Evidence map›Paper›PMID 38481996›Full record

ArticleFrontiers in immunology2024

Serum high mobility group box 1 as a potential biomarker for the progression of kidney disease in patients with type 2 diabetes.

Tongtong Liu, Hailing Zhao, Ying Wang, Peng Qu, Yanmei Wang, Xiai Wu, Tingting Zhao, Liping Yang, Huimin Mao, Liang Peng and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 8% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Article
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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

12 authors at 4 institutions in 1 country.

Tongtong LiuGuang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Hailing ZhaoChina-Japan Friendship Hospital, Institute of Medical Science, Beijing, China.
Ying WangDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Peng QuChina-Japan Friendship Hospital, Institute of Medical Science, Beijing, China.
Yanmei WangChina-Japan Friendship Hospital, Institute of Medical Science, Beijing, China.
Xiai WuChina-Japan Friendship Hospital, Institute of Medical Science, Beijing, China.
Tingting ZhaoChina-Japan Friendship Hospital, Institute of Medical Science, Beijing, China.
Liping YangGuang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Huimin MaoGuang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Liang PengChina-Japan Friendship Hospital, Institute of Medical Science, Beijing, China.
Yongli ZhanGuang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Ping LiChina-Japan Friendship Hospital, Institute of Medical Science, Beijing, China.
China-Japan Friendship Hospital · CNGuang’anmen Hospital · CNDongzhimen Hospital Affiliated to Beijing University of Chinese Medicine · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: As a damage-associated molecular pattern protein, high mobility group box 1 (HMGB1) is associated with kidney and systemic inflammation. The predictive and therapeutic value of HMGB1 as a biomarker has been confirmed in various diseases. However, its value in diabetic kidney disease (DKD) remains unclear. Therefore, this study aimed to investigate the correlation between serum and urine HMGB1 levels and DKD progression. Methods: We recruited 196 patients with type 2 diabetes mellitus (T2DM), including 109 with DKD and 87 T2DM patients without DKD. Additionally, 60 healthy participants without T2DM were also recruited as controls. Serum and urine samples were collected for HMGB1 analysis. Simultaneously, tumor necrosis factor receptor superfamily member 1A (TNFR-1) in serum and kidney injury molecule (KIM-1) in urine samples were evaluated for comparison. Results: Serum and urine HMGB1 levels were significantly higher in patients with DKD than in patients with T2DM and healthy controls. Additionally, serum HMGB1 levels significantly and positively correlated with serum TNFR-1 ( Conclusion: Serum HMGB1 was significantly correlated with DKD and disease severity. When the HMGB1 level was ≥27 ng/ml, the risk of renal progression increased sharply, indicating that serum HMGB1 can be used as a potential biomarker for the diagnosis of DKD progression.

Indexed as

Diabetes Mellitus, Type 2Diabetic NephropathiesHMGB1 ProteinBiomarkersHumansKidneyBiomarkersHMGB1 Proteinbiomarkerdiabetic kidney diseaseHMGB1progressionT2DM

Identifiers

PMID38481996
PMCPMC10932975
OpenAlexW4392235390

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.