同种异体造血干细胞移植后肾损伤患者微生物组的变化。

IF 3.2 Q1 UROLOGY & NEPHROLOGY
Kidney360 Pub Date : 2024-10-24 DOI:10.34067/KID.0000000627
Matthew H Abramson, Insara Jaffer Sathick, Andrea Knezevic, Miguel-Angel Perales, Edgar A Jaimes
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引用次数: 0

摘要

背景:急性肾损伤(AKI)是异基因造血细胞移植(allo-HCT)的常见并发症,会增加死亡风险。与此相反,中性粒细胞移植时肠道微生物群的多样性越高,死亡率越低。我们的目的是更好地了解肾脏结果与这一患者群体肠道多样性变化的关系,假设基线和移植时微生物群多样性较低的患者发生肾脏并发症的风险较高:我们对本机构 2014-2017 年的 419 名造血细胞移植受者进行了单中心回顾性研究,并对其肠道微生物群进行了分析。我们根据 KDIGO 标准定义了 AKI 和 CKD,并使用 CKD 流行病学协作方程估算了肾小球滤过率(GFR)。我们使用香农和辛普森倒数多样性指数来定义肠道微生物组的多样性,指数越高表示微生物组越多样化:基线时,我们队列中的辛普森倒数DI和香农DI分别为21.8(IQR:13.7,35.2;范围:1.6,102.5)和3.7(IQR:3.2,4.2;范围:0.7,5.2),围移植期分别为6.3(IQR:3.7,10.4)和2.3(IQR:1.7,2.8)。在这419名患者中,263名(63%)患者在移植后100天内出现任何程度的AKI,114名(27%)患者出现2级以上AKI。与未出现肾脏并发症的患者相比,移植后出现AKI或CKD的患者在基线或移植前后的微生物组多样性没有明显差异:我们的研究结果不支持基线或移植周肠道多样性与接受异体器官移植的患者发生 AKI 或 CKD 的风险之间存在联系。这项研究强调了异体肾移植受者发生 AKI 的病因复杂且多因素,因此需要进行更多的前瞻性机理研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Changes in Microbiome in Patients with Kidney Injury after Allogeneic Hematopoietic Stem Cell Transplantation.

Background: Acute kidney injury (AKI) is a common complication of allogeneic hematopoietic cell transplantation (allo-HCT) that increases the risk of mortality. In contrast, higher diversity of intestinal microbiota at the time of neutrophil engraftment has been associated with lower mortality. We aimed to better understand kidney outcomes in relation to changes in gut diversity in this patient population, hypothesizing that patients with lower microbiome diversity at baseline and at engraftment were at higher risk of developing kidney complications.

Methods: We performed a single-center retrospective study of 419 hematopoietic cell transplant recipients from 2014-2017 at our institution whose gut microbiota were analyzed. We defined AKI and CKD based on KDIGO criteria and estimated glomerular filtration rate (GFR) using the CKD Epidemiology Collaboration equation. We defined gut microbiome diversity using Shannon and Simpson reciprocal diversity indices, with higher levels indicating more diverse microbiota.

Results: Simpson reciprocal DI and Shannon DI were 21.8 (IQR: 13.7, 35.2; range: 1.6, 102.5) and 3.7 (IQR: 3.2, 4.2; range: 0.7,5.2) in our cohort at baseline and 6.3 (IQR: 3.7, 10.4) and 2.3 (IQR: 1.7, 2.8) at peri-engraftment. Of the 419, 263 patients (63%) developed any grade AKI in 100 days post-HCT, and 114 (27%) developed Grade 2+ AKI. There were no significant differences in microbiome diversity at baseline or peri-engraftment in patients who developed post-transplant AKI or CKD, respectively, in comparison to those who did not develop kidney complications.

Conclusions: Our findings do not support the existence of a link between baseline or peri-engraftment gut diversity and the risk for development of AKI or CKD in patients undergoing allo-HCT. This study highlights the complex and multifactorial etiology of AKI in allo-HCT recipients and the need for additional prospective and mechanistic studies.

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来源期刊
Kidney360
Kidney360 UROLOGY & NEPHROLOGY-
CiteScore
3.90
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