Taylor Brandie D, Darville Toni, Ferrell Robert E, Ness Roberta B, Kelsey Sheryl F, Haggerty Catherine L
Department of Epidemiology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Department of Pediatrics, University of North Carolina Chapel Hill, Chapel Hill, North Carolina, USA.
Sex Transm Infect. 2014 Nov;90(7):563-6. doi: 10.1136/sextrans-2014-051524. Epub 2014 May 21.
Bacterial vaginosis (BV) is a common condition associated with serious complications including pelvic inflammatory disease (PID). However, the pathogenesis of BV is poorly understood. Toll-like receptors (TLR) are responsible for microbial recognition and elimination through inflammatory responses. TLR variants have been implicated in infectious and inflammatory diseases and may be involved in BV pathogenesis. We conducted a cross-sectional study to determine if TLR variants are associated with BV.
Logistic regression was used to test associations between 14 variants assayed in 6 genes (TLR1, TLR2, TLR4, TLR6, TIRAP and MyD88) and BV/intermediate flora among 192 African-American women with clinical PID from the PID Evaluation and Clinical Health (PEACH) Study. Additionally, we examined associations between variants and endometrial BV-associated anaerobes. To account for multiple comparisons a permutated p<0.003 was used to determine statistical significance.
African-American women with PID carrying the AA genotype for TLR2 SNP rs1898830 had a threefold increased rate of BV/intermediate flora (OR 2.9, 95% CI 1.2 to 7.3). This was not significant after accounting for multiple comparisons (p=0.0201). TLR2 variants rs1898830, rs11938228 and rs3804099 were associated with increased endometrial anaerobic gram-negative rods (p=0.0107, p=0.0076 p=0.0121), anaerobic non-pigmented Gram-negative rods (p=0.0231, p=0.0083, p=0.0044), and anaerobic Gram-positive cocci (p=0.0596, p=0.0640, p=0.1459).
Among African-American women with PID, we observed trends between TLR2 variants, BV/intermediate flora, and BV-associated microbes. This provides some insight into BV pathogenesis. As not all BV-associated microbes may lead to pathology, future studies should focus on associations between TLR variants and individual BV-associated microbes.
细菌性阴道病(BV)是一种常见病症,与包括盆腔炎(PID)在内的严重并发症相关。然而,BV的发病机制尚不清楚。Toll样受体(TLR)负责通过炎症反应识别和清除微生物。TLR变异体与感染性和炎症性疾病有关,可能参与BV的发病机制。我们进行了一项横断面研究,以确定TLR变异体是否与BV相关。
采用逻辑回归分析,对192名来自PID评估与临床健康(PEACH)研究的患有临床PID的非裔美国女性中,6个基因(TLR1、TLR2、TLR4、TLR6、TIRAP和MyD88)检测的14个变异体与BV/中间菌群之间的关联进行测试。此外,我们还研究了变异体与子宫内膜BV相关厌氧菌之间的关联。为了考虑多重比较,使用经置换的p<0.003来确定统计学显著性。
携带TLR2单核苷酸多态性(SNP)rs1898830的AA基因型的患有PID的非裔美国女性,其BV/中间菌群发生率增加了两倍(比值比2.9,95%置信区间1.2至7.3)。在考虑多重比较后,这一结果无统计学显著性(p=0.0201)。TLR2变异体rs1898830、rs11938228和rs3804099与子宫内膜厌氧革兰氏阴性杆菌增加有关(p=0.0107,p=0.0076,p=0.0121),与厌氧无色素革兰氏阴性杆菌增加有关(p=0.0231,p=0.0083,p=0.0044),与厌氧革兰氏阳性球菌增加有关(p=0.0596,p=0.0640,p=0.1459)。
在患有PID的非裔美国女性中,我们观察到TLR2变异体、BV/中间菌群和BV相关微生物之间的趋势。这为BV的发病机制提供了一些见解。由于并非所有BV相关微生物都可能导致病变,未来的研究应聚焦于TLR变异体与单个BV相关微生物之间的关联。