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http://www.diva-portal.org/smash/record.jsf?pid=diva2:1415500&dswid=9881
Nilsson, Isabell
Palmer, Jeremy
Apostolou, Eirini
Linköping University.
Rizwan, Muhammad
Linköping University.
Gottfries, Carl Gerhard
Rosén, Anders
Linköping University.
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(English)
Abstract [en]
Metabolic profiling studies have recently indicated dysfunctional mitochondria in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). This includes an impaired function of pyruvate dehydrogenase complex (PDC), possibly driven by serum factor(s), which leads to inadequate adenosine triphosphate generation and excessive lactate accumulation. A reminiscent energy blockade is likely to occur in primary biliary cholangitis (PBC), caused by anti-PDC autoantibodies, as recently proposed. PBC is associated with fatigue and post-exertional malaise, also signifying ME/CFS.
We herein have investigated whether ME/CFS patients have autoreactive antibodies that could interfere with mitochondrial function.
We found that only 1 of 161 examined ME/CFS patients was positive for anti-PDC, while all PBC patients (15/15) presented significant IgM, IgG, and IgA anti-PDC reactivity, as previously shown.
None of fibromyalgia patients (0/14), multiple sclerosis patients (0/29), and healthy blood donors (0/44) controls showed reactivities.
Anti-mitochondrial autoantibodies (inner and outer membrane) were negative in ME/CFS cohort.
Anti-cardiolipin antibody levels in patients did not differ significantly from healthy blood donors.
In conclusion, the impaired mitochondrial/metabolic dysfunction, observed in ME/CFS, cannot be explained by presence of circulating autoantibodies against the tested mitochondrial epitopes.
National Category
Medical and Health Sciences
Identifiers
URN: urn:nbn:se:liu:diva-164349DOI: 10.3389/fmed.2020.00108OAI: oaiiVA.org:liu-164349DiVA, id: diva2:1415500
Available from: 2020-03-18 Created: 2020-03-18 Last updated: 2020-03-18