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儿童复发性艰难梭菌感染行粪便微生物移植对肾脏替代治疗的影响:一项初步研究。

Effects of fecal microbiota transplantation for recurrent Clostridium difficile infection in children on kidney replacement therapy: a pilot study.

机构信息

Department of Pediatric Nephrology and Solid Organ Transplantation, UZ Leuven, Leuven, Belgium.

Department of Microbiology and Immunology, Rega Institute for Medical Research, Leuven, Belgium.

出版信息

Pediatr Nephrol. 2024 Apr;39(4):1201-1212. doi: 10.1007/s00467-023-06168-6. Epub 2023 Sep 30.


DOI:10.1007/s00467-023-06168-6
PMID:37775582
Abstract

BACKGROUND: Recurrent Clostridium difficile infection (rCDI) is a rising problem in children with chronic diseases. Fecal microbiota transplantation (FMT) is a recent alternative for rCDI patients who do not respond to conventional treatment. FMT could have an additional positive effect on the intestinal dysbiosis and accumulation of uremic retention molecules (URM) associated with chronic kidney disease (CKD). Our aim was to investigate the clinical efficacy of FMT for rCDI in children with CKD together with the effect on dysbiosis and URM levels. METHODS: We analyzed stool and blood samples before and until 3 months after FMT in 3 children between 4 and 8 years old with CKD and rCDI. The microbiome was analyzed by 16 s rRNA sequencing. URM were analyzed with ultra-performance liquid chromatography-tandem mass spectrometry. CRP and fecal calprotectin were analyzed as parameters for systemic and gut inflammation, respectively. RESULTS: CDI resolved after FMT in all three without adverse events; one patient needed a second FMT. No significant effect on CRP and calprotectin was observed. Stool samples demonstrated a reduced richness and bacterial diversity which did not improve after FMT. We did observe a trend in the decrease of specific URM up to 3 months after FMT. CONCLUSION: FMT is an effective treatment for rCDI in patients with CKD. Analysis of the microbiome showed an important intestinal dysbiosis that, besides a significant reduction in Clostridium difficile, did not significantly change after FMT. A trend for reduction was seen in some of the measured URM after FMT.

摘要

背景:复发性艰难梭菌感染(rCDI)是患有慢性疾病的儿童中日益严重的问题。粪便微生物群移植(FMT)是 rCDI 患者对常规治疗无反应的一种新选择。FMT 可能对与慢性肾脏病(CKD)相关的肠道菌群失调和尿毒症潴留分子(URM)的积累产生额外的积极影响。我们的目的是研究 FMT 治疗儿童 CKD 合并 rCDI 的临床疗效及其对肠道菌群失调和 URM 水平的影响。

方法:我们分析了 3 名 4 至 8 岁患有 CKD 和 rCDI 的儿童在 FMT 前和 FMT 后 3 个月的粪便和血液样本。通过 16s rRNA 测序分析微生物组。采用超高效液相色谱-串联质谱法分析 URM。CRP 和粪便钙卫蛋白分别作为全身和肠道炎症的参数进行分析。

结果:所有 3 例患儿在 FMT 后 CDI 均得到缓解,无不良反应;1 例患儿需要进行第二次 FMT。CRP 和钙卫蛋白无明显变化。粪便样本显示丰富度和细菌多样性降低,FMT 后并未改善。我们观察到 FMT 后特定 URM 呈下降趋势,直至 3 个月。

结论:FMT 是 CKD 合并 rCDI 患者的有效治疗方法。对微生物组的分析显示存在严重的肠道菌群失调,除艰难梭菌大量减少外,FMT 后并未明显改变。FMT 后部分测量的 URM 呈下降趋势。

相似文献

[1]
Effects of fecal microbiota transplantation for recurrent Clostridium difficile infection in children on kidney replacement therapy: a pilot study.

Pediatr Nephrol. 2024-4

[2]
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Cochrane Database Syst Rev. 2023-4-25

[3]
Successful therapy of Clostridium difficile infection with fecal microbiota transplantation.

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[4]
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[5]
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[6]
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[7]
Identification and engraftment of new bacterial strains by shotgun metagenomic sequence analysis in patients with recurrent Clostridioides difficile infection before and after fecal microbiota transplantation and in healthy human subjects.

PLoS One. 2021

[8]
Complete Microbiota Engraftment Is Not Essential for Recovery from Recurrent Clostridium difficile Infection following Fecal Microbiota Transplantation.

mBio. 2016-12-20

[9]
Alteration of gut microbial composition associated with the therapeutic efficacy of fecal microbiota transplantation in Clostridium difficile infection.

J Formos Med Assoc. 2022-9

[10]
Microbiome changes associated with sustained eradication of Clostridium difficile after single faecal microbiota transplantation in children with and without inflammatory bowel disease.

Aliment Pharmacol Ther. 2015-7-21

引用本文的文献

[1]
A Critical Review on the Potential of Inactivated Bacteria in Counteracting Human Pathogens.

Curr Microbiol. 2025-5-20

[2]
Gut microbiota-targeted therapies in pediatric chronic kidney disease: gaps and opportunities.

Pediatr Nephrol. 2025-5-1

[3]
Sex differences in the association between long-term ambient particulate air pollution and the intestinal microbiome composition of children.

Environ Int. 2025-5

[4]
Liquid Chromatography-Mass Spectrometry Analytical Methods for the Quantitation of -Cresol Sulfate and Indoxyl Sulfate in Human Matrices: Biological Applications and Diagnostic Potentials.

Pharmaceutics. 2024-5-30

本文引用的文献

[1]
Inflammation in Children with CKD Linked to Gut Dysbiosis and Metabolite Imbalance.

J Am Soc Nephrol. 2022-12

[2]
Fecal Microbiota Transplant for Clostridioides Difficile Infection Is Safe and Efficacious in an Immunocompromised Cohort.

Dig Dis Sci. 2022-10

[3]
The Role of Microbiota in Infant Health: From Early Life to Adulthood.

Front Immunol. 2021

[4]
Fecal Calprotectin, CRP and Leucocytes in IBD Patients: Comparison of Biomarkers With Biopsy Results.

J Can Assoc Gastroenterol. 2020-3-27

[5]
Fecal Microbiota Transplantation for Treatment of Severe Clostridioides difficile Colitis in a Pediatric Patient With Non-Hodgkin Lymphoma.

J Pediatr Hematol Oncol. 2021-8-1

[6]
Gut microbiota generation of protein-bound uremic toxins and related metabolites is not altered at different stages of chronic kidney disease.

Kidney Int. 2020-6

[7]
Characterizing the gut microbiota in patients with chronic kidney disease.

Postgrad Med. 2020-4-2

[8]
Fecal microbiota transplantation in a toddler after heart transplant was a safe and effective treatment for recurrent Clostridiodes difficile infection: A case report.

Pediatr Transplant. 2020-2

[9]
Fecal microbiota transplantation for refractory diarrhea in immunocompromised diseases: a pediatric case report.

Ital J Pediatr. 2019-8-28

[10]
Alterations to the Gut Microbiota and Their Correlation With Inflammatory Factors in Chronic Kidney Disease.

Front Cell Infect Microbiol. 2019-6-12

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