Department of Endocrinology, "St. Spiridon" Hospital, "Grigore T. Popa" University of Medicine and Pharmacy, No. 1 Independentei Blvd, 700111, Iasi, Romania.
Immunology Department, "St. Spiridon" Hospital, No.1 Independentei Blvd, 700111, Iasi, Romania.
J Endocrinol Invest. 2018 Aug;41(8):995-1003. doi: 10.1007/s40618-018-0826-z. Epub 2018 Jan 16.
Current fracture risk assessment options in men call for improved evaluation strategies. Recent research directed towards non-classic bone mass determinants have often yielded scarce and conflicting results. We aimed at investigating the impact of novel potential bone mass regulators together with classic determinants of bone status in healthy young and middle-aged men.
Anthropometric measurements, all-site bone mineral density (BMD) and body composition parameters assessed by dual-energy X-ray absorptiometry and also serum concentrations of (1) the adipokines leptin and resistin, (2) vitamin D and parathormone (PTH), (3) sex hormone binding globulin (SHBG), total testosterone and estradiol (free testosterone was also calculated) and (4) C-terminal telopeptide of type I collagen (CTx) were obtained from 30 apparently healthy male volunteers aged 20-65 years enrolled in this cross-sectional study.
Only lean mass (LM) and total estradiol independently predicted BMD in men in multiple regression analysis, together explaining 49% (p ≤ 0.001) of whole-body BMD variance. Hierarchical regression analysis with whole-body BMD as outcome variable demonstrated that the body mass index (BMI) beta coefficient became nonsignificant when LM was added to the model. Adipokines, fat parameters, testosterone (total and free), SHBG, PTH and vitamin D were not independently associated with BMD or CTx.
The present study shows that LM and sex hormones-namely estradiol-are the main determinants of bone mass in young and middle-aged men. The effects of BMI upon BMD seem to be largely mediated by LM. Lifestyle interventions should focus on preserving LM in men for improved bone outcomes.
目前男性骨折风险评估方法需要改进评估策略。最近针对非经典骨量决定因素的研究往往得出了稀少且相互矛盾的结果。我们旨在研究新的潜在骨量调节剂与健康年轻和中年男性骨状态的经典决定因素的共同影响。
通过双能 X 射线吸收法评估人体测量学测量、全部位骨矿物质密度 (BMD) 和身体成分参数,还测定血清中的(1)脂肪因子瘦素和抵抗素,(2)维生素 D 和甲状旁腺素 (PTH),(3)性激素结合球蛋白 (SHBG)、总睾酮和雌二醇(也计算了游离睾酮)和(4)I 型胶原 C 端肽 (CTx)。来自 30 名年龄在 20-65 岁之间的明显健康男性志愿者,他们参加了这项横断面研究。
只有瘦体重 (LM) 和总雌二醇在多元回归分析中独立预测了男性的 BMD,共同解释了全身体 BMD 方差的 49%(p≤0.001)。以全身体 BMD 为因变量的层次回归分析表明,当将 LM 添加到模型中时,体重指数 (BMI) 系数变得无统计学意义。脂肪因子、脂肪参数、睾酮(总睾酮和游离睾酮)、SHBG、PTH 和维生素 D 与 BMD 或 CTx 无独立相关性。
本研究表明,LM 和性激素(即雌二醇)是年轻和中年男性骨量的主要决定因素。BMI 对 BMD 的影响似乎主要由 LM 介导。生活方式干预应侧重于保留男性的 LM,以改善骨量结果。