High prevalence of severe vitamin D deficiency in combined antiretroviral therapy-naive and successfully treated Swiss HIV patients

Objectives: To evaluate the prevalence of 25-hydroxyvitamin D [25(OH) D] deficiency in HIV-positive patients, a population at risk for osteoporosis. Design: Retrospective assessment of vitamin D levels by season and initiation of combined antiretroviral therapy (cART). Methods: 25(OH) D was measured in 211 HIV-positive patients: samples were taken before initiation of cART from February to April or from August to October as well as 12 (same season) and 18 months (alternate season) after starting cART. 1,25-Dihydroxyvitamin D [1,25(OH)(2)D] was measured in a subset of 74 patients. Multivariable analyses included season, sex, age, ethnicity, BMI, intravenous drug use (IDU), renal function, time since HIV diagnosis, previous AIDS, CD4 cell count and cART, in particular nonnucleoside reverse transcriptase inhibitor (NNRTI) and tenofovir (TDF) use. Results: At baseline, median 25(OH) Dlevels were 37 (interquartile range 20-49) nmol/l in spring and 57 (39-74) nmol/l in the fall; 25(OH) D deficiency less than 30nmol/l was more prevalent in spring (42%) than in fall (14%), but remained unchanged regardless of cART exposure. In multivariable analysis, 25(OH) D levels were higher in white patients and those with a longer time since HIV diagnosis and lower in springtime measurements and in those with active IDU and NNRTI use. 1-Hydroxylation rates were significantly higher in patients with low25(OH) D. HepatitisCseropositivity, previous AIDSand higher CD4 cell counts correlated with lower 1,25(OH)(2)D levels, whereas BMI and TDF use were associated with higher levels. InTDF-treated patients, higher 1,25(OH) 2Dcorrelated with increases in serum alkaline phosphatase. Conclusion: Based on the high rate of vitamin D deficiency in HIV-positive patients, systematic screening with consideration of seasonality is warranted. The impact of NNRTIs on 25(OH) D and TDF on 1,25(OH)(2)D needs further attention. (C) 2010 Wolters Kluwer Health | Lippincott Williams & Wilkins