Evidence map›Paper›PMID 39867081›Full record

ArticleCureus2024

The Outcomes of IgA Nephropathy With Nephrotic Syndrome: A Clinicopathological Study From Northern India.

Abdullah, Durgesh Pushkar, Anupma Kaul, Manas R Behera, Mudit Khurana, Narayan Prasad, Dharmendra S Bhadauria, Manas R Patel, Monika Yachha, Ravi S Kushwaha

Abstract read
In one paragraph

Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

10 authors.

AbdullahNephrology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, IND.
Durgesh PushkarNephrology, King George's Medical University, Lucknow, IND.
Anupma KaulNephrology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, IND.
Manas R BeheraNephrology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, IND.
Mudit KhuranaNephrology, Sarojini Naidu Medical College, Agra, IND.
Narayan PrasadNephrology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, IND.
Dharmendra S BhadauriaNephrology, Medanta Super Speciality Hospital, Lucknow, IND.
Manas R PatelNephrology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, IND.
Monika YachhaNephrology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, IND.
Ravi S KushwahaNephrology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction Nephrotic syndrome, an unusual clinical presentation of IgA nephropathy (IgAN), occurs only in a few cases. The data regarding its clinical characteristics and treatment outcomes are lacking. Material and methods In this retrospective analysis, we reviewed kidney biopsies conducted between January 2007 and December 2018. All patients with biopsy-proven IgAN and clinical presentation of nephrotic syndrome were included. Results Sixty-seven (11.9%) out of 560 patients with primary IgAN had nephrotic syndrome as the first clinical presentation. On MEST-C scoring, the baseline estimated glomerular filtration rate (eGFR) was significantly lower in the presence of segmental sclerosis (S1) (p=0.04) and >25% tubular atrophy/interstitial fibrosis (T1/2) (p=0.004). With immunosuppression, complete remission (CR), partial remission (PR), and no response (NR) occurred in 28 (41.8%), 32 (47.8%), and 7 (10.4%) patients, respectively. During the median follow-up of 190 weeks, the median absolute change in eGFR was significant between CR and NR groups (p=0.002), and PR and NR groups (p=0.02); however, it was not significant between CR and PR groups (p=0.14). In the CR, PR, and NR groups, 9, 15, and 7 patients had eGFR losses of ≥15 ml/min (p=0.004). No patient in the CR group, one in the PR group, and three in the NR group progressed to end-stage kidney disease (ESKD) (p=0.003). Further, none of the MEST-C scores correlated with the clinical outcome parameters. Conclusion Immunosuppression in treating IgAN accompanied by nephrotic syndrome helps in proteinuria remission. Achieving remission, whether complete or partial, delays disease progression and improves renal survival. Moreover, the baseline eGFR was significantly lower when S1 and T1/2 lesions were present in kidney biopsies.

Indexed as

egfr creatinineiga nephropathy (igan)immunosuppression therapymest-c scorenephrotic syndrome

Identifiers

PMID39867081
PMCPMC11761544

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