Evidence map›Paper›PMID 42460295›Full record

ArticleKidney diseases (Basel, Switzerland)

Lipocalin-2 Emerges as a Core Pathogenic Mediator and Biomarker in Autosomal Dominant Tubulointerstitial Kidney Disease-UMOD via Transcriptomic Profiling.

Ruilian You, Zhi-Ying Liu, Meng-Shi Li, Yang Li, Xu-Jie Zhou, Hong Zhang

Abstract read
In one paragraph

Article in Kidney diseases (Basel, Switzerland). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Ruilian YouRenal Division, Peking University First Hospital, Beijing, China.
Zhi-Ying LiuRenal Division, Peking University First Hospital, Beijing, China.
Meng-Shi LiRenal Division, Peking University First Hospital, Beijing, China.
Yang LiRenal Division, Peking University First Hospital, Beijing, China.
Xu-Jie ZhouRenal Division, Peking University First Hospital, Beijing, China.
Hong ZhangRenal Division, Peking University First Hospital, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Autosomal dominant tubulointerstitial kidney disease (ADTKD) is a group of inherited renal disorders characterized by progressive decline in kidney function, with Methods: Transcriptomic datasets (GSE214491, GSE139585, GSE97093) from ADTKD- Results: In GSE214491 (6 mutant vs 6 wild type mice), 302 DEGs were identified at 4 months, and an additional 117 DEGs were newly characterized at 1 month, when histological disease was minimal. GSE139585 revealed 12 DEGs, and GSE97093 showed 83 and 16 DEGs in male and female cohorts, respectively. Across datasets, Lcn2 was consistently identified as a significant DEG and central hub gene and was already significantly elevated in 1-month-old ADTKD- Conclusion: LCN2 protein emerges as a reproducible biomarker and plausible pathogenic mediator across distinct

Indexed as

Autosomal dominant tubulointerstitial kidney diseaseBiomarkerLipocalin-2TranscriptomicsUMOD

Identifiers

PMID42460295
PMCPMC13372289

What OpenQuestion holds

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Registered trials

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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.