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Clinical lipoatrophy in HIV-1 patients on HAART is not associated with increased abdominal girth, hyperlipidaemia or glucose intolerance
D Worm, 1 O Kirk, 2 O Andersen, 2 J Vinten, 1 J Gerstoft, 3 TL Katzenstein, 3 H Nielsen 4 and C Pedersen 5
  1 Department of Medical Physiology, The Panum Institute, University of Copenhagen, Copenhagen,   2 Department of Infectious Diseases, Hvidovre Hospital, University of Copenhagen, Hvidovre,   3 Department of Infectious Diseases, Rigshospitalet, University of Copenhagen, Copenhagen,   4 Department of Infectious Diseases, Aalborg Hospital, Aalborg, and   5 Department of Infectious Diseases, Odense University Hospital, Odense, Denmark
Correspondence: Dorte Worm, Department of Medical Physiology, Building 12, 6th floor, The Panum Institute, University of Copenhagen, Blegdamsvej 3, DK-2200 Copenhagen N, Denmark. e-mail: dworm@mfi.ku.dk
Copyright British HIV Association
KEYWORDS
HIV • lipoatrophy • nucleoside reverse transcriptase inhibitor • protease inhibitor

ABSTRACT

 
Objective

To compare information on body fat changes from questionnaire and clinical examination and to study lipoatrophy in HIV-1 patients on highly active antiretroviral therapy (HAART).

 
Methods

The study was cross-sectional within a randomized trial. One hundred and sixty-eight male HIV-1 patients were examined by questionnaire and clinical examination. Clinical lipoatrophy was studied and defined as fat wasting in the face, legs and/or arms. Fasting blood samples reflecting lipid and glucose metabolism were taken and the role of indinavir, ritonavir (RTV) and RTV/saquinavir (SQV) on lipoatrophy was investigated.

 
Results

After a median of 17 months on HAART, concordance rates between information on changes in body fat from questionnaire and clinical examination were significant and varied from 70 to 96%. With a positive criteria of lipoatrophy in both assessments, 14% of patients had lipoatrophy. These patients had lower weight (P = 0.0007), weight loss from baseline (P = 0.003), lower circumferences at all measurements (P < 0.01), lower plasma triglycerides and low-density lipoprotein (LDL) (P < 0.05) and longer treatment with stavudine (P = 0.0009). Homeostasis model assessment (HOMA) estimates for insulin resistance and β-cell function were comparable. Plasma cholesterol, triglycerides and very low-density lipoprotein (VLDL) were higher in patients receiving RTV or RTV/SQV (P < 0.03).

 
Conclusion

Questionnaire and clinical assessment provide concordant information on changes in body fat. Lipoatrophic patients on HAART with neither increase in abdominal circumference, nor hyperlipidaemia nor glucose intolerance may have side-effects to protease inhibitor treatment, to nucleoside reverse transcriptase inhibitor treatment (stavudine) or suffer from a drug-independent condition.


Received: 29 January 2002, accepted 9 July 2002

DIGITAL OBJECT IDENTIFIER (DOI)
10.1046/j.1468-1293.2002.00125.x About DOI

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