Evidence map›Paper›PMID 35432201›Full record

ArticleFrontiers in endocrinology2022

Progranulin and Its Receptor Predict Kidney Function Decline in Patients With Type 2 Diabetes.

Maki Murakoshi, Tomohito Gohda, Hiroko Sakuma, Terumi Shibata, Eri Adachi, Chiaki Kishida, Saki Ichikawa, Takeo Koshida, Nozomu Kamei, Yusuke Suzuki

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 18 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

10 authors at 2 institutions in 1 country.

Maki MurakoshiDepartment of Nephrology, Faculty of Medicine, Juntendo University, Tokyo, Japan.
Tomohito GohdaDepartment of Nephrology, Faculty of Medicine, Juntendo University, Tokyo, Japan.
Hiroko SakumaDepartment of Nephrology, Faculty of Medicine, Juntendo University, Tokyo, Japan.
Terumi ShibataDepartment of Nephrology, Faculty of Medicine, Juntendo University, Tokyo, Japan.
Eri AdachiDepartment of Nephrology, Faculty of Medicine, Juntendo University, Tokyo, Japan.
Chiaki KishidaDepartment of Nephrology, Faculty of Medicine, Juntendo University, Tokyo, Japan.
Saki IchikawaDepartment of Nephrology, Faculty of Medicine, Juntendo University, Tokyo, Japan.
Takeo KoshidaDepartment of Nephrology, Faculty of Medicine, Juntendo University, Tokyo, Japan.
Nozomu KameiDepartment of Endocrinology and Metabolism, Hiroshima Red Cross Hospital and Atomic-Bomb Survivors Hospital, Hiroshima, Japan.
Yusuke SuzukiDepartment of Nephrology, Faculty of Medicine, Juntendo University, Tokyo, Japan.
Juntendo University · JPHiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Progranulin (PGRN), a growth factor, is abundantly expressed in a broad range of tissues and cell types with pleiotropic functions including inflammation, neurodegeneration, and facilitating lysosome acidification. PGRN binds to TNF receptors (TNFR) and inhibits downstream inflammatory signaling pathways. TNFR is a well-known predictor of glomerular filtration rate (GFR) decline in a variety of diseases. Therefore, we measured circulating PGRN in addition to TNFR using an enzyme-linked immunosorbent assay and explored whether it predicted renal prognosis in 201 Japanese patients with type 2 diabetes. During a median follow-up of 7.6 years, 21 participants reached primary renal endpoint, which involves a decline of at least 57% in eGFR from baseline, or the onset of end-stage renal disease. Univariate Cox regression analysis revealed that classical renal measures (GFR and albuminuria), two TNF-related biomarkers (PGRN and TNFR), and BMI were associated with this outcome. Multivariate analysis demonstrated that high levels of PGRN [HR 2.50 (95%CI 2.47-2.52)] or TNFR1 [HR 5.38 (95%CI 5.26-5.50)] were associated with this outcome after adjusting for relevant covariates. The high levels of PGRN as well as TNFR1 were associated with a risk of primary renal outcome in patients with type 2 diabetes after adjusting for established risk factors.

Indexed as

Diabetes Mellitus, Type 2Receptors, Tumor Necrosis Factor, Type IFemaleHumansKidneyMaleProgranulinsReceptors, Tumor Necrosis FactorProgranulinsReceptors, Tumor Necrosis FactorReceptors, Tumor Necrosis Factor, Type Ibiomarkerdiabetic kidney diseaseprogranulin (GRN)renal outcometumor necrosis factor receptor (TNFR)

Identifiers

PMID35432201
PMCPMC9012489
OpenAlexW4221096723

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.