
EW
S
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Non-surgical periodontal therapy studies: organizing the evidence AKA “sorting the apples
and oranges”
Randomized clinical trials (RCT)
Non-treated control group: 1 positive/3 studies
Positive control group: 3 positive/3 studies
Non-randomized clinical treatment studies (non-
RCT)
Non-treated control group: 1 positive/2 studies
No control group: 5 positive/8 studies
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Non-surgical periodontal therapy: a meta-analysis. Janket et al. J Dent Res, 2005
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Treating Periodontal Infection: Effects on Glycemic Control
University of Michigan
SUNY at Buffalo
University of North Carolina at Chapel Hill
NIH/NIDCR
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Study Design
Group 1
Group 2
3 60 9 12 15
3 60 9 12 15
month
month
Perio tx + Doxy.
Perio tx + Metron.
SPT SPT SPT SPT
SPT SPTSPTSPT
Controls3 60 9 12 15month
Prophy + Placebo. Perio tx.
ssrt ssrtssrt
SPT= supportive periodontal therapy, including ssrtssrt= site specific rescue therapy
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Preliminary results: Improvement in Hemoglobin A1c N=16, 15, 15
-1
-0.8
-0.6
-0.4
-0.2
0
0.2
dhb_tx3 dhb_tx6 dhb_tx9 dhb_tx12 dhb_tx15
Visit: months of follow-up after treatment
Hb
A1c d
iffe
ren
ce f
rom
tx v
isit
delay
doxy
metro
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Study Design
Group 1
Group 2
3 60 9 12 15
3 60 9 12 15
month
month
Perio tx + Doxy.
Perio tx + Metron.
SPT SPT SPT SPT
SPT SPTSPTSPT
Controls3 60 9 12 15month
Prophy + Placebo. Perio tx.
ssrt ssrtssrt
SPT= supportive periodontal therapy, including ssrtssrt= site specific rescue therapy
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Overview
Global overview of diabetes and periodontal diseases prevalence
Conceptual model of chronic periodontal inflammation and insulin resistance
Periodontal infection and glycemic control
Observational studies
Treatment studies
Significance of improving glycemic control
Periodontitis and complications of diabetes
Conclusions
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Significance of improving of glycemic control
Any sustained lowering of blood glucose helps delay the onset and progression of microvascular complications of diabetes
Medical complications of diabetes Neuropathy – 50% Any cardiovascular disease – 38% Coronary heart disease – 22% Stroke – 21% Visual Impairment – 23% Kidney disease – 40% of new cases of renal failure due to
diabetes
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Landmark clinical trials demonstrating the significance of improving of glycemic control
Diabetes Control and Complications Trial (DCCT)
Intensive blood glucose control in type 1 diabetes
35% to 70% reduction in risk of retinopathy, nephropathy and neuropathy
UK Prospective Diabetes Study (UKPDS)
Intensive blood glucose control in type 2 diabetes
12% to 33% reduction in risk of retinopathy and nephropathy
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Periodontal infection and complications of diabetes
Thorstensson et al., 1996; J Clin Periodontol.
39 case-control pairs, type 1 and type 2 diabetes
Cases (severe periodontal disease) had greater risk for Proteinuria
Cardiovascular complications: stroke, TIA, angina, myocardial infarction, and intermettent claudication
Saremi et al., 2005; Diabetes Care.
Prospective cohort study of n=628, type 2 diabetes
Severe periodontal disease: 3.2x greater risk for cardiorenal mortality (ischemic heart disease and nephropathy)
Controlled for established risk factors: age, sex, duration, BMI, hypertension, blood glucose, cholesterol, ECG abnormalities, macroalbuminuria, and smoking
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Conclusions
Evidence that treating periodontal infection can:
Lead to improved glycemic control
Possibly prevent, delay, or reduce severity of complications
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TREATING PERIODONTAL INFECTION: EFFECTS ON GLYCEMIC CONTROL IN
COMMUNITY HEALTH CENTERS
Our Collaboration, funded by NIH/NIDCR
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Specific Aims
1. Identify and characterize the population of patients with type 2 diabetes, ages 18+ years, who are listed in the diabetes registry
2. Select a probability sample (n=200) from each center’s list to review medical and dental records and the CHC’s electronic databases to determine the degree to which information is available and accessible for assessing eligibility
3. Test feasible mechanisms of contacting potential study participants, including telephone, U.S. mail, and face-to-face contact in the medical and dental departments of the CHCs to determine study eligibility and willingness to participate in a clinical examination and interview session, and the yet-to-be planned full-scale RCT
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Specific Aims, con’t.
4. Determine proportion of the 50 sampled patients from each Center who will present for a clinical examination and interview session
5. Characterize the patients who present for the dental appointment with regards to:
a. meeting the clinical periodontal disease and medical eligibility criteria,
b. responses to a set of self-report questions designed to estimate periodontal disease status,
c. willingness to participate in the full-scale RCT, and d. other characteristics influencing periodontal disease status
and glycemic control status, including current HbA1c status.
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Inclusion criteria
18+ years old
Registered patient at one of the four participating CHCs
Type 2 diabetes, at least 6 months duration
At least 6 natural teeth
Willingness to participate in the pilot clinical examination and interview session
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Exclusion criteria
Blood dyscrasias
Pregnancy or breast feeding
Presence of severe cognitive or communicative impairment
HIV+ positive
Cardiac pacemaker
Requiring prophylactic antibiotics before dental treatment
Medically unstable
{(e.g. accelerated angina, undergoing medical diagnostic evaluation, and current or recent severe illness or surgery (e.g. end-stage renal disease or terminal cancer)}
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Diabetes registry
Ages 18; N=all w/ dm 6mosOther data sources for dx and
procedure info (ICD9, PECs)
Initial CHC data base.
Send to UM
UM eval. elig., selects strat. sample
N=200, List 1
UM prioritizes for contacting
Study intro letter sent to List 1
CDN contacts List 1: recruitm. script,
track contacts, schedule appointment. n=50/clinic
Review medical records for excl. criteria
Consent visit and, if at all possible, study visit: n=50/clinic
Dental records
Review???
Age, gender,
Race/ethn, HbA1c,
ICD 9 exclus. criteria
Other med condition info.
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Informed consent
Study visit
Screening interview (screening
form and script
Brief Phys. Exam:
Ht.
Wt.
BP
HbA1c
Interview Dental exam:
EO &IO soft tissue
# teeth
Caries status
Perio (Pck, BOP)
Participant
Advise and
$25 pymt
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Outcomes anticipated for our project
Evaluation of feasibility of conducting randomized clinical trial (RCT)
Prelim data for planning grant (R-21) to plan multi-center RCT (Feb 1 or June 1, 2007 submission)
Prelim data for multi-center RCT proposal (U-01)
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University of Michigan School of Dentistry
Please feel to contact me:
George W. Taylor, DMD, DrPH
Thank you for your attention