National Institute for Health Research Bristol Biomedical Research Centre, University Hospitals Bristol NHS Foundation Trust and University of Bristol, Bristol, United Kingdom,
Musculoskeletal Research Unit, Translational Health Sciences, Bristol Medical School, University of Bristol, Learning and Research Building (Level 1), Southmead Hospital, Bristol, United Kingdom,
Med Princ Pract. 2019;28(5):401-409. doi: 10.1159/000499738. Epub 2019 Mar 21.
Low serum albumin concentration is associated with poor health outcomes, but its relationship with the risk of fractures has not been reliably quantified. We aimed to assess the prospective association of serum albumin with the risk of fractures in a general population.
Baseline serum albumin concentrations were measured in 2,245 men aged 42-61 years in the Kuopio Is-chemic Heart Disease study. Hazard ratios (HRs) (95% confidence intervals) were calculated for incident fractures.
A total of 121 fractures (hip, humeral, or wrist) were recorded during a median follow-up of 25.6 years. The risk of fractures increased linearly below a serum albumin concentration of ∼48 g/L. The age-adjusted HR (95% CI) for fractures per 1 standard deviation lower serum albumin was 1.24 (1.05-1.48). On further adjustment for several conventional and emerging risk factors, the HR was attenuated to 1.21 (1.01-1.45). Comparing the bottom versus top quartile of serum albumin levels, the corresponding adjusted HRs were 2.48 (1.37-4.48) and 2.26 (1.23-4.14). The association of serum albumin with fracture risk did not differ substantially according to age, body mass index, blood pressure, physical activity, alcohol consumption, socioeconomic status, inflammation, prevalent diseases, and smoking. Serum albumin at a threshold of 41.5 g/L demonstrated an area under the curve of 0.5850.
In middle-aged Caucasian men, low serum albumin is associated with an increased risk of future fractures. The potential relevance of serum albumin concentrations in fracture prevention and prediction deserves further evaluation.
血清白蛋白浓度低与健康状况不佳有关,但它与骨折风险的关系尚未得到可靠地量化。我们旨在评估一般人群中血清白蛋白与骨折风险的前瞻性关联。
在库奥皮奥缺血性心脏病研究中,对 2245 名年龄在 42-61 岁的男性进行了基线血清白蛋白浓度测量。计算了发生骨折的风险比(HR)(95%置信区间)。
在中位数为 25.6 年的随访期间,共记录了 121 例骨折(髋部、肱骨或腕部)。在血清白蛋白浓度约为 48g/L 以下,骨折风险呈线性增加。每降低 1 个标准差的血清白蛋白,年龄调整后的 HR(95%CI)为 1.24(1.05-1.48)。进一步调整几种传统和新兴的危险因素后,HR 减弱至 1.21(1.01-1.45)。比较血清白蛋白水平的最低和最高四分位数,相应的调整后 HR 分别为 2.48(1.37-4.48)和 2.26(1.23-4.14)。血清白蛋白与骨折风险的关联在年龄、体重指数、血压、体力活动、饮酒、社会经济地位、炎症、现有疾病和吸烟方面没有显著差异。血清白蛋白在 41.5g/L 的阈值下,曲线下面积为 0.5850。
在中年白种男性中,低血清白蛋白与未来骨折风险增加有关。血清白蛋白浓度在骨折预防和预测中的潜在相关性值得进一步评估。