Chen Hon-Jhe, Yang Hao-Yu, Hsueh Kuang-Chieh, Shen Cheng-Che, Chen Ru-Yi, Yu Hsien-Chung, Wang Tzu-Lin
Department of Family Medicine, Kaohsiung Veterans General Hospital, Kaohsiung.
Department of Psychiatry, Chiayi Branch, Taichung Veterans General Hospital, Chiayi.
Medicine (Baltimore). 2018 Oct;97(42):e12835. doi: 10.1097/MD.0000000000012835.
The study aims to investigate the association between nonalcoholic fatty liver disease (NAFLD) and osteoporosis.We employed a retrospective cohort study design using the National Health Insurance Research Database in Taiwan. Our study included 2 cohorts: 4318 patients with NAFLD and 17,272 patients without NAFLD for comparison. They were matched by sex and age on the date of enrollment between January 1, 2000 and December 31, 2003. The study population in both groups was observed from the enrollment date until December 31, 2013. The incidence and the risk ratios of subsequent osteoporosis were calculated separately in both cohorts. A Cox proportional hazards model was used to assess the potential confounding variables of NAFLD on the pathogenesis of osteoporosis.The eligible study participants comprised 4318 patients in the NAFLD and 17,272 in control cohorts. The median follow-up duration was 10.7 and 10.83 years in the NAFLD and control groups, respectively. The risk of new-onset osteoporosis was higher in patients with NAFLD than in the comparison cohort. In addition, the difference of the incidence of new-onset osteoporosis remained significant among the 2 cohorts in the follow-up durations of within 1 year and more than 10 years. Patients with NAFLD were 1.35 times more likely to develop subsequent osteoporosis compared with those without NAFLD (95% confidence interval = 1.20-1.53).Our finding indicates that NAFLD might increase the risk of developing new-onset osteoporosis. For earlier detection and intervention, screening for osteoporosis in patients with the NAFLD, especially those with lower income and co-morbid with diabetes mellitus and chronic obstructive pulmonary disease, may be recommended.
本研究旨在调查非酒精性脂肪性肝病(NAFLD)与骨质疏松症之间的关联。我们采用回顾性队列研究设计,使用台湾地区的国民健康保险研究数据库。我们的研究包括2个队列:4318例NAFLD患者和17272例无NAFLD患者作为对照。在2000年1月1日至2003年12月31日入组时,根据性别和年龄对他们进行匹配。两组的研究人群从入组日期开始观察至2013年12月31日。分别计算两个队列中随后发生骨质疏松症的发病率和风险比。采用Cox比例风险模型评估NAFLD在骨质疏松症发病机制中的潜在混杂变量。符合条件的研究参与者包括NAFLD队列中的4318例患者和对照组中的17272例患者。NAFLD组和对照组的中位随访时间分别为10.7年和10.83年。NAFLD患者新发骨质疏松症的风险高于对照组。此外,在随访1年内和10年以上时,两个队列中新发骨质疏松症的发病率差异仍然显著。与无NAFLD的患者相比,NAFLD患者发生后续骨质疏松症的可能性高1.35倍(95%置信区间=1.20-1.53)。我们的研究结果表明,NAFLD可能会增加新发骨质疏松症的风险。为了早期发现和干预,建议对NAFLD患者,尤其是低收入且合并糖尿病和慢性阻塞性肺疾病的患者进行骨质疏松症筛查。