Romero-Sánchez Consuelo, Ferrer-Santos Carlos, Abril Deisy, Acosta-Hernández Eduin, Ávila Juliette De, Ramos-Casallas Alejandro, Escobar Javier, Bautista-Molano Wilson, Jaimes Diego, Beltrán-Ostos Adriana, Bello-Gualtero Juan Manuel, Flórez-Sarmiento Cristian, Parra-Izquierdo Viviana, Calixto Omar Javier
Universidad Militar Nueva Granada, Facultad de Medicina, Programa de Reumatología, Grupo de Inmunología Clínica Aplicada, Bogotá, Colombia.
Universidad El Bosque, Grupo de Inmunología Celular y Molecular / INMUBO, Bogotá, Colombia.
Rev Alerg Mex. 2024 Feb 1;71(1):81. doi: 10.29262/ram.v71i1.1305.
To compare the diversity and composition of the gastrointestinal microbiome of patients with SpA.
MiSeq sequencing of the V3-V4 region of the 16S ribosomal RNA gene was performed on DNA isolated from stool. Patients with concurrent SpA and IBD were excluded. Differences were assessed for richness and diversity indices by QIIME 2™. Differences between means >0,2% with a p-value<0,05 were assumed significant. Institutional Ethics Committee endorsement.
69 individuals included, 49 with SpA (ankylosing spondylitis-AS 72,9%, psoriatic arthritis-PsA 18,8%, reactive arthritis-ReA 8,3%) 5 positive controls-dysbiosis and 15 controls-eubiosis. Conventional treatment in 42,9%, anti-IL-17 16,3% and anti-TNF 40,8%. By subtype, statistically significant differences in favour of AS were found for the diversity indices. AS vs PsA there was a difference in favour of AS for (p=0,002), (p=0,009), (p=0,008) and . AS vs ReA there was a difference in favour of AS for (p=0,009), (p=0.006), (p=0.031); (p=0,034). Diversity and richness showed differences in patients with high activity for Simpson's and Pielou's indices. In high activity, lower enrichment of (p= 0,0003), (p= 0,026) and (p=0,035) was found. The number of ASV was higher in the anti-IL-17 vs conventional group (p=0.025) and a trend between anti-IL-17 vs anti-TNF (p=0.09). In anti-TNF there was a lower proportion for (p=0.023), (p=0.030) and (p= 0.003). In anti IL-17, (p= 0.012) was decreased.
There are differences in microbial diversity for SpA subtypes. The level of disease activity is plausible to influence the composition of the faecal microbiota. Anti-TNFα treatment may influence the microbiome environment favouring restoration of the gut microbiota, while anti-IL-17 may maintain an inflammatory environment.
比较脊柱关节炎(SpA)患者胃肠道微生物群的多样性和组成。
对从粪便中分离的DNA进行16S核糖体RNA基因V3-V4区域的MiSeq测序。排除同时患有SpA和炎症性肠病(IBD)的患者。通过QIIME 2™评估丰富度和多样性指数的差异。均值差异>0.2%且p值<0.05被认为具有显著性。获得机构伦理委员会批准。
纳入69例个体,49例SpA患者(强直性脊柱炎-AS占72.9%,银屑病关节炎-PsA占18.8%,反应性关节炎-ReA占8.3%),5例阳性对照-菌群失调和15例对照-微生态平衡。42.9%接受传统治疗,16.3%接受抗IL-17治疗,40.8%接受抗TNF治疗。按亚型分析,多样性指数在AS组有统计学显著差异。AS与PsA相比,在(p=0.002)、(p=0.009)、(p=0.008)和方面,AS组有优势。AS与ReA相比,在(p=0.009)、(p=0.006)、(p=0.031);(p=0.034)方面,AS组有优势。对于辛普森指数和皮洛指数,疾病活动度高的患者的多样性和丰富度存在差异。在高疾病活动度时,发现(p=0.0003)、(p=0.026)和(p=0.035)的丰度较低。抗IL-17组的可操作分类单元(ASV)数量高于传统治疗组(p=0.025),抗IL-17组与抗TNF组之间有此趋势(p=0.09)。在抗TNF组中,(p=0.023)、(p=0.030)和(p=0.003)的比例较低。在抗IL-17组中,(p=0.012)降低。
SpA各亚型的微生物多样性存在差异。疾病活动水平可能影响粪便微生物群组成。抗TNFα治疗可能影响微生物群环境,有利于肠道微生物群恢复,而抗IL-17可能维持炎症环境。