Antiretroviral therapy and the prevalence and incidence of diabetes mellitus in the Multicenter AIDS Cohort Study

被引:635
作者
Brown, TT
Cole, SR
Li, XH
Kingsley, LA
Palella, FJ
Riddler, SA
Visscher, BR
Margolick, JB
Dobs, AS
机构
[1] Johns Hopkins Univ, Dept Med, Sch Med, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Dept Epidemiol, Bloomberg Sch Publ Hlth, Baltimore, MD 21218 USA
[3] Univ Pittsburgh, Sch Publ Hlth, Dept Epidemiol, Pittsburgh, PA 15260 USA
[4] Univ Pittsburgh, Sch Med, Dept Med, Pittsburgh, PA 15260 USA
[5] Northwestern Univ, Feinberg Sch Med, Dept Med, Chicago, IL 60611 USA
[6] Univ Calif Los Angeles, Sch Publ Hlth, Dept Epidemiol, Los Angeles, CA 90024 USA
关键词
D O I
10.1001/archinte.165.10.1179
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Background: The risk of diabetes mellitus (DM) in human immunodeficiency virus (HIV)-infected patients receiving highly active antiretroviral therapy (HAART) has not been well defined. Methods: We conducted an analysis in the Multicenter AIDS Cohort Study to determine the prevalence and incidence of DM in this cohort of HIV-infected and HIV-seronegative men. Prevalence analysis included 1278 men (710 HIV seronegative and 568 HIV infected, 411 receiving HAART) with fasting glucose concentration determinations at baseline. Incidence analysis included 680 of these 1278 men who at the baseline visit had a fasting glucose concentration of 98 mg/dL (5.4 mmol/L) or less, no self-reported history of DM, and no self-reported use of antidiabetic medication. Diabetes mellitus was defined as a fasting glucose concentration of 126 mg/dL (7 mmol/L) or higher, self-reported diagnosis of DM, or self-reported use of antidiabetic medication. Results: Fifty-seven (14%) of the 411 HIV-infected men using HAART at the baseline visit had prevalent DM compared with 33 (5%) of the 711 HIV-seronegative men (prevalence ratio=4.6; 95% confidence interval, 3.0-7.1, adjusted for age and body mass index [calculated as weight in kilograms divided by the square of height in meters]). The rate of incident DM was 4.7 cases per 100 person-years among HIV-infected men using HAART compared with 1.4 cases per 100 person-years among HIV-seronegative men (rate ratio = 4.11; 95% confidence interval, 1.85-9.16, adjusted for age and body mass index), during the 4-year observation period, based on a median follow-up of 2.3 years. Conclusion: The incidence of DM in HIV-infected men with HAART exposure was greater than 4 times that of HIV-seronegative men, representing a risk that is higher than previous estimates.
引用
收藏
页码:1179 / 1184
页数:6
相关论文
共 27 条
[1]
BONDAR RJL, 1974, CLIN CHEM, V20, P586
[2]
Diagnosis, prediction, and natural course of HIV-1 protease-inhibitor-associated lipodystrophy, hyperlipidaemia, and diabetes mellitus: a cohort study [J].
Carr, A ;
Samaras, K ;
Thorisdottir, A ;
Kaufmann, GR ;
Chisholm, DJ ;
Cooper, DA .
LANCET, 1999, 353 (9170) :2093-2099
[3]
Cox D. R., 1984, Analysis of survival data
[4]
Ischemic cardiovascular disease in persons with human immunodeficiency virus infection [J].
David, MH ;
Hornung, R ;
Fichtenbaum, CJ .
CLINICAL INFECTIOUS DISEASES, 2002, 34 (01) :98-102
[5]
Report card [J].
Davidson, MB .
DIABETES CARE, 2004, 27 (01) :1-1
[6]
Dever LL, 2000, ANN PHARMACOTHER, V34, P580
[7]
Direct interference of HIV protease inhibitors with pancreatic β-cell function [J].
Düfer, M ;
Neye, Y ;
Krippeit-Drews, P ;
Drews, G .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2004, 369 (06) :583-590
[8]
Guidelines for using antiretroviral agents among HIV-infected adults and adolescents - The panel on clinical practices for treatment of HIV [J].
Dybul, M ;
Fauci, AS ;
Bartlett, JG ;
Kaplan, JE ;
Pau, AK .
ANNALS OF INTERNAL MEDICINE, 2002, 137 (05) :381-433
[9]
Genuth S, 2003, DIABETES CARE, V26, P3160
[10]
Metabolic abnormalities and cardiovascular disease risk factors in adults with human immunodeficiency virus infection and lipodystrophy [J].
Hadigan, C ;
Meigs, JB ;
Corcoran, C ;
Rietschel, P ;
Piecuch, S ;
Basgoz, N ;
Davis, B ;
Sax, P ;
Stanley, T ;
Wilson, PWF ;
D'Agostino, RB ;
Grinspoon, S .
CLINICAL INFECTIOUS DISEASES, 2001, 32 (01) :130-139