Evidence map›Paper›PMID 39390206›Full record

ArticleScientific reports2024

Clinical relevance of proteinuria selectivity index and fractional excretion of sodium in patients with nephrotic syndrome.

Takashin Nakayama, Tatsuhiko Azegami, Shintaro Yamaguchi, Keita Hirano, Motoaki Komatsu, Kentaro Fujii, Koji Futatsugi, Hidenori Urai, Takahisa Kawaguchi, Tomoaki Itoh and 11 more

Abstract readMulticenter Study
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

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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

21 authors.

Takashin NakayamaDivision of Nephrology, Endocrinology and Metabolism, Department of Internal Medicine, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-Ku, Tokyo, 160-8582, Japan.
Tatsuhiko AzegamiDivision of Nephrology, Endocrinology and Metabolism, Department of Internal Medicine, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-Ku, Tokyo, 160-8582, Japan. t.azegami-1114@z2.keio.jp.
Shintaro YamaguchiDivision of Nephrology, Endocrinology and Metabolism, Department of Internal Medicine, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-Ku, Tokyo, 160-8582, Japan. yama1005@a6.keio.jp.
Keita HiranoDivision of Nephrology and Hypertension, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan.
Motoaki KomatsuDepartment of Nephrology, Tokyo Saiseikai Central Hospital, Tokyo, Japan.
Kentaro FujiiDepartment of Nephrology, Keiyu Hospital, Kanagawa, Japan.
Koji FutatsugiDepartment of Nephrology, Tachikawa Hospital, Tokyo, Japan.
Hidenori UraiDivision of Endocrinology, Metabolism and Nephrology, Department of Internal Medicine, Sano Kosei General Hospital, Tochigi, Japan.
Takahisa KawaguchiDepartment of Nephrology, Kawasaki Municipal Hospital, Kanagawa, Japan.
Tomoaki ItohDepartment of Nephrology, JCHO Saitama Medical Center, Saitama, Japan.
Norifumi YoshimotoDivision of Nephrology, Endocrinology and Metabolism, Department of Internal Medicine, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-Ku, Tokyo, 160-8582, Japan.
Aika HagiwaraDivision of Nephrology, Endocrinology and Metabolism, Department of Internal Medicine, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-Ku, Tokyo, 160-8582, Japan.
Akihito HishikawaDivision of Nephrology, Endocrinology and Metabolism, Department of Internal Medicine, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-Ku, Tokyo, 160-8582, Japan.
Hiroto MatsudaDepartment of Nephrology, Keiyu Hospital, Kanagawa, Japan.
Takashi AndoDepartment of Nephrology, Kawasaki Municipal Hospital, Kanagawa, Japan.
Yasuyoshi YamajiDepartment of Nephrology, JCHO Saitama Medical Center, Saitama, Japan.
Marohito MurakamiDivision of Endocrinology, Metabolism and Nephrology, Department of Internal Medicine, Sano Kosei General Hospital, Tochigi, Japan.
Akinori HashiguchiDepartment of Pathology, Keio University School of Medicine, Tokyo, Japan.
Yuko KanekoDivision of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.
Takashi YokooDivision of Nephrology and Hypertension, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan.
Kaori HayashiDivision of Nephrology, Endocrinology and Metabolism, Department of Internal Medicine, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-Ku, Tokyo, 160-8582, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proteinuria selectivity index (PSI) is a potential tool for histological classification and prediction of treatment response in nephrotic syndrome, but evidence is insufficient. Clinical relevance of fractional excretion of sodium (FENa) in nephrotic syndrome remains largely unexplored. This multicenter retrospective study included patients with nephrotic syndrome who underwent kidney biopsy between January 2012 and June 2022. Optimal cutoffs for predicting complete remission based on PSI and FENa were determined using receiver operating characteristic curves. Patients were divided into two groups using these cutoffs and followed until complete remission. Of the 611 patients included, 177 had minimal change disease (MCD), 52 had focal segmental glomerulosclerosis (FSGS), and 149 had membranous nephropathy (MN). Median (interquartile range) PSI were 0.14 (0.09-0.19) for MCD, 0.33 (0.23-0.40) for FSGS, and 0.20 (0.14-0.30) for MN. FENa were 0.24 (0.09-0.68), 1.03 (0.50-2.14), and 0.78 (0.41-1.28). Patients with low PSI and FENa had a higher incidence of complete remission. Cox regression analyses demonstrated that both parameters were associated with achieving complete remission (HR 2.73 [95% CI 1.97-3.81] and HR 1.93 [95% CI 1.46-2.55], respectively). PSI and FENa may be useful for histological classification and predicting remission in nephrotic syndrome.

Indexed as

Nephrotic SyndromeProteinuriaSodiumAdultBiopsyClinical RelevanceFemaleGlomerulonephritis, MembranousGlomerulosclerosis, Focal SegmentalHumansKidneyMaleMiddle AgedNephrosis, LipoidRemission InductionRetrospective StudiesSodiumComplete remissionFractional excretion of sodiumMinimal change diseaseNephrotic syndromeProteinuria selectivity index

Identifiers

PMID39390206
PMCPMC11467306

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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.