González-Mercado Velda J, Pérez-Santiago Josué, Lyon Debra, Dilán-Pantojas Israel, Henderson Wendy, McMillan Susan, Groer Maureen, Kane Brad, Marrero Sara, Pedro Elsa, Saligan Leorey N
College of Nursing, University of South Florida, Tampa, FL, USA.
Puerto Rico Omics Center, Comprehensive Cancer Center, University of Puerto Rico, San Juan, PR, USA.
Adv Med. 2020 Feb 7;2020:6375876. doi: 10.1155/2020/6375876. eCollection 2020.
The objectives of this proof of concept study were to (a) examine the temporal changes in fatigue and diversity of the gut microbiome over the course of chemoradiotherapy (CRT) in adults with rectal cancers; (b) investigate whether there are differences in diversity of the gut microbiome between fatigued and nonfatigued participants at the middle and at the end of CRT; and (c) investigate whether there are differences in the relative abundance of fecal microbiota at the phylum and genus levels between fatigued and nonfatigued participants at the middle and at the end of CRT.
Stool samples and symptom ratings were collected prior to the inception of CRT, at the middle (after 12-16 treatments) and at the end (after 24-28 treatments) of the CRT. Descriptive statistics and Mann-Whitney test were computed for fatigue. Gut microbiome data were analyzed using the QIIME2 software.
Participants ( = 29) ranged in age from 37 to 80 years. The median fatigue score significantly changed at the end of CRT (median = 23.0) compared with the median score before the initiation of CRT for the total sample (median = 17.0; ≤ 0.05). At the middle of CRT, the alpha diversity (abundance of Operational Taxonomic Units) was lower for fatigued participants (149.30 ± 53.1) than for nonfatigued participants (189.15 ± 44.18, (23) = 2.08, ≤ 0.05). At the middle of CRT, the alpha diversity (abundance of Operational Taxonomic Units) was lower for fatigued participants (149.30 ± 53.1) than for nonfatigued participants (189.15 ± 44.18, , , and were the dominant phyla for fatigued participants, and , , , and were the most abundant genera for fatigued participants.
CRT-associated perturbation of the gut microbiome composition may contribute to fatigue.
本概念验证研究的目的是:(a) 研究直肠癌成年患者在放化疗(CRT)过程中疲劳及肠道微生物群多样性的时间变化;(b) 调查在CRT中期和末期,疲劳与未疲劳参与者之间肠道微生物群多样性是否存在差异;(c) 调查在CRT中期和末期,疲劳与未疲劳参与者之间在门和属水平上粪便微生物群的相对丰度是否存在差异。
在CRT开始前、CRT中期(12 - 16次治疗后)和末期(24 - 28次治疗后)收集粪便样本和症状评分。对疲劳进行描述性统计和Mann - Whitney检验。使用QIIME2软件分析肠道微生物群数据。
参与者(n = 29)年龄在37至80岁之间。与整个样本CRT开始前的中位数评分(中位数 = 17.0)相比,CRT末期的中位数疲劳评分显著变化(中位数 = 23.0;P≤0.05)。在CRT中期,疲劳参与者的α多样性(操作分类单元丰度)(149.30±53.1)低于未疲劳参与者(189.15±44.18,U(23)=2.08,P≤0.05)。在CRT中期,疲劳参与者的α多样性(操作分类单元丰度)(149.30±53.1)低于未疲劳参与者(189.15±44.18),,,和是疲劳参与者的主要门,,,和是疲劳参与者中最丰富的属。
CRT相关的肠道微生物群组成扰动可能导致疲劳。