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08 June 2022: Clinical Research

Association Between Variants of the Mannose-Binding Lectin 2 Gene and Susceptibility to Sepsis in the Hainan Island

Shaowen Cheng 123ABCDEFG* , Junyu Zhu 4ABCDE* , Xini Liu 5CDEF* , Jian Yang 12AEF , Yudie Wang 6BCD , Wei Zhang 6BCD , Zhihua Hu 7AEF* , Jiemiao Ouyang 8ADF* , Huaping Liang 4AEFG*

DOI: 10.12659/MSM.936134

Med Sci Monit 2022; 28:e936134

Table 3 Genotypic and allelic frequency distribution of rs1800450 in the sepsis group and non-sepsis group. P=0.014 for dominant association (GA+AA vs GG). P=0.971 for recessive association (AA vs GA+GG).

GenotypeSepsis group n/%Non-sepsis group n/%Pχ2OR95% CI
271310
GG193 (71.2)248 (80.0)
GA72 (26.6)55 (17.7)0.0106.6221.6821.130–2.505
AA6 (2.2)7 (2.3)
G458 (84.5)551 (87.9)
A84 (15.5)69 (12.1)0.0284.8281.4651.041–2.061
GA+AA78 (28.8)62 (20.0)0.0146.0980.6190.422–0.907
GA+GG265 (97.8)303 (97.7)0.9710.011.0200.339–3.074
P=0.014 for dominant association (GA+AA vs GG). P=0.971 for recessive association (AA vs GA+GG). The frequency of a GA genotype was significantly higher in the sepsis group than in the non-sepsis group (P=0.010). Allele frequency analysis also showed that the frequency of the A allele in the sepsis group was much higher than that in the non-sepsis group (P=0.029; Table 3). χ analysis showed that GA genotype patients were 1.682 times more likely to develop sepsis than GG genotype patients (OR=1.682, 95% CI=1.340–2.505). Patients who carried the A allele were more likely to acquire sepsis than G allele carriers (OR=1.465, 95% CI=1.041–2.061), which means that the variation of rs1800450, G→A increased the incidence of sepsis (Table 3).

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Medical Science Monitor eISSN: 1643-3750
Medical Science Monitor eISSN: 1643-3750