Paper # 753 
Vitamin D and HIV-related Complications and HIV Disease Progression in Women in Tanzania
Saurabh Mehta1, D Spiegelman1, F Mugusi2, E Giovannucci1, G Msamanga2, and W Fawzi1
1Harvard Sch of Publ Hlth, Boston, MA, US and 2Muhimbili Univ of Hlth and Allied Sci, Dar es Salaam, Tanzania
Background: Vitamin D has a potential role in
preventing HIV-related complications, based on its extensive involvement in
immune function. However, this relationship has not been examined in large
studies or in resource-limited settings.
Methods: Vitamin D levels were assessed in 884
HIV-infected pregnant women at enrollment in a trial of multivitamin
supplementation (excluding vitamin D) in Tanzania. Information on HIV disease
progression and related complications was recorded during follow-up (median, 70
months). Proportional hazards models and generalized estimating equations were
used to assess the relationship of vitamin D status with these outcomes.
Results: Women with low vitamin D status (serum
25-hydroxyvitamin D <32 ng/mL) had 45% higher risk of reaching a body mass
index <18 kg/m2 during the first 2 years of follow-up, compared
to women with adequate vitamin D levels (incidence rate ratio, RR: 1.45; 95%CI
1.04 to 2.01). The relationship between continuous vitamin D levels and risk of
body mass index <18 kg/m2 during follow-up was inverse and linear
(P=0.03; Figure 1). Low vitamin D status was associated with a 25%
higher risk of progression to WHO HIV disease stage III or IV during follow-up (RR:
1.25; 1.05 to 1.50), compared to adequate vitamin D status. This risk
decreased with increasing vitamin D levels linearly (P =0.05; Figure 2).
Women with low vitamin D levels had significantly higher incidence of acute
upper respiratory infections (RR: 1.28, 1.05 to 1.55) and thrush (RR: 2.92, 1.43
to 5.96) diagnosed during the first 2 years of follow-up. Women in the lowest
vitamin D quintiles had higher incidence of mouth and throat ulcers, painful
tongue or mouth, difficult or painful swallowing, diarrhea, and fatigue during
the first 2 years of follow-up.
Conclusions: Vitamin D status has a protective
association with HIV disease progression and HIV-related complications during
follow-up in HIV-infected women. If confirmed in randomized trials, vitamin D
supplementation could represent a simple and inexpensive method to prolong the
time to ART initiation in HIV-infected patients and improve health and quality
of life, particularly in resource-limited settings.
Figure 1. Relationship of Vitamin
D Status with Wasting
(BMI <18 kg/m2) in the First 2 Years of Follow-up

Figure 2: Relationship of Vitamin
D Status with HIV Disease Progression
(Stage III/IV) during Follow-up

*Adjusted for baseline age,
CD4 T cell count, HIV disease stage and multivitamin regime
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