Evidence map›Paper›PMID 39621725›Full record

ArticlePloS one2024

Activity of glucose-6-phosphate dehydrogenease and its correlation with inflammatory factors in diabetic retinopathy.

Dan Liu, Chuchu Cheng, Lan Zhou, Qiqiao Zeng, Tao Zi, Gongyi Chen, Hongyan Sun, Cunzi Li, Jun Wang, Ming-Ming Yang

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 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

10 authors.

Dan LiuDepartment of Ophthalmology, The Second Clinical Medical College, Jinan University, Shenzhen, China.ORCID 0009-0002-2738-5679
Chuchu ChengDepartment of Endocrinology, The Second People's Hospital of Futian District, Shenzhen, China.
Lan ZhouDepartment of Ophthalmology, The Shenzhen People's Hospital, Shenzhen, China.
Qiqiao ZengDepartment of Ophthalmology, The Shenzhen People's Hospital, Shenzhen, China.
Tao ZiDepartment of Ophthalmology, The Shenzhen People's Hospital, Shenzhen, China.
Gongyi ChenDepartment of Ophthalmology, The Shenzhen People's Hospital, Shenzhen, China.
Hongyan SunDepartment of Ophthalmology, The Shenzhen People's Hospital, Shenzhen, China.
Cunzi LiDepartment of Ophthalmology, The Shenzhen People's Hospital, Shenzhen, China.
Jun WangDepartment of Endocrinology, The Shenzhen People's Hospital, Shenzhen, China.
Ming-Ming YangDepartment of Ophthalmology, The Shenzhen People's Hospital, Shenzhen, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis study aims to explore glucose-6-phosphate dehydrogenase (G6PD) activity in diabetic retinopathy (DR) and its correlation with inflammatory factors, elucidating the regulatory role of G6PD in DR pathology.

methodsA total of 151 T2DM patients were divided into three groups: diabetes without retinopathy (DNR, n = 59), non-proliferative retinopathy (NPDR, n = 46) and proliferative retinopathy (PDR, n = 49). Plasma G6PD activity was measured by a Randox G6PD kit and compared between these groups. Then the G6PD activity was correlated with inflammatory cytokines and metabolic parameters in these patients. A STZ-induced diabetic rat model was established, G6PD activity was validated by western blot and immunofluorescence staining in the retina of this model.

resultsPlasma G6PD activity decreased in the order of DNR, NPDR and PDR groups (P<0.01). G6PD activity was negatively correlated with IL-6, IL-8, TNF-α, cholesterol, and LDL (r = -0.1625, -0.1808, -0.1865, -0.1747, r = -0.1807, P<0.05). Multiple regression analysis showed TNF-α, IL-6, and LDL were independent related factors for G6PD. Logistic regression analysis showed G6PD, triglyceride, cholesterol, IL-8, TNF-α, and macular edema were influencing factors for T2DM with DR. Western Blot analysis indicated a significant reduction of G6PD expression in the retina, and immunofluorescence staining showed distribution of G6PD especially in the retinal endothelium cell decreased.

conclusionG6PD may play an important role in DR occurrence and progression, with decreased expression correlating closely with lipid metabolism and inflammatory factors.

Indexed as

Diabetic RetinopathyGlucosephosphate DehydrogenaseAgedAnimalsCytokinesDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2FemaleHumansInterleukin-6MaleMiddle AgedRatsRats, Sprague-DawleyRetinaTumor Necrosis Factor-alphaCytokinesGlucosephosphate DehydrogenaseInterleukin-6Tumor Necrosis Factor-alpha

Identifiers

PMID39621725
PMCPMC11611225

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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.