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DOI 10.1038/s41598-018-20941-w

Медицинская библиотека · Scientific reports · 2018

Value of Circulating Cytokine Profiling During Submaximal Exercise Testing in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.

Moneghetti Kegan J, Skhiri Mehdi, Contrepois Kévin, Kobayashi Yukari, Maecker Holden, Davis Mark, Snyder Michael, Haddad Francois, Montoya Jose G

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Myalgic Encephalomyelitis or Chronic Fatigue Syndrome (ME/CFS) is a heterogeneous syndrome in which patients often experience severe fatigue and malaise following exertion. Immune and cardiovascular dysfunction have been postulated to play a role in the pathophysiology. We therefore, examined whether cytokine profiling or cardiovascular testing following exercise would differentiate patients with ME/CFS. Twenty-four ME/CFS patients were matched to 24 sedentary controls and underwent cardiovascular and circulating immune profiling. Cardiovascular analysis included echocardiography, cardiopulmonary exercise and endothelial function testing. Cytokine and growth factor profiles were analyzed using a 51-plex Luminex bead kit at baseline and 18 hours following exercise. Cardiac structure and exercise capacity were similar between groups. Sparse partial least square discriminant analyses of cytokine profiles 18 hours post exercise offered the most reliable discrimination between ME/CFS and controls (κ = 0.62(0.34,0.84)). The most discriminatory cytokines post exercise were CD40L, platelet activator inhibitor, interleukin 1-β, interferon-α and CXCL1. In conclusion, cytokine profiling following exercise may help differentiate patients with ME/CFS from sedentary controls.

Для цитирования: Moneghetti Kegan J, Skhiri Mehdi, Contrepois Kévin, Kobayashi Yukari, Maecker Holden, Davis Mark, Snyder Michael, Haddad Francois, Montoya Jose G. Value of Circulating Cytokine Profiling During Submaximal Exercise Testing in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.. Scientific reports. 2018. DOI: 10.1038/s41598-018-20941-w.

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