Department of Psychiatry and Addiction, Telemark Hospital Trust, Skien, Norway.
Department of Oncology and Medical Physics, Haukeland University Hospital, Bergen, Norway.
PLoS One. 2023 Feb 2;18(2):e0280942. doi: 10.1371/journal.pone.0280942. eCollection 2023.
A few earlier studies have found impaired endothelial function in patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS). The present study investigated large-vessel and small-vessel endothelial function in patients with ME/CFS.
The study was a substudy of the RituxME trial, a national, multicenter, randomized, double-blind, placebo-controlled phase III study on the effect of rituximab vs. placebo in ME/CFS patients in Norway. Flow-mediated dilation (FMD) and post-occlusive reactive hyperemia (PORH) was measured at baseline and after 18 months of treatment in 39 patients and compared with healthy controls. Other outcome measures were symptom severity and various physical function measures.
ME/CFS patients had markedly reduced FMD compared to healthy controls at baseline (5.1% vs. 8.2%, p< 0.0001, adjusted for arterial diameter and sex), and significantly lower microvascular regulation measured by PORH than healthy controls (1354 PU vs. 2208 PU, p = 0.002). There were no differences between the treatment and placebo groups in symptom changes or vascular measures. As a group, the ME/CSF patients experienced a slight, but significant improvement in clinical symptoms after 18 months. PORH, but not FMD, was similarly improved (1360 to 1834 PU, p = 0.028). There was no significant correlation between FMD and PORH. There were non-significant tendencies towards associations between symptom severity/physical function measures and lower FMD and PORH, and a significant correlation between PORH and steps per 24 hours at baseline.
ME/CFS patients had reduced macro- and microvascular endothelial function, indicating that vascular homeostasis may play a role in the clinical presentation of this disease.
一些早期研究发现,肌痛性脑脊髓炎/慢性疲劳综合征(ME/CFS)患者的内皮功能受损。本研究旨在探讨 ME/CFS 患者的大血管和小血管内皮功能。
该研究是 RituxME 试验的子研究,RituxME 试验是一项在挪威进行的全国性、多中心、随机、双盲、安慰剂对照的 III 期研究,旨在评估利妥昔单抗与安慰剂对 ME/CFS 患者的疗效。在基线时和治疗 18 个月后,对 39 例患者进行血流介导的扩张(FMD)和闭塞后反应性充血(PORH)测量,并与健康对照组进行比较。其他结果测量包括症状严重程度和各种身体功能测量。
与健康对照组相比,ME/CFS 患者在基线时的 FMD 明显降低(5.1%对 8.2%,p<0.0001,调整动脉直径和性别),PORH 测量的微血管调节也明显低于健康对照组(1354 PU 对 2208 PU,p=0.002)。治疗组和安慰剂组在症状变化或血管测量方面均无差异。作为一个整体,ME/CSF 患者在 18 个月后经历了轻微但显著的临床症状改善。PORH 而非 FMD 也得到了类似的改善(1360 对 1834 PU,p=0.028)。FMD 和 PORH 之间无显著相关性。FMD 和 PORH 较低与症状严重程度/身体功能测量呈显著负相关,而 PORH 与基线时的 24 小时步数呈显著正相关。
ME/CFS 患者的大血管和小血管内皮功能降低,表明血管稳态可能在该疾病的临床表现中发挥作用。