Saler T, Ahbab S, Sağlam Z A, Keşkek Ş Ö, Kurnaz S
Internal Medicine Department of Numune Training and Research Hospital, Adana, Turkey.
Internal Medicine Department of Haseki Training and Research Hospital, Istanbul, Turkey.
Hippokratia. 2014 Jul-Sep;18(3):240-4.
Osteoporosis is defined as the decrease in bone mineral density. It is a serious health problem showing the predisposed person with increased bone fracture risk. Hyperthyroidism is one of the major causes of secondary osteoporosis. The aim of this study was to assess bone mineral density in premenopausal women with endogenous subclinical hyperthyroidism.
A total of 168 subjects were included in this case-control study, of whom 86 and 82 participants were premenopausal women with subclinical hyperthyroidism and healthy premenopausal subjects, respectively. The patients with subclinical hyperthyroidism who were not receiving L-thyroxine treatment were included. The women in postmenopausal state or having chronic disease were excluded. The bone mineral densities of all subjects with dual energy X-ray absorptiometry were examined.
The Z scores (femur and L1-4) of the study group were -0.15 ± 1.15 and -0.23 ± 1.03, respectively. The Z scores of the control group were -0.39 ± 1.08 and -0.55 ± 0.98, respectively. The differences between the groups were not statistically significant (p=0.14, 0.34, respectively).
Our data suggest that contrary to exogenous subclinical hyperthyroidism, endogenous subclinical hyperthyroidism may not decrease bone mineral density in premenopausal women and it may not a risk factor for osteopenia or osteoporosis. Hippokratia 2014; 18 (3): 240-244.
骨质疏松症被定义为骨矿物质密度降低。它是一个严重的健康问题,使易患人群骨折风险增加。甲状腺功能亢进症是继发性骨质疏松症的主要原因之一。本研究的目的是评估内源性亚临床甲状腺功能亢进症的绝经前女性的骨矿物质密度。
本病例对照研究共纳入168名受试者,其中86名和82名参与者分别为患有亚临床甲状腺功能亢进症的绝经前女性和健康绝经前受试者。纳入未接受左甲状腺素治疗的亚临床甲状腺功能亢进症患者。排除处于绝经后状态或患有慢性病的女性。使用双能X线吸收法检查所有受试者的骨矿物质密度。
研究组的Z值(股骨和L1-4)分别为-0.15±1.15和-0.23±1.03。对照组的Z值分别为-0.39±1.08和-0.55±0.98。两组之间的差异无统计学意义(p分别为0.14和0.34)。
我们的数据表明,与外源性亚临床甲状腺功能亢进症相反,内源性亚临床甲状腺功能亢进症可能不会降低绝经前女性的骨矿物质密度,也可能不是骨质减少或骨质疏松症的危险因素。《希波克拉底》2014年;18(3):240-244。