Impairment of Cardiovascular Functional Capacity in Mild to Moderate Kidney Dysfunction.

IF 8.5 1区 医学 Q1 UROLOGY & NEPHROLOGY
Kenneth Lim,Matthew Nayor,Eliott Arroyo,Heather N Burney,Xiaochun Li,Yang Li,Ravi Shah,Joseph Campain,Douglas Wan,Stephen Ting,Thomas F Hiemstra,Ravi Thadhani,Sharon Moe,Daniel Zehnder,Martin G Larson,Ramachandran S Vasan,Gregory D Lewis
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引用次数: 0

Abstract

BACKGROUND Traditional diagnostic tools that assess resting cardiac function and structure fail to accurately reflect cardiovascular alterations in patients with chronic kidney disease (CKD). This study sought to determine whether multidimensional exercise response patterns related to cardiovascular functional capacity can detect abnormalities in mild-to-moderate CKD. METHODS In a cross-sectional study, we examined 3,075 participants from the Framingham Heart Study (FHS) and 451 participants from the Massachusetts General Hospital Exercise Study (MGH-ExS) who underwent cardiopulmonary exercise testing (CPET). Participants were stratified by estimated glomerular filtration rate (eGFR): eGFR ≥90; eGFR 60-89; eGFR 30-59. Our primary outcomes of interest were peak oxygen uptake (VO2Peak),VO2 at anaerobic threshold (VO2AT), and the ratio of minute ventilation to carbon dioxide production (VE/VCO2). Multiple linear regression models were fitted to evaluate the associations between eGFR group and each outcome variable adjusted for covariates. RESULTS In the FHS cohort, N=1,712 (56%) had an eGFR ≥90 ml/min/1.73m2, N=1,271 (41%) had an eGFR 60-89 ml/min/1.73m2, and N=92 (3%) had an eGFR 30-59 ml/min/1.73m2. In the MGH-ExS cohort, N=247 (55%) had an eGFR ≥90 ml/min/1.73m2, N=154 (34%) had an eGFR 60-89 ml/min/1.73m2, and N=50 (11%) had an eGFR 30-59 ml/min/1.73m2. In FHS, VO2Peak and VO2AT were incrementally impaired with declining kidney function (p<0.001); however this pattern was attenuated following adjustment for age. Percent-predicted VO2Peak at AT was higher in the lower eGFR groups (p<0.001). In MGH-ExS, VO2Peak and VO2AT were incrementally impaired with declining kidney function in unadjusted and adjusted models (p<0.05). VO2Peak was associated with eGFR (p<0.05) in all models even after adjusting for age. On further mechanistic analysis, we directly measured cardiac output (CO) at peak exercise via right heart catheterization and found impaired CO in the lower eGFR groups (p≤0.007). CONCLUSION CPET-derived indices may detect impairment in cardiovascular functional capacity and track cardiac output declines in mild to moderate CKD.
轻度至中度肾功能不全对心血管功能的影响。
背景评估静息心脏功能和结构的传统诊断工具无法准确反映慢性肾脏病(CKD)患者的心血管变化。本研究试图确定与心血管功能能力相关的多维运动反应模式是否能检测出轻度至中度 CKD 患者的异常。方法在一项横断面研究中,我们对弗雷明汉心脏研究 (FHS) 的 3075 名参与者和麻省总医院运动研究 (MGH-ExS) 的 451 名参与者进行了心肺运动测试 (CPET)。参与者按估计肾小球滤过率(eGFR)分层:eGFR ≥90;eGFR 60-89;eGFR 30-59。我们关注的主要结果是峰值摄氧量(VO2Peak)、无氧阈值摄氧量(VO2AT)和分钟通气量与二氧化碳产生量之比(VE/VCO2)。结果 在 FHS 队列中,1712 人(56%)的 eGFR ≥90 ml/min/1.73m2,1271 人(41%)的 eGFR 为 60-89 ml/min/1.73m2,92 人(3%)的 eGFR 为 30-59 ml/min/1.73m2。在 MGH-ExS 队列中,247 人(55%)的 eGFR ≥90 毫升/分钟/1.73 平方米,154 人(34%)的 eGFR 为 60-89 毫升/分钟/1.73 平方米,50 人(11%)的 eGFR 为 30-59 毫升/分钟/1.73 平方米。在 FHS 中,随着肾功能的下降,VO2Peak 和 VO2AT 会逐渐减弱(p<0.001);但在对年龄进行调整后,这种模式会减弱。肾小球滤过率较低组的预测峰值 VO2 百分比更高(p<0.001)。在 MGH-ExS 中,在未调整和调整模型中,随着肾功能的下降,VO2Peak 和 VO2AT 逐渐减弱(p<0.05)。在所有模型中,即使对年龄进行调整后,VO2Peak 仍与 eGFR 相关(p<0.05)。在进一步的机理分析中,我们通过右心导管直接测量了运动峰值时的心输出量(CO),发现在 eGFR 较低的组别中,心输出量受损(p≤0.007)。
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来源期刊
CiteScore
12.20
自引率
3.10%
发文量
514
审稿时长
3-6 weeks
期刊介绍: The Clinical Journal of the American Society of Nephrology strives to establish itself as the foremost authority in communicating and influencing advances in clinical nephrology by (1) swiftly and effectively disseminating pivotal developments in clinical and translational research in nephrology, encompassing innovations in research methods and care delivery; (2) providing context for these advances in relation to future research directions and patient care; and (3) becoming a key voice on issues with potential implications for the clinical practice of nephrology, particularly within the United States. Original manuscript topics cover a range of areas, including Acid/Base and Electrolyte Disorders, Acute Kidney Injury and ICU Nephrology, Chronic Kidney Disease, Clinical Nephrology, Cystic Kidney Disease, Diabetes and the Kidney, Genetics, Geriatric and Palliative Nephrology, Glomerular and Tubulointerstitial Diseases, Hypertension, Maintenance Dialysis, Mineral Metabolism, Nephrolithiasis, and Transplantation.
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