High-Risk PNPLA3 rs738409 Genotype Is Associated with Higher Concentrations of CCL2 in Liver Transplant Candidates with Alcoholic End-Stage Liver Disease

被引:0
作者
Budimir Bekan, Ivan [1 ]
Sisl, Dino [2 ,3 ]
Sucur, Alan [2 ,3 ]
Bainrauch, Ana [4 ]
Lang, Valerija Bralic [5 ,6 ]
Planinic, Pavao [7 ]
Kovacic, Natasa [2 ,8 ]
Grcevic, Danka [2 ,3 ]
Mrzljak, Anna [9 ,10 ]
Kelava, Tomislav [2 ,3 ]
机构
[1] Merkur Univ Hosp, Dept Surg, Zagreb 10000, Croatia
[2] Univ Zagreb, Croatian Inst Brain Res, Lab Mol Immunol, Zagreb 10000, Croatia
[3] Univ Zagreb, Sch Med, Dept Physiol & Immunol, Zagreb 10000, Croatia
[4] Merkur Univ Hosp, Dept Internal Med, Zagreb 10000, Croatia
[5] Private Family Phys Off Zagreb, Zagreb 10000, Croatia
[6] Univ Zagreb, Sch Med, Dept Family Med, Zagreb 10000, Croatia
[7] Univ Mostar, Sch Med, Dept Physiol, Mostar 88000, Bosnia & Herceg
[8] Univ Zagreb, Sch Med, Dept Anat, Zagreb 10000, Croatia
[9] Univ Zagreb, Sch Med, Zagreb 10000, Croatia
[10] Univ Zagreb, Univ Hosp Ctr Zagreb, Dept Gastroenterol & Hepatol, Zagreb 10000, Croatia
来源
MEDICINA-LITHUANIA | 2025年 / 61卷 / 07期
关键词
cytokine; alcoholic liver disease; single nucleotide polymorphism; liver transplantation; PNPLA3; 148M; chemokine (C-C motif) ligand 2; MONOCYTE CHEMOATTRACTANT PROTEIN-1; EXPRESSION; ADIPOSITY; CYTOKINES; SEVERITY;
D O I
10.3390/medicina61071293
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and Objectives: Patients with GG rs738409 patatin-like phospholipase domain-containing protein 3 (PNPLA3) genotype (148M variant) have greater risk to develop end-stage liver disease and its associated clinical complications, including hepatocellular carcinoma (HCC). We aimed to analyze the association between the PNPLA3 genotype and augmented inflammatory response in transplant candidates with end-stage alcoholic liver disease (ALD). Materials and Methods: Concentrations of 13 cytokines were measured in 106 end-stage ALD patients without HCC (40 with CC, 40 with CG, and 26 with GG genotype), 35 end-stage ALD patients with HCC, and 19 control patients by cytometric bead array. Results: We found significantly higher concentrations of IL-1, IFN-alpha, IFN-gamma, TNF-alpha, IL-6, CXCL8, IL-10, IL-12, IL-32, and IL-33 in patients with ALD compared to controls, while the concentration of CCL2 was significantly lower. No differences were observed in the concentration of IL-17 and IL-18. ALD patients with and without HCC had similar cytokine concentrations (p > 0.05 for all comparisons). End-stage ALD patients without HCC of the GG genotype had significantly higher CCL2 concentrations (212.6 [135.9-264.9] pg/mL) compared to end-stage ALD patients without HCC carrying the CC/CG genotypes (141.3 [104.1-201.6] pg/mL, p = 0.002, Mann-Whitney). No significant differences across the genotypes were found for the remaining measured cytokines (p > 0.05). GG carriers also had significantly higher levels of AST and ALT, and lower platelet counts. Conclusions: End-stage ALD patients without HCC who carry the PNPLA3 GG genotype have relatively higher CCL2 levels compared to those with the CC or CG genotypes. Relatively elevated CCL2 concentrations in GG patients might contribute to their increased risk of developing clinical complications compared to CC/CG patients.
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页数:15
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