Evidence map›Paper›PMID 37064012›Full record

ArticleGlomerular diseases

Patterns of Renal Dysfunction and Profile of Kidney Biopsies in Hematopoietic Stem Cell Transplant Recipients.

Elenjickal Elias John, Sanjeet Roy, Anup J Devasia, Reka Karuppusami, Nisha Jose, Selvin Sundar Raj Mani, Jeethu Joseph Eapen, Sabina Yusuf, Athul Thomas, Anna T Valson and 5 more

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Article in Glomerular diseases. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.0field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 1 institution in 1 country.

Elenjickal Elias JohnDepartment of Nephrology, Christian Medical College, Vellore, India.
Sanjeet RoyDepartment of Pathology, Christian Medical College, Vellore, India.
Anup J DevasiaDepartment of Hematology, Christian Medical College, Vellore, India.
Reka KaruppusamiDepartment of Biostatistics, Christian Medical College, Vellore, India.
Nisha JoseDepartment of Nephrology, Christian Medical College, Vellore, India.
Selvin Sundar Raj ManiDepartment of Nephrology, Christian Medical College, Vellore, India.
Jeethu Joseph EapenDepartment of Nephrology, Christian Medical College, Vellore, India.
Sabina YusufDepartment of Nephrology, Christian Medical College, Vellore, India.
Athul ThomasDepartment of Nephrology, Christian Medical College, Vellore, India.
Anna T ValsonDepartment of Nephrology, Christian Medical College, Vellore, India.
Vinoi George DavidDepartment of Nephrology, Christian Medical College, Vellore, India.
Vikram MathewsDepartment of Hematology, Christian Medical College, Vellore, India.
Biju GeorgeDepartment of Hematology, Christian Medical College, Vellore, India.
Santosh VarugheseDepartment of Nephrology, Christian Medical College, Vellore, India.
Suceena AlexanderDepartment of Nephrology, Christian Medical College, Vellore, India.
Christian Medical College, Vellore · IN

Funding

DBT-Wellcome Trust India Alliance IA/CPHS/22/1/506541Wellcome Trust
6 · The paper itself

Abstract

Introduction: Post hematopoietic stem cell transplant (HSCT), kidney can be subjected to injury by various causes. Of these, graft versus host disease (GvHD) affecting the kidney is an under-recognized entity with no clear guidelines on its diagnosis, clinicopathological manifestations, and outcomes. Material and Methods: Out of 2,930 patients who underwent HSCT at our center between 2005 and 2020, kidney biopsy was performed in 19 allogenic and 5 autologous recipients. Results: The mean age of the cohort at transplant was 33.2 ± 7 years, and 15 (62%) were males. Median time to kidney biopsy from HSCT was 14 (IQR, 9-30) months. Aplastic anemia was the most common underlying hematological disease (54.2%). All 19 allogenic recipients were classified based on clinicopathological manifestations into either thrombotic microangiopathy (TMA, 12/19 [63%]) or nephrotic syndrome (NS, 7/19 [37%]) pattern. Glomerular tuft "mesangiolysis" was the dominant pattern of injury noted in 9/12 cases of TMA pattern. There was a predominance of acute microangiopathic changes restricted primarily to the glomerular compartment. Of the 7 patients with NS pattern, membranous nephropathy was seen in 4 (57%) and minimal change disease in 3 (43%) patients. Thirty-nine percent (7/18) stained positive for C4d which was predominantly glomerular. Allogenic recipients who did not receive immunosuppression (IS) for renal disease had a lower eGFR at biopsy, a longer latency between withdrawal of GvHD prophylaxis and biopsy, and were significantly at a higher risk of kidney failure (IS: 2/11, 18.1% vs. no IS: 2/6, 33.3%, Conclusion: Renal GvHD can present with or without "associated extra-renal GvHD" after a prolonged period of withdrawal of GvHD prophylaxis, requiring careful diagnostic vigilance and consideration of IS.

Indexed as

Graft versus host diseaseHematopoietic stem cell transplantMesangiolysisNephrotic syndromeThrombotic microangiopathy

Identifiers

PMID37064012
PMCPMC10098275
OpenAlexW4324131294

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.