Evidence map›Paper›PMID 36843591›Full record

ArticleFrontiers in endocrinology2023

The association of cell adhesion molecules and selectins (VCAM-1, ICAM-1, E-selectin, L-selectin, and P-selectin) with microvascular complications in patients with type 2 diabetes: A follow-up study.

Khalid Siddiqui, Teena P George, Muhammad Mujammami, Arthur Isnani, Assim A Alfadda

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

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0cells of the map it votes in
52citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

52 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Khalid SiddiquiStrategic Center for Diabetes Research, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Teena P GeorgeStrategic Center for Diabetes Research, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Muhammad MujammamiStrategic Center for Diabetes Research, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Arthur IsnaniObesity Research Center, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Assim A AlfaddaStrategic Center for Diabetes Research, College of Medicine, King Saud University, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Chronic hyperglycemia induces pathogenic changes in the vascular endothelium and leads to the development of microvascular complications in patients with type 2 diabetes mellitus. Early identification of markers of diabetes complications may help to minimize the risk of the development and progression of microvascular complications. Methods: This follow-up study was conducted in type 2 diabetic cohort aged between 30-70 years. Out of 160 eligible participants, 70 of them completed follow-up. Levels of cell adhesion molecules and selectins (VCAM-1, ICAM-1, E-selectin, L-selectin and P-selectin) at baseline and follow-up were measured using Randox Evidence biochip analyzer (UK). Development of microvascular complications (diabetic neuropathy, retinopathy and nephropathy) was evaluated. Results: During the follow-up (2 years, median), 31 (44.3%) developed diabetic neuropathy, 10 (14.3%) developed diabetic retinopathy and, 27 (38.6%) developed diabetic nephropathy. A significant difference in levels of cell adhesion molecules and selectins were found in type 2 diabetic patients with and without microvascular complications. Multiple logistic regression analysis reveals that baseline level of VCAM-1 is significantly associated with microvascular complications; diabetic neuropathy(p=0.028), retinopathy (p=0.007) and nephropathy(p=<0.001). Additionally, levels of P-selectin (p=0.05) and L-selectin (p=0.008) is associated with diabetic nephropathy while retinopathy associated with L-selectin (p=0.005) only. Conclusion: Cell adhesion molecules and selectins are indicators of microvascular complication among patients with type 2 diabetes (T2D). Association of these markers with the development of microvascular complications may provide additive information for developing strategies for diabetes management and prediction of microvascular complications.

Indexed as

Diabetes Mellitus, Type 2Diabetic NephropathiesDiabetic NeuropathiesDiabetic RetinopathyAdultAgedCell Adhesion MoleculesFollow-Up StudiesHumansIntercellular Adhesion Molecule-1L-SelectinMiddle AgedP-SelectinSelectinsVascular Cell Adhesion Molecule-1Cell Adhesion MoleculesIntercellular Adhesion Molecule-1L-SelectinP-SelectinSelectinsVascular Cell Adhesion Molecule-1adhesion moleculecomplicationsdiabetic nephropathydiabetic neuropathydiabetic retinopathy

Identifiers

PMID36843591
PMCPMC9948618

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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.