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High Sensitivity C-reactive Protein (hs-CRP) and Body Composition in a Cohort of HIV-infected Subject from Nutrition for Healthy Living
A Mangili1,2, A Zampini3, D Jacobson1, and Christine Wanke*1,2
1Tufts Univ, Boston, MA, US; 2New England Med Ctr, Tufts Univ Sch of Med, Boston, MA, US; and 3Friedman Sch of Nutrition Sci and Policy, Tufts Univ, Boston, MA, US
Background: Metabolic and morphologic derangements are
frequent complications of HIV disease and its treatment, and may be associated
with chronic inflammation. Some of these abnormalities, including changes in
body fat distribution, are also associated with an increased risk for
cardiovascular disease (CVD). High sensitivity C-reactive protein (hs-CRP), a
sensitive marker of inflammation, is a powerful predictor of CVD, however the
association of hs-CRP with body composition changes in HIV infection has not
been described. We examined the association of hs-CRP with body shape changes
as measured by anthropometry and dual energy x-ray absorptiometry (DEXA) in an
HIV-infected cohort.
Methods: We evaluated 422 Nutrition for Healthy Living
(NFHL) participants stratified by gender (28% female, 50% non-white). The
longitudinal association of mean hs-CRP with body composition measured 6 months
later was analyzed using generalized estimating equations (GEE) for repeated
measures controlled for race and smoking.
Results: Mean age was 43 (±7) years for women and 46
(±
7) years for men; 62% of women and 77% of men were on HAART; 64% of woman and
44% of men were current smokers. Hs-CRP was 3.47 (±4.85) in women and 3.08 (±5.3)
in men (p = 0.124). Body mass index,
triceps skinfold, fat mass by DEXA were significantly higher in women than in
men (p <0.05). In women, hs-CRP
was positively associated with limb, trunk, and whole body lean mass as
measured by DEXA (p = 0.003, 0.04,
and 0.004, respectively). In men, there was a trend for hs-CRP to positively
predict DEXA-measured trunk and whole body lean mass (p = 0.07, 0.09, respectively), but not limb lean tissue. There was
no association with fat mass in men or women. Hs-CRP positively predicted
triceps skinfold in men (p = 0.01),
but not in women. Hs-CRP was not associated with other anthropometric measures
in both genders. Adjustment for smoking and race did not significantly alter
these associations. There was no association of hs-CRP with CD4 count, HIV
viral load, glucose, or insulin.
Conclusions: Hs-CRP was associated with lean body mass as
measured by DEXA in HIV-infected women, but not in men. Hs-CRP has been shown
to be an independent predictor of mortality in HIV-infected women. Performing
hs-CRP measurements in female patients with HIV may assist in the
identification of patients in whom more aggressive assessment of metabolic,
body shape abnormalities and CVD risk might be of benefit.
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