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Department of Epidemiology and Biostatistics (A.V.S., E.V., L.P.) and Division of Endocrinology (D.E.S., K.R.F.), Department of Medicine, University of California, San Francisco, San Francisco, California 94107-1762; Department of Geriatrics (B.L.-C.), Reynolds Institute on Aging, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72202; Department of Epidemiology (E.S.S., S.W.P.), Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania 15260; Department of Epidemiology (H.E.R.), MedStar Research Institute, Hyattsville, Maryland 20785; Division of Rheumatology (L.C.), Department of Medicine, University of Tennessee, Memphis, Tennessee 38163; Department of Medicine (B.A.B.), Johns Hopkins University, Baltimore, Maryland 21205; Department of Medicine (S.W.P.), Pochon CHA University, Seoul 135-081 Korea; Department of Medicine (N.E.L.), University of California, Davis, Sacramento, California 95616; Laboratory of Epidemiology, Demography, and Biometry (T.B.H.), National Institute on Aging, Bethesda, Maryland 20892; and Research Institute (S.R.C.), California Pacific Medical Center, San Francisco, California 94120
Address all correspondence and requests for reprints to: Ann V. Schwartz, Ph.D., Department of Epidemiology and Biostatistics, University of California, San Francisco, 185 Berry Street, Lobby 4, Suite 5700, San Francisco, California 94107-1762. E-mail: aschwartz{at}psg.ucsf.edu.
Context: Activation of peroxisome proliferator-activated receptor-
by thiazolidinediones (TZDs) results in lower bone mass in mice.
Objective: The objective of the study was to determine whether TZD use is associated with changes in bone mineral density (BMD) in older adults with type 2 diabetes.
Design: We analyzed 4-yr follow-up data from the Health, Aging, and Body Composition observational study.
Setting: The study was conducted in a general community.
Patients: White and black, physically able men and women, aged 7079 yr at baseline with diabetes defined by self-report, use of hypoglycemic medication, elevated fasting glucose (
126 mg/dl), or elevated 2-h glucose tolerance test (
200 mg/dl) participated in the study.
Main Outcome Measures: Whole-body, lumbar spine (derived from whole body), and hip BMD were measured by dual-energy x-ray absorptiometry at 2-yr intervals.
Results: Of 666 diabetic participants, 69 reported TZD use at an annual visit, including troglitazone (n = 22), pioglitazone (n = 30), and/or rosiglitazone (n = 31). Those with TZD use had higher baseline hemoglobin A1c and less weight loss over 4 yr but similar baseline BMD and weight than others with diabetes. In repeated-measures models adjusted for potential confounders associated with TZD use and BMD, each year of TZD use was associated with greater bone loss at the whole body [additional loss of 0.61% per year; 95% confidence interval (CI) 1.02, 0.21% per year], lumbar spine (1.23% per year; 95% CI 2.06, 0.40% per year), and trochanter (0.65% per year; 95% CI 1.18, 0.12% per year) in women, but not men, with diabetes.
Conclusion: These observational results suggest that TZDs may cause bone loss in older women. These results need to be tested in a randomized trial.
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