Evidence map›Paper›PMID 41296579›Full record

ArticleThe Indian journal of medical research2025

Association of cell adhesion molecules levels & single nucleotide polymorphisms with vaso-occlusive crisis in sickle cell disease: A cross sectional study.

Parul Gupta, Pankaj Asati, Asha Tiwari, Ravindra Kumar

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Article in The Indian journal of medical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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4 authors.

Parul GuptaDepartment of Genetics, ICMR-National Institute of Research in Tribal Health, Jabalpur, Madhya Pradesh, India.
Pankaj AsatiDepartment of Medicine, NSCB Medical College, Jabalpur, Madhya Pradesh, India.
Asha TiwariDepartment of Pediatrics, NSCB Medical College, Jabalpur, Madhya Pradesh, India.
Ravindra KumarDepartment of Genetics, ICMR-National Institute of Research in Tribal Health, Jabalpur, Madhya Pradesh, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & objectives Sickle cell disease (SCD) is a monogenic disorder characterised by aberrant haemoglobin production, leading to haemolytic anaemia and vaso-occlusive crises. Genetic variations and altered expression of cell adhesion molecules (CAMs) are implicated in disease pathogenesis. This cross-sectional study investigated the association between single nucleotide polymorphisms (SNPs) in the SELP, SELE, ICAM-1, and VCAM-1 genes and their protein levels in individuals with SCD. Methods A total of 140 individuals with SCD were recruited. Plasma levels of P-selectin, E-selectin, ICAM-1 and VCAM-1 were measured by ELISA method alongside a control group (n=10). The selected SNPs of SELP, SELE, ICAM-1, and VCAM-1 genes were identified through Sanger sequencing method. Results The expression of adhesion molecules were found to be significantly higher in SCD group as compared to control. Furthermore, the results showed significant associations between SNPs, SELE: c.109+138A>C (P<0.0001), SELE: c.422-25T>C (P<0.0001), and SELE: c.529+15T>C (P=<0.0001) with vaso-occlusive crises even after Bonferroni correction (corrected P=0.0025). Interpretation & conclusions Significant correlation observed between SELP, SELE, and VCAM-1 levels suggests complex interactions of these markers that may influence disease progression and identify potential therapeutic targets for managing SCD complications. Further studies are warranted to validate these findings in larger cohorts and explore the functional implications of the observed genetic and molecular associations in SCD.

Indexed as

Anemia, Sickle CellCell Adhesion MoleculesAdolescentAdultCross-Sectional StudiesE-SelectinFemaleGenetic Predisposition to DiseaseHumansIntercellular Adhesion Molecule-1MalePolymorphism, Single NucleotideP-SelectinVascular Cell Adhesion Molecule-1Cell Adhesion MoleculesE-SelectinICAM1 protein, humanIntercellular Adhesion Molecule-1P-SelectinSELE protein, humanSELP protein, humanVascular Cell Adhesion Molecule-1Cell adhesion moleculessickle cell diseasesingle nucleotide polymorphismsvaso-occlusive crisis

Identifiers

PMID41296579
PMCPMC12744576

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