Coronary microvascular dysfunction is associated with degree of anaemia in end‐stage renal disease

BMC Cardiovascular Disorders

Luke C. Pickup¹  Richard P. Steeds¹  Anna M. Price¹  Jonathan P. Law¹  Charles J. Ferro¹  Jonathan N. Townend¹  Ashwin Radhakrishnan¹  Roxy Senior²  Larissa Fabritz³  Kirsty C. McGee⁴ 

[1] Birmingham Cardio-Renal Group, Institute of Cardiovascular Sciences, University of Birmingham;Cardiac Research Unit, Northwick Park Hospital;Department of Cardiology, Queen Elizabeth Hospital;Institute of Inflammation and Ageing, University of Birmingham;

关键词: Coronary flow velocity reserve;    Anaemia;    End-stage renal disease;    Coronary microvascular dysfunction;   

DOI  :  10.1186/s12872-021-02025-2

来源: DOAJ

【 摘 要 】

Abstract Background Coronary microvascular dysfunction (CMD) is common in end-stage renal disease (ESRD) and is an adverse prognostic marker. Coronary flow velocity reserve (CFVR) is a measure of coronary microvascular function and can be assessed using Doppler echocardiography. Reduced CFVR in ESRD has been attributed to factors such as diabetes, hypertension and left ventricular hypertrophy. The contributory role of other mediators important in the development of cardiovascular disease in ESRD has not been studied. The aim of this study was to examine the prevalence of CMD in a cohort of kidney transplant candidates and to look for associations of CMD with markers of anaemia, bone mineral metabolism and chronic inflammation. Methods Twenty-two kidney transplant candidates with ESRD were studied with myocardial contrast echocardiography, Doppler CFVR assessment and serum multiplex immunoassay analysis. Individuals with diabetes, uncontrolled hypertension or ischaemic heart disease were excluded. Results 7/22 subjects had CMD (defined as CFVR < 2). Demographic, laboratory and echocardiographic parameters and serum biomarkers were similar between subjects with and without CMD. Subjects with CMD had significantly lower haemoglobin than subjects without CMD (102 g/L ± 12 vs. 117 g/L ± 11, p = 0.008). There was a positive correlation between haemoglobin and CFVR (r = 0.7, p = 0.001). Similar results were seen for haematocrit. In regression analyses, haemoglobin was an independent predictor of CFVR (β = 0.041 95% confidence interval 0.012–0.071, p = 0.009) and of CFVR < 2 (odds ratio 0.85 95% confidence interval 0.74–0.98, p = 0.022). Conclusions Among kidney transplant candidates with ESRD, there is a high prevalence of CMD, despite the absence of traditional risk factors. Anaemia may be a potential driver of microvascular dysfunction in this population and requires further investigation.

【 授权许可】

Unknown