Meester Irene, Rivera-Silva Gerardo Francisco, González-Salazar Francisco
Laboratory of Tissue Engineering and Regenerative Medicine, Basic Sciences Department, University of Monterrey, San Pedro Garza García, Mexico.
Laboratory of Cellular Physiology, Northeast Center of Research, Mexican Institute of Social Security, Monterrey, Mexico.
Front Neurosci. 2020 Jan 17;13:1414. doi: 10.3389/fnins.2019.01414. eCollection 2019.
The fibromyalgia syndrome (FMS) is characterized by chronic widespread pain, sleep disturbances, fatigue, and cognitive alterations. A limited efficacy of targeted treatment and a high FMS prevalence (2-5% of the adult population) sums up to high morbidity. Although, altered nociception has been explained with the central sensitization hypothesis, which may occur after neuropathy, its molecular mechanism is not understood. The marked female predominance among FMS patients is often attributed to a psychosocial predisposition of the female gender, but here we will focus on sex differences in neurobiological processes, specifically those of the immune system, as various immunological biomarkers are altered in FMS. The activation of innate immune sensors is compatible with a neuropathy or virus-induced autoimmune diseases. Considering sex differences in the immune system and the clustering of FMS with autoimmune diseases, we hypothesize that the female predominance in FMS is due to a neuropathy-induced autoimmune pathophysiology. We invite the scientific community to verify the autoimmune hypothesis for FMS.
纤维肌痛综合征(FMS)的特征是慢性广泛性疼痛、睡眠障碍、疲劳和认知改变。靶向治疗效果有限且FMS患病率高(占成年人口的2%-5%),这些因素导致了高发病率。虽然伤害感受的改变已用中枢敏化假说来解释,这种情况可能在神经病变后发生,但其分子机制尚不清楚。FMS患者中女性明显居多,这通常归因于女性的心理社会易感性,但在此我们将关注神经生物学过程中的性别差异,特别是免疫系统的差异,因为FMS中各种免疫生物标志物都发生了改变。先天免疫传感器的激活与神经病变或病毒诱导的自身免疫性疾病相符。考虑到免疫系统中的性别差异以及FMS与自身免疫性疾病的聚集现象,我们假设FMS中女性居多是由于神经病变诱导的自身免疫病理生理学所致。我们邀请科学界验证FMS的自身免疫假说。