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Mapping intersectional inequalities in biomarkers of healthy ageing and chronic disease in older English adults

机译:在旧英语成人中映射健康衰老和慢性病的生物标志物中的交叉不等式

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Chronic diseases and their inequalities amongst older adults are a significant public health challenge. Prevention and treatment of chronic diseases will benefit from insight into which population groups show greatest risk. Biomarkers are indicators of the biological mechanisms underlying health and disease. We analysed disparities in a common set of biomarkers at the population level using English national data (n?=?16,437). Blood-based biomarkers were HbA1c, total cholesterol and C-reactive protein. Non-blood biomarkers were systolic blood pressure, resting heart rate and body mass index. We employed an intersectionality perspective which is concerned with how socioeconomic, gender and ethnic disparities combine to lead to varied health outcomes. We find granular intersectional disparities, which vary by biomarker, with total cholesterol and HbA1c showing the greatest intersectional variation. These disparities were additive rather than multiplicative. Each intersectional subgroup has its own profile of biomarkers. Whilst the majority of variation in biomarkers is at the individual rather than intersectional level (i.e. intersections exhibit high heterogeneity), the average differences are potentially associated with important clinical outcomes. An intersectional perspective helps to shed light on how socio-demographic factors combine to result in differential risk for disease or potential for healthy ageing.
机译:年龄较大的成年人之间的慢性疾病及其不平等是一个重要的公共卫生挑战。预防和治疗慢性病将受益于人口群体表现出最大风险的洞察力。生物标志物是潜在健康和疾病的生物机制的指标。我们使用英语国家数据分析了人口水平的常见生物标志物中的差异(n?=?16,437)。基于血液的生物标志物是HBA1C,总胆固醇和C反应蛋白。非血液生物标志物是收缩压,休息心率和体重指数。我们雇用了一个交叉的角度,涉及社会经济,性别和种族差异如何结合导致不同的健康结果。我们发现粒状交叉差异,其由生物标志物变化,总胆固醇和HBA1c显示最大的交叉变化。这些差异是添加剂而不是乘法。每个交叉子组都有自己的生物标志物的概况。虽然生物标志物的大部分变化位于个体而不是交叉水平(即交叉点表现出高异质性),但平均差异可能与重要的临床结果相关。交叉观点有助于阐明社会人口因子如何结合如何导致疾病或健康老化潜力的差异风险。

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