Tuberculosis Research Unit, National Heart and Lung Institute, Imperial College London, London, UK.
Thorax. 2013 Mar;68(3):221-9. doi: 10.1136/thoraxjnl-2012-201824. Epub 2012 Sep 27.
Emerging evidence suggests that Mycobacterium tuberculosis (Mtb) lineage and host ethnicity can determine tuberculosis (TB) clinical disease patterns but their relative importance and interaction are unknown.
We evaluated prospectively collected TB surveillance and Mtb strain typing data in an ethnically heterogeneous UK population. Lineage assignment was denoted using 15-loci mycobacterial interspersed repetitive units containing variable numbers of tandem repeats (MIRU-VNTR) and MIRU-VNTRplus. Geographical and ethnic associations of the six global Mtb lineages were identified and the influence of lineage and demographic factors on clinical phenotype were assessed using multivariate logistic regression.
Data were available for 1070 individuals with active TB which was pulmonary only, extrapulmonary only and concurrent pulmonary-extrapulmonary in 52.1%, 36.9% and 11.0% respectively. The most prevalent lineages were Euro-American (43.7%), East African Indian (30.2%), Indo-Oceanic (13.6%) and East Asian (12.2%) and were geo-ethnically restricted with, for example, Indian subcontinent ethnicity inversely associated with Euro-American lineage (OR 0.23; 95% CI 0.14 to 0.39) and positively associated with the East African-Indian lineage (OR 4.04; 95% CI 2.19 to 7.45). Disease phenotype was most strongly associated with ethnicity (OR for extrathoracic disease 21.14 (95% CI 6.08 to 73.48) for Indian subcontinent and 14.05 (3.97 to 49.65) for Afro-Caribbean), after adjusting for lineage. With East Asian lineage as the reference category, the Euro-American (OR 0.54; 95% CI 0.32 to 0.91) and East-African Indian (OR 0.50; 95% CI 0.29 to 0.86) lineages were negatively associated with extrathoracic disease, compared with pulmonary disease, after adjusting for ethnicity.
Ethnicity is a powerful determinant of clinical TB phenotype independently of mycobacterial lineage and the role of ethnicity-associated factors in pathogenesis warrants investigation.
新出现的证据表明,结核分枝杆菌(Mycobacterium tuberculosis,Mtb)谱系和宿主种族可以决定结核病(tuberculosis,TB)的临床疾病模式,但它们的相对重要性和相互作用尚不清楚。
我们评估了英国一个种族多样化人群中前瞻性收集的结核病监测和 Mtb 菌株分型数据。使用含有可变数量串联重复(mycobacterial interspersed repetitive units containing variable numbers of tandem repeats,MIRU-VNTR)和 MIRU-VNTRplus 的 15 个基因座分枝杆菌间隔重复单位来指定谱系。确定了 6 个全球 Mtb 谱系的地理和种族关联,并使用多变量逻辑回归评估了谱系和人口统计学因素对临床表型的影响。
1070 名活动性肺结核患者的数据可用,其中 52.1%为单纯肺结核、36.9%为单纯肺外结核、11.0%为肺外合并肺结核。最常见的谱系是欧亚裔(43.7%)、东非印度裔(30.2%)、印度-太平洋裔(13.6%)和东亚裔(12.2%),它们在地理和种族上受到限制,例如,与欧亚裔谱系呈负相关(比值比 0.23;95%置信区间 0.14 至 0.39),与东非-印度裔谱系呈正相关(比值比 4.04;95%置信区间 2.19 至 7.45)。在调整了谱系后,疾病表型与种族的关联最为密切(印度次大陆人群发生胸腔外疾病的比值比为 21.14(95%置信区间 6.08 至 73.48),加勒比黑人人群为 14.05(3.97 至 49.65))。以东亚裔谱系为参考类别,与肺结核相比,欧亚裔(比值比 0.54;95%置信区间 0.32 至 0.91)和东非-印度裔(比值比 0.50;95%置信区间 0.29 至 0.86)谱系与胸腔外疾病呈负相关,在调整了种族后。
种族是临床结核病表型的一个强有力决定因素,独立于分枝杆菌谱系,种族相关因素在发病机制中的作用值得进一步研究。