绝经后女性促甲状腺激素水平与骨质疏松性骨折的相关性研究
Correlation between thyroid stimulating hormone level and osteoporotic fracture in postmenopausal women
  
DOI:10.3969/j.issn.1006-7108.2019.06.011
中文关键词:  骨质疏松性骨折  绝经后女性  促甲状腺激素  骨密度
英文关键词:osteoporotic fracture  postmenopausal women  thyroid stimulating hormone  bone mineral density
基金项目:上海交通大学医学院附属瑞金医院“2型糖尿病危险因素的动态监测与社区综合防治”(201502007);贵州省省长资金临床应用课题专项研究[黔省专合字(2012)100号];贵州省临床重点专科培育项目
作者单位
陈庆玲 彭年春* 时立新 张巧 张淼 胡颖 贵州医科大学附属医院内分泌科贵州 贵阳 550004 
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中文摘要:
      目的 探讨绝经后女性血清促甲状腺激素水平与骨质疏松性骨折的相关性。方法 2011年5月至2011年10月期间对贵阳市云岩区4 073名40岁及以上居民开展问卷调查、体格检查、促甲状腺激素(thyroid stimulating hormone,TSH)检验及跟骨超声骨密度测定等。根据基线TSH水平,将调查对象分为3组,分别是TSH降低组(TSH<0.55 mIU/L,71人)、TSH正常组(0.55 mIU/L≤TSH≤4.78 mIU/L,3 113人)、TSH升高组(TSH>4.78 mIU/L,889人),比较各组基线特征。随访3年后,根据随访期内是否发生骨折分析不同TSH水平与骨质疏松性骨折的相关性。结果 ① TSH降低组、TSH正常组、TSH升高组中新发骨质疏松性骨折的人数分别为8例、51例、148例,发病率分别为11.3%、4.8%、5.7%,TSH降低组骨折发病率高于TSH正常组,差异具有统计学意义(P=O.O12)。TSH升高组较正常组相比差异无统计学意义。② 骨密度T值≤-2.5[OR=1.822,95% CI(1.124,2.954),P=0.004]、血脂异常[OR=1.381,95% CI(1.038,1.836),P<0.05]、TSH<0.55 mIU/L[OR=2.469,95% CI(1.163,5.243),P<0.05]是骨质疏松性骨折的危险因素,校正血脂异常、骨密度T值≤-2.5后,TSH降低组与TSH正常组相比,骨折风险增加2.626倍[OR=2.626,95% CI(1.233,5.592),P<0.05]。结论 绝经后女性TSH水平降低与骨质疏松性骨折风险增加相关。
英文摘要:
      Objective To investigate the correlation between serum thyroid stimulating hormone and osteoporotic fracture in postmenopausal women. Methods A total of4073 residents aged over 40 years old from Yunyan District, Guiyang City were investigated with questionnaire, physical examination, determination of serum TSH, and ultrasonic bone mineral density measurement of the calcaneus. According to the baseline TSH level, the subjects were divided into three groups: low (TSH<0.55 mIU/L, n=71), normal (0.55 mIU/L ≤ TSH ≤ 4.78 mIU/L, n=3113), or high (TSH>4.780 mIU/L, n=889). The baseline characteristics of each group were compared. After 3 years of follow-up, the correlation between different TSH levels and osteoporotic fractures was analyzed according to whether fractures occurred during the follow-up period. Results The number of newly developed osteoporosis fractures in the lower TSH group, the normal TSH group, and the higher TSH group were 8, 148, 51, respectively. The incidence was 11.3%, 4.8%, and 5.7%, respectively. The incidence of fracture in the lower TSH group was higher than that in normal TSH group (P<0.17). In addition, BMD T-score≤ -2.5(OR=1.822, 95%CI 1.124-2.954, P=0.004), dyslipidemia (OR=1.381, 95%CI 1.038-1.836, P=0.034), TSH<0.55 mIU/L (OR=2.469, 95%CI 1.163-5.243, P=0.019) were risk factors of osteoporotic fracture. Compared with that in the normal TSH group, the risk of fracture in the lower TSH group was increased by 2.626 times (OR=2.626, 95%CI 1.233-5.592, P=0.012) after adjusting dyslipidemia and BMD T-score≤ -2.5. Conclusion Lower TSH levels are associated with an increased risk of osteoporotic fracture in postmenopausal women.
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