Longitudinal evolution of bone mineral density and bone markers in human immunodeficiency virus-infected individuals

被引:236
作者
Mondy, K
Yarasheski, K
Powderly, WG
Whyte, M
Claxton, S
DeMarco, D
Hoffmann, M
Tebas, P
机构
[1] Washington Univ, Sch Med, Dept Internal Med, Div Infect Dis, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Internal Med, Div Endocrinol, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Internal Med, Div Bone & Mineral Metab, St Louis, MO 63110 USA
关键词
D O I
10.1086/367569
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The underlying mechanisms of several bone disorders in human immunodeficiency virus (HIV)-infected persons and any relation to antiretroviral therapy have yet to be defined. A longitudinal study was conducted to estimate the prevalence of osteopenia or osteoporosis in HIV-infected persons; to assess bone mineralization, metabolism, and histomorphometry over time; and to evaluate predisposing factors. A total of 128 patients enrolled the study, and 93 were observed for 72 weeks. "Classic" risk factors (low body mass index, history of weight loss, steroid use, and smoking) for low bone mineral density (BMD) and duration of HIV infection were strongly associated with osteopenia. There was a weak association between low BMD and receipt of treatment with protease inhibitors; this association disappeared after controlling for the above factors. Markers of bone turnover tended to be elevated in the whole cohort but were not associated with low BMD. BMD increased slightly during follow-up. Traditional risk factors and advanced HIV infection play a more significant pathogenic role in the development of osteopenia and osteoporosis associated with HIV infection than do treatment-associated factors.
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页码:482 / 490
页数:9
相关论文
共 26 条
[1]  
[Anonymous], 1994, World Health Organ Tech Rep Ser, V843, P1
[2]   Impaired glucose tolerance, beta cell function and lipid metabolism in HIV patients under treatment with protease inhibitors [J].
Behrens, G ;
Dejam, A ;
Schmidt, H ;
Balks, HJ ;
Brabant, G ;
Körner, T ;
Stoll, M ;
Schmidt, RE .
AIDS, 1999, 13 (10) :F63-F70
[3]   Adverse effects of reverse transcriptase inhibitors: mitochondrial toxicity as common pathway [J].
Brinkman, K ;
ter Hofstede, HJM ;
Burger, DM ;
Smeitinkt, JAM ;
Koopmans, PP .
AIDS, 1998, 12 (14) :1735-1744
[4]   A syndrome of peripheral lipodystrophy, hyperlipidaemia and insulin resistance in patients receiving HIV protease inhibitors [J].
Carr, A ;
Samaras, K ;
Burton, S ;
Law, M ;
Freund, J ;
Chisholm, DJ ;
Cooper, DA .
AIDS, 1998, 12 (07) :F51-F58
[5]   Osteopenia in HIV-infected men: association with asymptomatic lactic acidemia and lower weight pre-antiretroviral therapy [J].
Carr, A ;
Miller, J ;
Eisman, JA ;
Cooper, DA .
AIDS, 2001, 15 (06) :703-709
[6]   Zidovudine-induced mitochondrial disorder with massive liver steatosis, myopathy, lactic acidosis, and mitochondrial DNA depletion [J].
Chariot, P ;
Drogou, I ;
de Lacroix-Szmania, I ;
Eliezer-Vanerot, MC ;
Chazaud, B ;
Lombès, A ;
Schaeffer, A ;
Zafrani, ES .
JOURNAL OF HEPATOLOGY, 1999, 30 (01) :156-160
[7]  
DUSSO A, 2000, ANTIVIR THER S, V5, P19
[8]   Myocardial infarction in HIV-infected men receiving protease inhibitors [J].
Flynn, TE ;
Bricker, LE .
ANNALS OF INTERNAL MEDICINE, 1999, 131 (07) :548-548
[9]   Fasting hyperinsulinemia and changes in regional body composition in human immunodeficiency virus-infected women [J].
Hadigan, C ;
Miller, K ;
Corcoran, C ;
Anderson, E ;
Basgoz, N ;
Grinspoon, S .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (06) :1932-1937
[10]   A controlled trial of two nucleoside analogues plus indinavir in persons with human immunodeficiency virus infection and CD4 cell counts of 200 per cubic millimeter or less [J].
Hammer, SM ;
Squires, KE ;
Hughes, MD ;
Grimes, JM ;
Demeter, LM ;
Currier, JS ;
Eron, JJ ;
Feinberg, JE ;
Balfour, HH ;
Dayton, LR ;
Chodakewitz, JA ;
Fischl, MA .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (11) :725-733