Tokuno Hidetaka, Itoga Tatsuya, Kasuga Jumpei, Okuma Kana, Hasuko Kazumi, Masuyama Hiroaki, Benno Yoshimi
Symbiosis Solutions Inc., Tokyo, Japan.
Benno Institute for Gut Microflora, Saitama, Japan.
Front Microbiol. 2023 Jan 26;14:1035002. doi: 10.3389/fmicb.2023.1035002. eCollection 2023.
The relationship between the human gut microbiota and disease is of increasing scientific interest. Previous investigations have focused on the differences in intestinal bacterial abundance between control and affected groups to identify disease biomarkers. However, different types of intestinal bacteria may have interacting effects and thus be considered biomarker complexes for disease. To investigate this, we aimed to identify a new kind of biomarker for atopic dermatitis using structural equation modeling (SEM). The biomarkers identified were latent variables, which are complex and derived from the abundance data for bacterial marker candidates. Groups of females and males classified as healthy participants [normal control (NC) (female: 321 participants, male: 99 participants)], and patients afflicted with atopic dermatitis only [AS (female: 45 participants, male: 13 participants)], with atopic dermatitis and other diseases [AM (female: 75 participants, male: 34 participants)], and with other diseases but without atopic dermatitis [OD (female: 1,669 participants, male: 866 participants)] were used in this investigation. The candidate bacterial markers were identified by comparing the intestinal microbial community compositions between the NC and AS groups. In females, two latent variables (lv) were identified; for lv1, the associated components (bacterial genera) were , , and , while for lv2, the associated components were , , and . There was a significant difference in the lv2 scores between the groups with atopic dermatitis (AS, AM) and those without (NC, OD), and the genera identified for lv2 are associated with the suppression of inflammatory responses in the body. A logistic regression model to estimate the probability of atopic dermatitis morbidity with lv2 as an explanatory variable had an area under the curve (AUC) score of 0.66 when assessed using receiver operating characteristic (ROC) analysis, and this was higher than that using other logistic regression models. The results indicate that the latent variables, especially lv2, could represent the effects of atopic dermatitis on the intestinal microbiome in females. The latent variables in the SEM could thus be utilized as a new type of biomarker. The advantages identified for the SEM are as follows: (1) it enables the extraction of more sophisticated information when compared with models focused on individual bacteria and (2) it can improve the accuracy of the latent variables used as biomarkers, as the SEM can be expanded.
人类肠道微生物群与疾病之间的关系正日益引起科学界的关注。以往的研究主要集中在对照组和患病组之间肠道细菌丰度的差异上,以确定疾病生物标志物。然而,不同类型的肠道细菌可能具有相互作用的影响,因此可被视为疾病的生物标志物复合物。为了对此进行研究,我们旨在使用结构方程模型(SEM)来识别一种新的特应性皮炎生物标志物。所识别的生物标志物是潜在变量,它们复杂且源自细菌标志物候选物的丰度数据。本研究使用了被分类为健康参与者的女性和男性群体[正常对照(NC)(女性:321名参与者,男性:99名参与者)],仅患有特应性皮炎的患者[AS(女性:45名参与者,男性:13名参与者)],患有特应性皮炎和其他疾病的患者[AM(女性:75名参与者,男性:34名参与者)],以及患有其他疾病但无特应性皮炎的患者[OD(女性:1669名参与者,男性:866名参与者)]。通过比较NC组和AS组之间的肠道微生物群落组成来识别候选细菌标志物。在女性中,识别出了两个潜在变量(lv);对于lv1,相关成分(细菌属)是 、 和 ,而对于lv2,相关成分是 、 和 。患有特应性皮炎的组(AS、AM)和未患特应性皮炎的组(NC、OD)之间的lv2得分存在显著差异,并且为lv2识别出的属与体内炎症反应的抑制相关。以lv2作为解释变量来估计特应性皮炎发病概率的逻辑回归模型,在使用受试者工作特征(ROC)分析进行评估时,曲线下面积(AUC)得分为0.66,这高于使用其他逻辑回归模型时的得分。结果表明,潜在变量,尤其是lv2,可以代表特应性皮炎对女性肠道微生物群的影响。因此,SEM中的潜在变量可被用作一种新型生物标志物。为SEM确定的优点如下:(1)与关注单个细菌的模型相比,它能够提取更复杂的信息;(2)它可以提高用作生物标志物的潜在变量的准确性,因为SEM可以扩展。