Annapoorna N, Rao G Venkateswara, Reddy N S, Rambabu P, Rao K R S Samabasiva
Centre for Biotechnology, Acharya Nagarjuna University, Nagarjunanagar, Guntur- 522 510, A.P., India.
Int J Med Sci. 2004;1(3):152-164. doi: 10.7150/ijms.1.152. Epub 2004 Aug 5.
Osteoporosis is characterized by decreased bone mineral density and mechanistic imbalances of bone tissue that may result in reduced skeletal strength and an enhanced susceptibility to fractures. Osteoporosis in its most common form affects the elderly (both sexes) and all racial groups of human beings. Multiple environmental risk factors like acquired immune deficiency syndrome (AIDS) are believed to be one of the causes of osteoporosis. Recently a high incidence of osteoporosis has been observed in human immunodeficiency virus (HIV) infected individuals. The etiology of this occurrence in HIV infections is controversial. This problem seems to be more frequent in patients receiving potent antiretroviral therapy. In AIDS, the main suggested risk factors for the development of osteoporosis are use of protease inhibitors, longer duration of HIV infection, lower body weight before antiretroviral therapy, high viral load. Variations in serum parameters like osteocalcin, c-telopeptide, levels of elements like Calcium, Magnesium, Phosphorus, concentration of vitamin-D metabolites, lactate levels, bicarbonate concentrations, amount of alkaline phosphatase are demonstrated in the course of development of osteoporosis. OPG/RANKL/RANK system is final mediator of bone remodeling. Bone mineral density (BMD) test is of added value to assess the risk of osteoporosis in patients infected with AIDS. The biochemical markers also aid in this assessment. Clinical management mostly follows the lines of treatment of osteoporosis and osteopenia.
骨质疏松症的特征是骨矿物质密度降低和骨组织的机制失衡,这可能导致骨骼强度降低和骨折易感性增加。最常见形式的骨质疏松症影响老年人(男女皆有)以及所有种族群体。多种环境风险因素,如获得性免疫缺陷综合征(艾滋病),被认为是骨质疏松症的病因之一。最近,在感染人类免疫缺陷病毒(HIV)的个体中观察到骨质疏松症的高发病率。HIV感染中这种情况的病因存在争议。这个问题在接受强效抗逆转录病毒治疗的患者中似乎更常见。在艾滋病中,骨质疏松症发展的主要推测风险因素是蛋白酶抑制剂的使用、HIV感染持续时间较长、抗逆转录病毒治疗前体重较低、病毒载量高。在骨质疏松症发展过程中,血清参数如骨钙素、c-端肽、钙、镁、磷等元素水平、维生素D代谢物浓度、乳酸水平、碳酸氢盐浓度、碱性磷酸酶量会发生变化。OPG/RANKL/RANK系统是骨重塑的最终介质。骨矿物质密度(BMD)检测对于评估艾滋病感染患者骨质疏松症的风险具有附加价值。生化标志物也有助于这种评估。临床管理大多遵循骨质疏松症和骨质减少症的治疗方法。