Risk factors for vitamin D deficiency and relationship with cardiac biomarkers, inflammation and immune restoration in HIV-infected youth

被引:27
作者
Eckard, Allison Ross [1 ,2 ]
Judd, Suzanne E. [3 ]
Ziegler, Thomas R. [1 ]
Camacho-Gonzalez, Andres F. [1 ,2 ]
Fitzpatrick, Anne M. [1 ,2 ]
Hadley, Graham R. [1 ]
Grossmann, Ruth E. [1 ]
Seaton, LaTeshia [2 ]
Seydafkan, Shabnam [1 ]
Mulligan, Mark J. [1 ]
Rimann, Nayoka [1 ]
Tangpricha, Vin [1 ]
McComsey, Grace A. [4 ,5 ]
机构
[1] Emory Univ, Sch Med, Atlanta, GA 30322 USA
[2] Childrens Healthcare Atlanta, Atlanta, GA USA
[3] Univ Alabama Birmingham, Birmingham, AL USA
[4] Case Western Reserve Univ, Cleveland, OH 44106 USA
[5] Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA
关键词
INTIMA-MEDIA THICKNESS; CORONARY-HEART-DISEASE; 3RD NATIONAL-HEALTH; ANTIRETROVIRAL THERAPY; 25-HYDROXYVITAMIN D; BLOOD-PRESSURE; YOUNG-ADULTS; SUPPLEMENTATION; CHILDREN; ASSOCIATION;
D O I
10.3851/IMP2318
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Vitamin D deficiency is common in HIV-infected individuals. In adults, traditional and HIV-related factors play a role in vitamin D status, and deficiency appears to impair immune restoration and exacerbate HIV complications, like cardiovascular disease (CVD). This study sought to determine factors contributing to vitamin D status in HIV-infected youth and investigate the relationship with CVD risk, inflammation and immune restoration. Methods: HIV-infected subjects (1-25 years old) were enrolled prospectively along with healthy controls that were group-matched by age, sex and race. HIV data were collected for the HIV-infected group, while traditional risk factors, including vitamin D intake, sun exposure, skin pigmentation, physical activity level and body mass index (BMI) were collected for both groups. Fasting lipids, plasma 25-hydroxyvitamin D (25[OH]D), and inflammation markers were measured. Results: In total, 200 HIV-infected subjects and 50 controls were enrolled. HIV group had 53% male, 95% Black and a mean age of 17.2 +/- 4.6 years. There was no difference in 25(OH)D between groups; 77% of HIV+ and 74% of controls had 25(OH)D< 20 ng/ml. Only Fitzpatrick skin type was independently associated with 25(OH) D. No HIV variables were associated with 25(OH)D, even when HIV subpopulations were examined. Inflammation, CVD risk factors and immune restoration were not independently associated with 25(OH)D. Conclusions: Vitamin D deficiency is common among HIV-infected youth. However, HIV factors, CVD risk, inflammation and immune restoration do not appear to have the same relationship with vitamin D as has been shown in adults. Supplementation trials are needed to determine if increasing 25(OH)D concentrations could better elucidate these relationships.
引用
收藏
页码:1069 / 1078
页数:10
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