Evidence map›Paper›PMID 41186884›Full record

Observational studyClinical rheumatology2026

The association between CD14 (C-159T) single-nucleotide polymorphism and Behcet's syndrome and its clinical manifestations in Egyptian patients, an observational case-control genetic association study.

Moustafa Ali Saad, Hala Ibrahem El Gendy, Olfat Shaker, Mariana Victor Philips, Yumn A Elsabagh

Abstract readObservational Study
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Observational study in Clinical rheumatology, 2026. 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

Authors and funding

5 authors.

Moustafa Ali SaadRheumatology and Clinical Immunology Unit, Internal Medicine Department, Kasr Alainy Faculty of Medicine, Cairo University, Cairo, Egypt. moustafa.ali.saad@kasralainy.edu.eg.ORCID http://orcid.org/0000-0001-6070-9407
Hala Ibrahem El GendyRheumatology and Clinical Immunology Unit, Internal Medicine Department, Kasr Alainy Faculty of Medicine, Cairo University, Cairo, Egypt.
Olfat ShakerMedical Biochemistry and Molecular Biology Department, Kasr Alainy Faculty of Medicine, Cairo University, Cairo, Egypt.ORCID http://orcid.org/0000-0002-3031-3599
Mariana Victor PhilipsDepartment of Internal Medicine, Faculty of Medicine, Cairo University, Cairo, Egypt.
Yumn A ElsabaghRheumatology and Clinical Immunology Unit, Internal Medicine Department, Kasr Alainy Faculty of Medicine, Cairo University, Cairo, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCluster of differentiation 14 (CD14) molecules are immune cell surface molecules that bind and display lipopolysaccharides (LPSs) of gram-negative bacteria to Toll-like receptor 4 (TLR4), facilitating LPS-induced immune cell activation. The CD14 promoter polymorphism C-159T is positively correlated with CD14, and homozygous carriers of the T allele have a significant increase in soluble and membrane-bound CD14.

objectiveTo assess the C-159T polymorphism in Behcet patients compared to controls, and to study its relationship with disease manifestations and activity.

methodsFifty-one adult Egyptian patients with Behcet's syndrome and another 51 healthy controls were recruited. Behcet's syndrome activity was assessed. A blood sample was obtained from each participant for DNA extraction. The extracted DNA was used to determine the C-159T polymorphism in the CD14 promoter gene (rs2569190) using real-time polymerase chain reaction.

resultsThe prevalence of the TT genotype was higher in Behcet patients (23.7%) in comparison to the controls (8%) (OR = 5.3, P value = 0.01). The prevalence of the T allele was higher in Behcet patients (49.1%) in comparison to the controls (31.4%) (OR = 2.1, P value = 0.01). The skin erythema was found to be significantly (P value = 0.003) higher in frequency among the TT genotype (58.3%) compared to the CT genotype (26.9%). Moreover, the skin pustules were found to be significantly (P value = 0.01) higher in frequency among the TT genotype (41.6%) compared to the CT genotype (11.5%).

conclusionCD14 (C-159T) polymorphism is associated with an increased risk of developing Behcet's syndrome and is correlated with its dermatological manifestations. Key points • Behcet's syndrome is a variable-vessel vasculitis in which aberrant innate immunity is integral to the pathogenesis of the disease. • CD14 molecules recognize pathogens with subsequent activation of innate immunity. • The CD14 promoter gene C-159T single-nucleotide polymorphism increases the susceptibility to Behcet's syndrome. • The C-159T polymorphism correlates with skin manifestations of Behcet's syndrome.

Indexed as

Behcet SyndromeLipopolysaccharide ReceptorsPolymorphism, Single NucleotideAdultAllelesCase-Control StudiesEgyptFemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseGenotypeHumansMaleMiddle AgedPromoter Regions, GeneticCD14 protein, humanLipopolysaccharide ReceptorsBehcet syndromeC-159T SNPCD14SNP

Identifiers

PMID41186884
PMCPMC12855428

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