Evidence map›Paper›PMID 36611910›Full record

ArticleCells2022

Glomerular Galactose-Deficient IgA1(KM55) Positive May Predict Poorer Prognosis in Coexisting Primary Membranous Nephropathy and IgA Nephropathy Patients.

Wenrong Cheng, Guoqin Wang, Weiyi Guo, Lijun Sun, Xiaoyi Xu, Hongrui Dong, Suhua Ye, Yanqiu Geng, Hong Cheng

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 78% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. Review
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

9 authors at 4 institutions in 1 country.

Wenrong ChengRenal Division, Department of Medicine, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Guoqin WangRenal Division, Department of Medicine, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Weiyi GuoRenal Division, Department of Medicine, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Lijun SunRenal Division, Department of Medicine, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Xiaoyi XuRenal Division, Department of Medicine, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Hongrui DongRenal Division, Department of Medicine, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Suhua YeDivision of Nephrology, Affiliated Hospital of Chifeng University, Neimenggu 024000, China.
Yanqiu GengDivision of Nephrology, The Third Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Hong ChengRenal Division, Department of Medicine, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Capital Medical University · CNBeijing Anzhen Hospital · CNChifeng University · CNChinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary membrane nephropathy (PMN) and IgA nephropathy (IgAN) are the most common glomerular diseases in China. Because of different pathogenesis, prognosis is significantly different. When the two diseases coexist (PMN/IgAN), the clinicopathological manifestations and prognosis remain unclear. In the present study, we analyzed the clinicopathological characteristics of PMN/IgAN patients, with only IgA deposition (PMN/IgA deposition) patients as controls. Galactose-deficient IgA1(KM55) and M-type Phospholipase A2 Receptor(PLA2R), both in circulation and renal tissues, were detected. Furthermore, prognosis of PMN/IgAN was explored. We found that PMN/IgAN also had some clinical features of IgAN in addition to PMN, such as higher serum albumin, along with a similar heavy proteinuria and lower titers of serum anti-PLA2R antibody. The positive rate of glomerular KM55 in PMN/IgAN was 23.5% (20/85), and 0% (0/29) in PMN/IgA deposition. Among those glomerular KM55 positive patients, KM55 and IgA colocalized mainly along the glomerular mesangial and capillary areas. Unfortunately, there was no significant difference in serum level of Gd-IgA1 between KM55+ and KM55- subgroups in PMN/IgAN patients, similar to the PMN/IgA deposition group. Notably, glomerular KM55 positive may predict a poorer prognosis in PMN/IgAN patients. In conclusion, our study suggested that, when glomerular KM55 staining was positive, this special coexisting PMN/IgAN disorder was prone to have more characteristics of IgAN besides PMN, and may predict poorer prognosis, while the mechanism requires further investigation.

Indexed as

Glomerulonephritis, IGAGlomerulonephritis, MembranousGalactoseHumansImmunoglobulin AGalactosegalactosyl-deficient IgA1Immunoglobulin Agalactose-deficient IgA1IgA depositionIgA nephropathyKM55primary membranous nephropathyprognosis

Identifiers

PMID36611910
PMCPMC9818871
OpenAlexW4313415027

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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.