Evidence map›Paper›PMID 42031905›Full record

Observational studyScientific reports2026

Oxymatrine regulates SPHKS/S1P signaling pathway in diabetic retinopathy: an observational clinical cohort study.

Jin Xu, Yan Li, Ge-Yao Qi, Juan Feng, Fei Wang

Abstract readObservational Study
In one paragraph

Observational study in Scientific reports, 2026. 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

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

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

5 authors.

Jin XuDepartment of Endocrinology, The 940th Hospital of Joint Logistic Support Force of Chinese People's Liberation Army (PLA), Lanzhou City, Gansu Province, 730050, China.ORCID http://orcid.org/0000-0002-4964-9404
Yan LiDepartment of Endocrinology, The 940th Hospital of Joint Logistic Support Force of Chinese People's Liberation Army (PLA), Lanzhou City, Gansu Province, 730050, China.
Ge-Yao QiDepartment of Internal Medicine, No. 32186 Unit Hospital of Chinese People's Liberation Army (PLA), Baoding City, Hebei Province, 071000, China.ORCID http://orcid.org/0000-0002-9124-8049
Juan FengDepartment of Cardiology, The 940th Hospital of Joint Logistic Support Force of Chinese People's Liberation Army (PLA), No. 333, Middle Section of South Binhe Road, Qilihe District, Lanzhou City, Gansu Province, 730050, China.
Fei WangDepartment of Cardiology, The 940th Hospital of Joint Logistic Support Force of Chinese People's Liberation Army (PLA), No. 333, Middle Section of South Binhe Road, Qilihe District, Lanzhou City, Gansu Province, 730050, China. wangfei940@sina.com.

Funding

Project of Natural Science Foundation of Gansu Province 22JR5RA010Project of Science and Technology Plan of Lanzhou City 2023-ZD-168
6 · The paper itself

Abstract

backgroundThe SPHKS/S1P pathway has a complex yet close association with the progression of diabetic retinopathy (DR). Oxymatrine (OMT), is believed to potentially regulate this pathway; however, systematic clinical evidence remains insufficient.

methodsA total of 84 DR cases was finally included in the observation cohort, among which 41 cases were assigned to the OMT group and 43 cases to the non-OMT group. Additionally, 20 non-DR cases were included as blank controls. The levels of 4 target proteins, including S1P, VEGF, SPHK1, and SPHK2, were detected in the peripheral blood of cases in each group. The temporal changes in these protein levels were compared between the OMT group and the non-OMT group. Furthermore, the progression of DR between the two groups was statistically analyzed before and after treatment.

resultsCompared with non-DR cases, the levels of 4 target proteins of DR cases were significantly increased. No statistically significant differences in the levels of these proteins were observed between the OMT group and the non-OMT group before treatment; the temporal change trends in the expression levels of these proteins in the OMT group were significantly lower than those in the non-OMT group after treatment. However, no statistically significant differences were found between the OMT group and the non-OMT group in terms of DR progression.

conclusionOMT could inhibit the activity of the SPHKS/S1P pathway and downregulate the expression of key proteins; however, the clinical efficacy of OMT in relieving the progression of DR remained unclear in this study.

Indexed as

AlkaloidsDiabetic RetinopathyPhosphotransferases (Alcohol Group Acceptor)QuinolizinesSignal TransductionSphingosineAgedCohort StudiesFemaleHumansMaleMatrinesMiddle AgedSphingosine KinaseAlkaloidsMatrinesoxymatrinePhosphotransferases (Alcohol Group Acceptor)QuinolizinesSphingosineSphingosine KinaseDRMicrovascular proliferationOMTSPHKS/S1P pathway

Identifiers

PMID42031905
PMCPMC13276429

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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.