Predictors for Irreversibility of Contrast-Induced Acute Kidney Injury in Patients with Obesity After Contrast-Enhanced Computed Tomography Coronary Angiography.

IF 3.4 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Tetiana A Berezina, Oleksandr O Berezin, Michael Lichtenauer, Alexander E Berezin
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引用次数: 0

Abstract

Introduction: Although contrast-induced (CI) acute kidney injury (AKI) is a common complication in high-risk individuals requiring evaluation with contrast-enhanced angiography, the possible predictors of CI-AKI in patients with obesity are not fully understood. The aim of this study was to elucidate plausible factors associated with the irreversibility of CI-AKI in individuals with obesity undergoing contrast-enhanced computed tomography coronary angiography.

Methods: A total of 96 adult patients with obesity and the KDIGO criteria of CI-AKI (increase of serum levels of creatinine ≥ 25% or ≥ 500 µmol/L at 48 h after procedure) were retrospectively screened from the cohort of 1833 patients who underwent iodine contrast medium (ICM)-enhanced computed tomography coronary angiography, and were included in the study. The patients were divided into two cohorts: 96 adult patients with obesity and recovery of CI-AKI in 7 days after initiating of the event, and 57 individuals with irreversibility of CI-AKI. Serum concentrations of conventional biochemistry and urine biomarkers [i.e., hemoglobin, creatinine, high-sensitivity C-reactive protein, urinary albumin/creatinine ratio (UACR)] as well as natriuretic peptide, adropin, apelin, irisin, tumor necrosis factor-alpha (TNF-alpha), were determined at baseline. The levels of creatinine were measured at baseline, at the event, and in 7 days after the event.

Results: We identified 12 variables, which were associated with irreversibility of CI-AKI: age > 75 years [odds ratio (OR) = 1.22. P = 0.001], male gender (OR = 1.03, P = 0.042), stable coronary artery disease (OR = 1.06, P = 0.048), chronic kidney disease (CKD) 1-3 grade (OR = 1.60, P = 0.001), heart failure with preserved ejection fraction (HFpEF) (OR = 1.07, P = 0.046), baseline estimated GFR < 80 mL/min/1.73 m2 (OR = 1.10, P = 0.040), UACR > 17.5 mg/g Cr (OR = 1.05, P = 0.048), TNF-alpha > 3.11 pg/mL (OR = 1.12, P = 0.001), and adropin < 2.43 ng/mL (OR = 1.18, P = 0.001). After adjustment for CKD and UACR > 17.5 mg/g Cr, only HFpEF (OR = 1.06, P = 0.042) and adropin < 2.43 ng/mL (OR = 1.11, P = 0.001) remained independent predictors of CI-AKI irreversibility. Yet, adropin < 2.43 ng/mL at baseline exerted sufficiently better predictive ability than both HFpEF and preexisting CKD 1-3 grade.

Conclusion: In a multivariate prediction model adjusted for CKD and urinary albumin/creatinine ratio > 17.5 mg/g Cr, low levels of adropin (< 2.43 ng/mL) in individuals with non-morbid obesity together with the presence of HFpEF were independent predictors of CI-AKI irreversibility after ICM-enhanced computed tomography coronary angiography.

肥胖症患者进行对比度增强计算机断层扫描冠状动脉造影术后对比度诱发急性肾损伤不可逆的预测因素。
导言:虽然造影剂诱发(CI)急性肾损伤(AKI)是需要使用造影剂增强血管造影术进行评估的高危人群中常见的并发症,但肥胖症患者发生 CI-AKI 的可能预测因素尚不完全清楚。本研究旨在阐明与接受造影剂增强计算机断层扫描冠状动脉造影术的肥胖患者 CI-AKI 不可逆性相关的合理因素:从接受碘造影剂(ICM)增强型计算机断层扫描冠状动脉造影术的 1833 名患者队列中回顾性筛选出 96 名肥胖且符合 KDIGO CI-AKI 标准(术后 48 小时血清肌酐水平升高≥ 25% 或≥ 500 µmol/L)的成年患者,并将其纳入研究。这些患者被分为两组:96名肥胖且在事件发生后7天内恢复CI-AKI的成年患者和57名CI-AKI不可逆转的患者。基线时测定血清中常规生化指标和尿液生物标志物的浓度[即血红蛋白、肌酐、高敏 C 反应蛋白、尿白蛋白/肌酐比值 (UACR)],以及钠尿肽、阿托品、凋亡素、鸢尾素、肿瘤坏死因子-α (TNF-α)。在基线、事件发生时和事件发生后 7 天内测量了肌酐水平:我们确定了与 CI-AKI 不可逆性相关的 12 个变量:年龄大于 75 岁[比值比 (OR) = 1.22,P = 0.001]、男性(OR = 1.03,P = 0.042)、稳定型冠状动脉疾病(OR = 1.06,P = 0.048)、慢性肾脏病(CKD)1-3 级(OR = 1.60,P = 0.001)、射血分数保留型心衰(HFpEF)(OR = 1.07,P = 0.046)、基线估计 GFR 2(OR = 1.10,P = 0.040)、UACR > 17.5 mg/g Cr(OR = 1.05,P = 0.048)、TNF-α > 3.11 pg/mL(OR = 1.12,P = 0.001)和阿托品 17.5 mg/g Cr,只有 HFpEF(OR = 1.06,P = 0.042)和阿托品 结论:在调整了慢性肾脏病和尿白蛋白/肌酐比值 > 17.5 mg/g Cr 的多变量预测模型中,低水平的阿托品(OR = 1.06,P = 0.042
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advances in Therapy
Advances in Therapy 医学-药学
CiteScore
7.20
自引率
2.60%
发文量
353
审稿时长
6-12 weeks
期刊介绍: Advances in Therapy is an international, peer reviewed, rapid-publication (peer review in 2 weeks, published 3–4 weeks from acceptance) journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of therapeutics and interventions (including devices) across all therapeutic areas. Studies relating to diagnostics and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. The journal is of interest to a broad audience of healthcare professionals and publishes original research, reviews, communications and letters. The journal is read by a global audience and receives submissions from all over the world. Advances in Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an international and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of all scientifically and ethically sound research.
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