原发性醛固酮增多症是椎体骨折的危险因素

M. Notsu, M. Yamauchi, Masahiro Yamamoto, Kiyoko Nawata, T. Sugimoto
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引用次数: 30

摘要

一些观察性研究揭示了醛固酮水平过高与骨密度(BMD)降低之间的关联。然而,原发性醛固酮增多症(PA)患者是否比健康人有更高的骨折风险尚不清楚。目的本研究旨在阐明PA是否为椎体骨折(VF)的危险因素。设计和患者:我们招募了56名PA患者和56名年龄和性别匹配的健康个体。对两组患者的血清和尿液生物学参数、骨密度和室性虚通畅进行评估。我们比较了PA和对照参与者的参数,并在调整变量后进行了多元逻辑回归分析。结果PA患者的收缩压、舒张压、糖化血红蛋白(HbA1c)和甘油三酯均高于对照组,尿钙/肌酐比高于对照组,高密度脂蛋白胆固醇低于对照组(P < 0.05)。PA组VFs患病率(44.6%)明显高于对照组(23.2%),P < 0.05。PA患者出现严重骨折的频率高于对照组。对年龄、性别和体重指数进行校正后的多变量logistic回归分析发现,PA与VFs的存在相关(优势比,3.13;95%置信区间为1.30 ~ 7.51;P < 0.05)。在进一步调整收缩压和舒张压、HbA1c、甘油三酯和高密度脂蛋白胆固醇后,这种关联仍然具有统计学意义,但在调整钙-肌酐比和骨密度后,这种关联没有统计学意义。结论:我们确定PA是VF的危险因素,独立于血压、HbA1c和血脂。PA患者的骨折严重程度明显高于年龄和性别匹配的对照组。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary Aldosteronism as a Risk Factor for Vertebral Fracture
Context Some observational studies have revealed an association between excessive aldosterone levels and reduced bone mineral density (BMD). However, whether patients with primary aldosteronism (PA) are at higher risk of fracture than healthy individuals remains unclear. Objective This study aimed to clarify whether PA represents a risk factor for vertebral fracture (VF). Design and Patients We enrolled 56 patients with PA and 56 age- and sex-matched healthy individuals. Serum and urinary biological parameters, BMD, and presence of VFs were evaluated in both groups. We compared parameters between PA and control participants and performed multiple logistic regression analyses after adjustments for variables. Results Patients with PA showed higher systolic and diastolic blood pressure, higher hemoglobin A1c (HbA1c) and triglycerides, higher urinary calcium-to-creatinine ratio, and lower high-density lipoprotein cholesterol than controls (P < 0.05, each). Prevalence of VFs was significantly higher in patients with PA (44.6%) than in controls (23.2%, P < 0.05). Patients with PA showed severe fracture more frequently than controls. Multivariate logistic regression analyses adjusted for age, sex, and body mass index identified PA as being associated with the presence of VFs (odds ratio, 3.13; 95% confidence interval, 1.30 to 7.51; P < 0.05). This association remained statistically significant after further adjustment for systolic and diastolic blood pressure, HbA1c, triglycerides, and high-density lipoprotein cholesterol but not after adjustment for calcium-to-creatinine ratio and BMD. Conclusions We identified PA as a risk factor for VF, independent of blood pressure, HbA1c, and lipid profile. Fracture severity was significantly higher in patients with PA than in age- and sex-matched controls.
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