Gender and sex considerations in HIV and bone health

被引:3
|
作者
Tang, Mei J. J. [1 ]
Alexander, Adrian [1 ]
Hoy, Jennifer F. F. [1 ,2 ,3 ]
机构
[1] Alfred Hosp, Dept Infect Dis, Melbourne, Vic, Australia
[2] Monash Univ, Cent Clin Sch, Dept Infect Dis, Melbourne, Vic, Australia
[3] Alfred Hosp, Dept Infect Dis, 85 Commercial Rd, Melbourne, Vic 3004, Australia
关键词
antiretroviral therapy; bone mineral density; fracture; gender; HIV; TENOFOVIR DISOPROXIL FUMARATE; MINERAL DENSITY; EMTRICITABINE; TESTOSTERONE; DOLUTEGRAVIR; FRACTURES; TURNOVER; COHORT; MEN;
D O I
10.1097/COH.0000000000000780
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Purpose of reviewPeople with HIV (PWHIV) are at increased risk for osteoporosis and fractures, because of the effects of HIV and inflammation and antiretroviral therapy (ART) initiation as well as traditional risk factors. This review from recent literature focuses on sex differences in rates of bone disease, risk of fractures, and effects of ART.Recent findingsWomen with HIV in resource-constrained settings experience bone loss because of the additive effect of initiating TDF-containing ART during pregnancy, lactation, and menopause. Children and adolescents experience lower bone accrual during the pubertal growth years. There has been less focus on bone health in recent trials of ART containing tenofovir alafenamide and/or integrase inhibitors. Very few clinical trials or studies compare sex-specific changes in inflammation, immune activation, response to ART and bone turnover or change in BMD resulting in significant knowledge gaps.More data is needed to determine changes in prevalence of osteopenia, osteoporosis, and fractures in the era of immediate initiation of ART at high CD4 cell counts and the use of more bone-friendly ART. The long-term effects of ART and low bone mass on fractures in the ageing population of PWHIV is yet to be realized.
引用
收藏
页码:75 / 80
页数:6
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