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老年人群中胰岛素样生长因子与骨密度关联的性别差异:兰乔贝纳多研究

Gender differences in insulin-like growth factor and bone mineral density association in old age: the Rancho Bernardo Study.

作者信息

Barrett-Connor E, Goodman-Gruen D

机构信息

Department of Family and Preventive Medicine, University of California at San Diego, La Jolla 92093-0607 USA.

出版信息

J Bone Miner Res. 1998 Aug;13(8):1343-9. doi: 10.1359/jbmr.1998.13.8.1343.

Abstract

Insulin-like growth factor-I (IGF-I) clearly plays a role in bone metabolism and maintenance, as evidenced by in vitro and animal studies. In clinical studies, the age-related decrease in IGF-I parallels the age-related decrease in bone mineral density (BMD), but several age-adjusted cross-sectional studies show no consistent association of IGF-I and BMD. We report here a cross-sectional study of serum IGF-I and BMD levels in 483 men and 455 postmenopausal women not using estrogen; subjects were 55 years of age and older, community-dwelling, ambulatory, and unselected for bone density. IGF-I was measured by a highly specific radioimmunoassay. BMD was measured at the lumbar spine and hip using dual-energy X-ray absorptiometry. Men had higher IGF-I and BMD levels than women. In age-adjusted and age-stratified models, IGF-I was associated with BMD only in women (test for interaction, p < 0.0001). Gender differences persisted in gender-specific multiple regression analyses adjusted for age, body mass index, thiazide diuretic use, current smoking, alcohol intake, physical activity, and weight change; IGF-I was significantly associated with BMD at the spine (p = 0.0001) and hip (p = 0.02) in women, but not in men (p's > 0.6). Circulating estradiol levels were not associated with IGF-I levels in either gender, testosterone was inversely associated with IGF-I and only in men. This striking gender difference has not been described previously. Its etiology is unknown. The answer could lead to improved understanding of gender differences in osteoporosis and in response to treatment with IGF-I or growth hormone.

摘要

胰岛素样生长因子-I(IGF-I)在骨代谢和维持中显然发挥着作用,体外研究和动物研究已证明这一点。在临床研究中,IGF-I随年龄的下降与骨矿物质密度(BMD)随年龄的下降相似,但几项年龄校正的横断面研究显示IGF-I与BMD之间并无一致的关联。我们在此报告一项横断面研究,该研究对483名男性和455名未使用雌激素的绝经后女性的血清IGF-I水平和BMD水平进行了检测;研究对象年龄在55岁及以上,居住在社区,能自主行走,且未因骨密度问题而被筛选。IGF-I通过高度特异性的放射免疫测定法进行测量。使用双能X线吸收法测量腰椎和髋部的BMD。男性的IGF-I和BMD水平高于女性。在年龄校正和年龄分层模型中,IGF-I仅在女性中与BMD相关(交互作用检验,p<0.0001)。在针对年龄、体重指数、噻嗪类利尿剂使用情况、当前吸烟状况、酒精摄入量、身体活动及体重变化进行校正的性别特异性多元回归分析中,性别差异依然存在;IGF-I在女性中与脊柱(p = 0.0001)和髋部(p = 0.02)的BMD显著相关,但在男性中并非如此(p>0.6)。循环雌二醇水平在两性中均与IGF-I水平无关,睾酮仅在男性中与IGF-I呈负相关。这种显著的性别差异此前尚未被描述过。其病因不明。找到答案可能有助于更好地理解骨质疏松症中的性别差异以及对IGF-I或生长激素治疗的反应。

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