Gräns Hanna, Nilsson Maria, Dahlman-Wright Karin, Evengård Birgitta
Department of Laboratory Medicine, Division of Clinical Bacteriology, Karolinska Institutet, Karolinska University Hospital, Huddinge, Stockholm, Sweden.
J Clin Pathol. 2007 Feb;60(2):195-8. doi: 10.1136/jcp.2005.035956. Epub 2006 May 26.
Chronic fatigue syndrome (CFS) is an illness with unknown aetiology and pathophysiology. The difference in incidence by sex observed for CFS indicates a role for oestrogen and oestrogen receptors in disease development. Furthermore, an immunomediated pathogenesis has been suggested for CFS, providing an additional connection to oestrogen, which displays immunomodular functions.
To investigate a possible association of oestrogen receptor (ER) mRNAs and two ERbeta single-nucleotide polymorphisms (SNPs) with CFS.
Messenger RNA levels of ERalpha, ERbeta wt and ERbeta cx were investigated in peripheral blood mononuclear cells from 30 patients with CFS and 36 healthy controls by quantitative real-time polymerase chain reaction. Two ERbeta SNPs were scored in the same material.
The CFS group showed significantly lower mRNA expression levels of ERbeta wt compared with the healthy control group. No differences were observed for ERalpha or ERbeta cx between patients and controls. There were no significant differences in frequency for the investigated ERbeta SNPs between cases and controls.
The reduced ERbeta wt expression level observed in this study is consistent with an immune-mediated pathogenesis of CFS. Additionally, the observation that ERbeta wt expression is decreased in CFS could provide an entry point to identify interesting, potentially disease-causing, candidate molecules for further study. A possible connection between oestrogen, oestrogen receptors and CFS should be evaluated further.
慢性疲劳综合征(CFS)是一种病因和病理生理学不明的疾病。CFS在发病率上的性别差异表明雌激素和雌激素受体在疾病发展中起作用。此外,有人提出CFS存在免疫介导的发病机制,这为雌激素提供了另一种联系,因为雌激素具有免疫调节功能。
研究雌激素受体(ER)mRNA和两种雌激素受体β单核苷酸多态性(SNP)与CFS之间可能存在的关联。
采用定量实时聚合酶链反应,对30例CFS患者和36例健康对照者外周血单个核细胞中的ERα、野生型ERβ和截短型ERβ的信使RNA水平进行了研究。在同一批样本中对两种雌激素受体β单核苷酸多态性进行评分。
与健康对照组相比,CFS组野生型ERβ的mRNA表达水平显著降低。患者与对照组之间的ERα或截短型ERβ未观察到差异。病例组和对照组之间所研究的雌激素受体β单核苷酸多态性频率无显著差异。
本研究中观察到的野生型ERβ表达水平降低与CFS的免疫介导发病机制一致。此外,CFS中野生型ERβ表达降低这一观察结果可为识别有趣的、潜在致病的候选分子以供进一步研究提供切入点。雌激素、雌激素受体与CFS之间的可能联系应进一步评估。