Abstract

This study aimed to explore the associations between renal-related and arterial stiffness biomarkers with all-cause and expanded cardiovascular disease (CVD) mortality in a general Taiwanese population. This prospective community-based cohort study included 4883 subjects aged ≥ 20 years who were followed up until December 31, 2016. Renal-related biomarkers consisted of blood urea nitrogen (BUN), estimated glomerular filtration rate (eGFR), and urine albumin-to-creatinine ratio (UACR). Arterial stiffness biomarker consisted of brachial-ankle pulse wave velocity (baPWV). The death status of the subjects was ascertained by matching information from death records with the identification number and date of birth of the subjects. Cox proportional hazard models with restricted cubic splines estimated the hazard ratios and 95% confidence intervals for all-cause mortality and expanded CVD mortality. During a mean 8.3 years of follow up, 456 deaths were recorded, 146 of which were due to expanded CVD mortality. The multivariable-adjusted hazard ratios of all-cause mortality was 1.53 (95% CI 1.21–1.94) for BUN (≥ 20 mg/dL vs. < 20 mg/dL), 1.57 (1.15–2.14) for eGFR (< 90 mL/min/1.73 m2 vs. ≥ 90 mL/min/1.73 m2), 1.55 (1.25–1.92) for UACR (≥ 30 mg/g vs. < 30 mg/g), and 1.75 (1.14–2.67) for baPWV (≥ 1400 cm/s vs. < 1400 cm/s). The expanded CVD mortality was 1.89 (95% CI 1.30–2.73) for BUN (≥ 20 mg/dL vs. < 20 mg/dL), 2.28 (1.13–4.57) for eGFR (< 90 mL/min/1.73 m2 vs. ≥ 90 mL/min/1.73 m2), 2.13 (1.52–2.99) for UACR (≥ 25 mg/g vs. < 25 mg/g), and 15.73 (2.14–115.61) for baPWV (≥ 1400 cm/s vs. < 1400 cm/s). High levels of BUN, UACR, and baPWV and low levels of eGFR showed high risks with all-cause and expanded CVD mortality. Our study provides insights into screening tests to target populations at high risk of premature death due to CVD.

Highlights

  • Cardiovascular diseases (CVDs) are a group of disorders of the heart and blood vessels that includes coronary heart disease, stroke, and peripheral arterial disease

  • This study aimed to explore the associations between renal-related biomarkers and allcause and expanded CVD mortality among 4883 participants of Taichung Community Health Study (TCHS) and Taichung Community Health Study-Elderly (TCHS-E), as well as their family members who participated in Taichung Community Health Study-family cohort (TCHS-FC)

  • Persons who died during the follow-up period were significantly different in terms of age, gender, body mass index (BMI), educational level, marital status, smoking habits, alcohol consumption, hours spent sleeping, hours spent sitting, prevalence of heart disease, cerebrovascular disease, hypertension, diabetes, gout, cancer, waist circumference (WC), waist-to-hip ratio (WHR), waist-to-height ratio (WHtR), systolic blood pressure (SBP), diastolic blood pressure (DBP), pulse pressure (PP), mean arterial pressure (MAP), HDL-C, LDL-C, total cholesterol, fasting plasma glucose (FPG), WBC, blood urea nitrogen (BUN), estimated glomerular filtration rate (eGFR), urine albumin-to-creatinine ratio (UACR), brachial-ankle pulse wave velocity (baPWV), pulse, serum glutamic-oxalocetic transaminase (SGOT), and uric acid

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Summary

Introduction

Cardiovascular diseases (CVDs) are a group of disorders of the heart and blood vessels that includes coronary heart disease, stroke, and peripheral arterial disease. They promote the development of atherosclerotic arteries in the heart, brain, and extremities and may cause hardening and rupture of blood vessels that lead to poor blood circulation These risk factors increase the chance of causing coronary heart disease and lead to various serious complications. High levels of UACR reportedly have a positive a­ ssociation[13,14] or no association at a­ ll[15] with all-cause or CVD mortality. None of these studies that explored the association of renal-related markers with mortality considered arterial stiffness. The association was investigated by adjusting for biomarkers of metabolic syndrome and arterial stiffness

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