Lin Shih-Yi, Hsu Wu-Huei, Lin Cheng-Chieh, Lin Cheng-Li, Tsai Chung-Hao, Kao Chia-Hung
Graduate Institute of Clinical Medical Science, College of Medicine, China Medical University, Taichung, Taiwan.
Division of Nephrology and Kidney Institute, China Medical University Hospital, Taichung, Taiwan.
PLoS One. 2017 Jun 12;12(6):e0179358. doi: 10.1371/journal.pone.0179358. eCollection 2017.
Chronic exocrine pancreatic insufficiency can lead to osteoporosis. However, the incidence and risk of osteoporosis after acute inflammation of pancreas remained known. Thus, we conducted a population-based cohort study to clarify the association between acute pancreatitis (AP) and osteoporosis.
Patients newly diagnosed with AP with index date between 2000 and 2011 were identified from the National Health Insurance Research Database. Osteoporosis were defined according to the International Classification of Diseases, Ninth Revision, Clinical Modification codes. We applied age-, sex-, and comorbidities-adjusted variable Cox proportional hazard models for assessing the association between AP and osteoporosis. Moreover, these models were used to adjust for the influences of patient characteristics and comorbidities.
In this study, 4,016 patients were included in the AP cohort (males, 67.9%; mean age, 51.8 years) and 4,016 matched controls in the non-AP cohort. After a mean follow-up period of 4.97 and 5.21 years in the AP and non-AP cohorts, respectively, the incidence of osteoporosis was 8.22 per 1000 person-years in the AP cohort. The AP cohort had a higher risk [adjusted hazard ratio (aHR) = 1.27, 95% confidence interval (CI) = 1.02-1.58] of osteoporosis than did the non-AP cohort. The risk of osteoporosis was highest in the female patients of the AP cohort (aHR = 2.26, 95% CI = 1.85-2.76) and patients aged 50-64 years (aHR = 4.14, 95% CI = 3.13-5.47).
AP patients are at a risk of osteoporosis, especially female gender and age 50-64 years. Those with > 3 episodes of AP had highest significant risk of developing osteoporosis.
慢性外分泌性胰腺功能不全可导致骨质疏松。然而,胰腺急性炎症后骨质疏松的发病率和风险仍不明确。因此,我们开展了一项基于人群的队列研究,以阐明急性胰腺炎(AP)与骨质疏松之间的关联。
从国民健康保险研究数据库中识别出2000年至2011年期间确诊为AP且有索引日期的患者。骨质疏松症根据国际疾病分类第九版临床修订编码进行定义。我们应用年龄、性别和合并症调整的可变Cox比例风险模型来评估AP与骨质疏松症之间的关联。此外,这些模型用于调整患者特征和合并症的影响。
本研究中,AP队列纳入了4016例患者(男性占67.9%;平均年龄51.8岁),非AP队列纳入了4016例匹配对照。AP队列和非AP队列的平均随访期分别为4.97年和5.21年,AP队列中骨质疏松症的发病率为每1000人年8.22例。与非AP队列相比,AP队列发生骨质疏松症的风险更高[调整后风险比(aHR)=1.27,95%置信区间(CI)=1.02-1.58]。AP队列中女性患者(aHR=2.26,95%CI=1.85-2.76)和50-64岁患者(aHR=4.14,95%CI=3.13-5.47)发生骨质疏松症的风险最高。
AP患者有患骨质疏松症的风险,尤其是女性和50-64岁的患者。AP发作超过3次的患者发生骨质疏松症的风险最高。