Connelly Tara M, Choi Christine S, Berg Arthur S, Harris Leonard, Coble Joel, Koltun Walter A
Division of Colon and Rectal Surgery, Department of Surgery, College of Medicine, The Pennsylvania State University, Hershey, Pennsylvania.
Department of Public Health Sciences, College of Medicine, The Pennsylvania State University, Hershey, Pennsylvania.
J Surg Res. 2017 Jun 15;214:262-269. doi: 10.1016/j.jss.2017.02.030. Epub 2017 Feb 27.
Diverticulitis (DD) and Crohn's disease (CD) have overlapping features including bowel structuring, inflammation, and infection. Tumor necrosis superfamily 15 (TNFSF15) is an immunoregulatory, anti-angiogenic gene. CD has been previously associated with a haplotype of five TNFSF15 single-nucleotide polymorphism alleles: rs3810936 (G allele), rs6478108 (A), rs6478109 (G), rs7848647 (G), and rs7869487 (A). We aimed to determine the TNFSF15 risk haplotype for DD versus controls with a subgroup analysis of youthful DD patients (aged ≤55 y) versus older controls (aged ≥55 y).
A total of 148 diverticulitis patients (90 aged ≤55 y) and 200 controls (87 aged ≥55 y) were genotyped using our custom-designed Illumina Veracode microarray chip. Genotypes from rs3810936, rs6478108, rs6478109, rs7848647, rs7869487 and two additional TNFSF15 single nucleotide polymorphisms, rs3810936 and rs11554257, were analyzed. PHASE version 2.1, R with HaploStats and the Broad Institute's Haploview program were used for statistics and imputed haplotype frequency. Permutation corrected for multiple comparisons.
The CD GAGGA haplotype was significantly associated with diverticulitis (P = 0.03) in the all DD versus all controls comparison. A second haplotype, rs6478108 (A), rs6478109 (G), rs7869487 (A), and rs4263839 (G), was also associated with DD in this cohort (P = 0.025). A third haplotype rs6478108 (A), rs6478109 (G), rs7848647 (G) and rs7869487 (A), rs4263839 (G) was demonstrated in the DD < 55 versus controls >55 comparison (P = 0.045).
Distinct but overlapping TNFSF15 haplotypes were demonstrated in diverticulitis patients versus healthy controls when compared with the known Crohn's risk haplotype suggesting similar but distinct genetic predispositions. This study strengthens the role for a genetic predisposition to diverticulitis that involves the TNFSF15 gene.
憩室炎(DD)和克罗恩病(CD)具有一些重叠特征,包括肠道结构改变、炎症和感染。肿瘤坏死超家族15(TNFSF15)是一个免疫调节、抗血管生成基因。此前发现CD与TNFSF15的五个单核苷酸多态性等位基因的单倍型相关:rs3810936(G等位基因)、rs6478108(A)、rs6478109(G)、rs7848647(G)和rs7869487(A)。我们旨在确定DD相对于对照组的TNFSF15风险单倍型,并对年轻的DD患者(年龄≤55岁)与老年对照组(年龄≥55岁)进行亚组分析。
使用我们定制设计的Illumina Veracode微阵列芯片对148例憩室炎患者(90例年龄≤55岁)和200例对照(87例年龄≥55岁)进行基因分型。分析了rs3810936、rs6478108、rs6478109、rs7848647、rs7869487以及另外两个TNFSF15单核苷酸多态性rs3810936和rs11554257的基因型。使用PHASE 2.1版、带有HaploStats的R软件以及布罗德研究所的Haploview程序进行统计和推算单倍型频率。采用置换法校正多重比较。
在所有DD患者与所有对照的比较中,CD的GAGGA单倍型与憩室炎显著相关(P = 0.03)。在该队列中,另一个单倍型,即rs6478108(A)、rs6478109(G)、rs7869487(A)和rs4263839(G),也与DD相关(P = 0.025)。在年龄<55岁的DD患者与年龄>55岁的对照的比较中,发现了第三个单倍型rs6478108(A)、rs6478109(G)、rs7848647(G)以及rs7869487(A)、rs4263839(G)(P = 0.045)。
与已知的克罗恩病风险单倍型相比,憩室炎患者与健康对照中显示出不同但有重叠的TNFSF15单倍型,提示存在相似但不同的遗传易感性。本研究强化了TNFSF15基因在憩室炎遗传易感性中的作用。