Department of Physical Therapy, Occupational Therapy, Rehabilitation and Physical Medicine, Facultad de Ciencias de la Salud, Universidad Rey Juan Carlos, Avenida de Atenas s/n, 28922 Alcorcón, Madrid, Spain.
Breast. 2012 Apr;21(2):199-203. doi: 10.1016/j.breast.2011.09.012. Epub 2011 Oct 5.
Stress can play an important role in development of cancer-related fatigue (CRF) by activating the hypothalamic-pituitary-adrenal (HPA) axis, the sympathetic nervous system (SNS), and altering the immune system. This study examined the influence of catechol-O-methyltransferase (COMT) Val158Met genotypes on salivary markers of HPA axis (cortisol), SNS (α-amylase) and immune (IgA) systems, as well as on CRF in breast cancer survivors (BCS). One-hundred BCS participated. After amplifying Val158Met COMT polymorphisms by polymerase chain reaction, three COMT genotypes were considered: Val/Val, Val/Met, Met/Met. Salivary cortisol, α-amylase activity, salivary flow rate, and IgA concentration were collected from non-stimulated saliva. CRF was assessed with the fatigue subscale of the Profile of Mood State (POMS) questionnaire. We found that BCS carrying Met/Met genotype reported higher cortisol concentration, α-amylase activity and greater CRF than those with Val/Met (P < 0.05) and Val/Val (P < 0.001) genotypes. No differences in salivary flow rate or IgA concentration (P > 0.20) were found. The results suggest that BCS carrying Met/Met genotype exhibit greater dysfunction of the HPA axis and SNS system associated with severe CRF. This study is important because it strives to understand biological factors that predispose some BCS to higher levels of CRF.
压力通过激活下丘脑-垂体-肾上腺 (HPA) 轴、交感神经系统 (SNS) 和改变免疫系统,在癌症相关疲劳 (CRF) 的发展中起着重要作用。本研究探讨了儿茶酚氧位甲基转移酶 (COMT) Val158Met 基因型对乳腺癌幸存者 (BCS) 的 HPA 轴 (皮质醇)、SNS (α-淀粉酶) 和免疫 (IgA) 系统的唾液标志物以及 CRF 的影响。共有 100 名 BCS 参与了研究。通过聚合酶链反应扩增 Val158Met COMT 多态性后,考虑了三种 COMT 基因型:Val/Val、Val/Met、Met/Met。从非刺激唾液中收集唾液皮质醇、α-淀粉酶活性、唾液流速和 IgA 浓度。使用状态特质焦虑问卷 (POMS) 问卷的疲劳分量表评估 CRF。我们发现,携带 Met/Met 基因型的 BCS 报告的皮质醇浓度、α-淀粉酶活性和 CRF 高于 Val/Met (P < 0.05) 和 Val/Val (P < 0.001) 基因型。唾液流速或 IgA 浓度没有差异 (P > 0.20)。结果表明,携带 Met/Met 基因型的 BCS 表现出 HPA 轴和 SNS 系统更大的功能障碍,与严重的 CRF 相关。这项研究很重要,因为它试图了解使一些 BCS 更容易出现更高水平 CRF 的生物学因素。