Research Center of Clinical Pharmacology, The First Affiliated Hospital of Yunnan University of Chinese Medicine, Kunming, China.
Department of Clinical Pharmacy, 920th Hospital of Joint Logistics Support Force of People's Liberation Army, Kunming, China.
Cytokine. 2023 Oct;170:156312. doi: 10.1016/j.cyto.2023.156312. Epub 2023 Aug 3.
Recently, increasing evidence has demonstrated that IL-10 single nucleotide polymorphisms (SNPs) are associated with the risk of acute leukemia (AL), but the findings of different articles remain controversial. Thus, we performed a meta-analysis to further investigate the exact roles of IL-10 SNPs in AL susceptibility.
Six common Chinese and English databases were utilized to retrieve eligible studies. The strength of the association was assessed by calculating odds ratios and 95 % confidence intervals. All analyses were carried out using Review Manager (version 5.3) and STATA (version 15.1). The registered number of this research is CRD42022373362.
A total of 6391 participants were enrolled in this research. The results showed that the AG genotype of rs1800896 increased AL risk in the heterozygous codominant model (AG vs. AA, OR = 1.41, 95 % CI = 1.04-1.92, P = 0.03) and overdominant model (AG vs. AA + GG, OR = 1.32, 95 % CI = 1.04-1.70, P = 0.03). In the subgroup analysis, associations between the G allele, GG genotype, AG genotype, AG + GG genotype of rs1800896 and increased AL risk were also observed in the mixed population based on allelic, homozygote codominant, heterozygous codominant, dominant, and overdominant models. Furthermore, an association between the AC genotype of rs1800872 and increased AL risk was observed in the Caucasian population in the overdominant model. However, the rs1800871, rs3024489 and rs3024493 polymorphisms did not affect AL risk.
IL-10 rs1800896 and rs1800872 affected the susceptibility of AL and therefore may be biomarkers for early screening and risk prediction of AL.
最近,越来越多的证据表明白细胞介素-10(IL-10)单核苷酸多态性(SNP)与急性白血病(AL)的风险相关,但不同研究的结果仍存在争议。因此,我们进行了一项荟萃分析,以进一步探讨 IL-10 SNP 与 AL 易感性的确切关系。
我们使用 6 个常用的中文和英文数据库检索了符合条件的研究。通过计算比值比(OR)和 95%置信区间(CI)来评估关联的强度。所有分析均使用 Review Manager(版本 5.3)和 STATA(版本 15.1)进行。本研究的注册号为 CRD42022373362。
共有 6391 名参与者纳入本研究。结果表明,rs1800896 的 AG 基因型在杂合子显性模型(AG 与 AA,OR=1.41,95%CI=1.04-1.92,P=0.03)和超显性模型(AG 与 AA+GG,OR=1.32,95%CI=1.04-1.70,P=0.03)中增加了 AL 的风险。在亚组分析中,基于等位基因、纯合子显性、杂合子显性、显性和超显性模型,rs1800896 的 G 等位基因、GG 基因型、AG 基因型、AG+GG 基因型与 AL 风险增加之间也存在关联。此外,在高加索人群中,rs1800872 的 AC 基因型在超显性模型中与 AL 风险增加相关。然而,rs1800871、rs3024489 和 rs3024493 多态性并未影响 AL 风险。
IL-10 rs1800896 和 rs1800872 影响 AL 的易感性,因此可能是 AL 早期筛查和风险预测的生物标志物。