Brain Health Clinic UK

Brain Health Clinic UK Specialist Neuropsychiatry Clinic for Adult ADHD, Autism, FND, Dementia, Psychosis, Bipolar, Depression, Anxiety

Post-Viral Fatigue SyndromeMyalgia and joint pain, cognitive deficits, unrefreshing sleep, autonomic dysfunction, neurop...
19/06/2025

Post-Viral Fatigue Syndrome

Myalgia and joint pain, cognitive deficits, unrefreshing sleep, autonomic dysfunction, neuropsychiatric symptoms, and incapacitating post-exertional exhaustion are all
hallmarks of post-viral fatigue syndrome (PVFS), a broad category of complicated neuroimmune illnesses with unclear aetiology. It encompasses fibromyalgia (FM), myalgia encephalomyelitis, sometimes referred to as chronic fatigue syndrome (ME/CFS), and, more recently, the COVID-19 illness (long COVID).

The hallmark symptom of PVFS is prolonged post-exertional fatigue, which gets worse with little physical or mental effort.

Other symptoms include joint and myalgia pain, cognitive impairments, unrefreshing sleep, dysautonomia, and neuropsychiatric symptoms like apathy, anxiety/depression, and emotional lability, which usually follow recurrent viral infections.

Despite not being a widely recognized ailment, PVFS has
recently been linked more and more to the post-COVID-19 syndrome.

The CDC currently projects that more than 150 million individuals globally will be impacted by a significant rise in ME/CFS
prevalence following COVID-19 by 2050.

Disease onset is multifactorial (i.e., a mix of environmental and immunogenetic elements); it can happen abruptly or evolve gradually over time; and it is usually linked to triggering events, which can include physical and psychological trauma in addition to viral infections. PVFS is often triggered by common viral infections such as the Epstein–Barr virus (EBV), human herpesvirus (HHVs), cytomegalovirus (CMV), SARS-
CoV-2 (COVID-19), amongst others.

Overwhelming exhaustion and extensive physical pain that is not relieved by rest and cannot be attributed to any underlying medical illness are hallmarks of ME/CFS, FM, and long-term COVID, devastating multisystem conditions that affect most body
systems. People may have a variety of symptoms in addition to the "prime" ones of exhaustion and chronic pain, including post-exertional malaise, restless sleep, cognitive deficits known as "brain fog" orthostatic intolerance, and gastrointestinal issues.

Because of their vital function in cellular energy metabolism, mitochondria—the cellular powerhouses that produce energy—have recently attracted attention in PVFS research.

Low-grade systemic inflammation in ME/CFS, FM, and long-term COVID patients has been linked to mitochondrial dysfunction, which includes oxidative stress, redox imbalance, altered mitochondrial membrane potential/permeability, disturbed calcium homeostasis, and impaired ATP production, according to the growing body of research.

Several overlapping symptoms, including cognitive impairments, sleep disruptions, brain fog, concentration/memory deficits, and muscle soreness, are often present in addition to exhaustion in these disorders. At least some of these symptoms can be linked to mitochondrial dysfunction, which can affect how energy is metabolized in the brain.

In both adults and children/adolescents, fibromyalgia patients have decreased tissue levels of CoQ10 (usually 40–50% of the normal amount), along with elevated levels of oxidative stress, inflammation, and mitochondrial dysfunction.

Recent research indicates that, considering the critical role that CoQ10 plays in normal mitochondrial activity, CoQ10 supplementation may play a part in the treatment of the
illnesses.

Through its capacity to restore electron flow in the mitochondrial respiratory chain (MRC), which will increase ATP synthesis by oxidative phosphorylation, CoQ10 supplementation may improve mitochondrial dysfunction and reduce tiredness linked to
PVFS.

Additional randomized controlled trials are needed to demonstrate the effectiveness of CoQ10 supplementation in individuals with ME/CFS and extended COVID. Randomized
controlled clinical trials have reported considerable symptomatic advantages in the treatment of these illnesses, especially for FM.

Notably, clinical trials using CoQ10 supplements in individuals with PVFS and a variety of other chronic conditions have not
revealed any significant negative effects.

Low-grade systemic inflammation in ME/CFS, FM, and long-term COVID has been linked to mitochondrial dysfunction, according
to the growing body of research.

Emerging evidence, including RCTs, supports the efficacy of coenzyme Q10 supplementation on chronic tiredness and pain symptoms as a unique therapeutic approach for the treatment of PVFS.

If you want to speak to a Professional, please visit the website & book an appointment at Brain Health Clinic as Neuropsychiatry Online Clinic.
Please visit www.thebrainhealth.co.uk or write to admin@thebrainhealth.co.uk
0207 183 1229
0756 338 9300

References:
1) Mantle D, Hargreaves IP, Domingo JC, Castro-Marrero J. Mitochondrial Dysfunction and Coenzyme Q10 Supplementation in Post-Viral Fatigue Syndrome: An Overview. Int J Mol Sci. 2024 Jan 1;25(1):574. doi: 10.3390/ijms25010574. PMID: 38203745; PMCID: PMC10779395.
2) Komaroff A.L., Lipkin W.I. ME/CFS and Long COVID share similar symptoms and biological abnormalities: Road map to the literature. Front. Med. 2023;10:1187163. doi: 10.3389/fmed.2023.1187163

3) Komaroff A.L. Chronic “post-infectious” fatigue syndrome. Trans. Am. Acad. Insur. Med. 1993;76:82–95
4) Poenaru S., Abdallah S.J., Corrales-Medina V., Cowan J. COVID-19 and post-infectious myalgic encephalomyelitis/chronic fatigue syndrome: A narrative review. Ther. Adv. Infect. Dis. 2021;8:20499361211009385. doi:10.1177/20499361211009385.
5) Hamilton W.T., Gallagher A.M., Thomas J.M., White P.D. The prognosis of different fatigue diagnostic labels: A longitudinal survey. Fam. Pract. 2005;22:383–388. doi:
10.1093/fampra/cmi021
6) Mahroum N., Shoenfeld Y. Autoimmune Autonomic Dysfunction Syndromes: Potential Involvement and Pathophysiology Related to Complex Regional Pain
Syndrome, Fibromyalgia, Chronic Fatigue Syndrome, Silicone Breast Implant- Related Symptoms and Post-COVID Syndrome. Pathophysiology. 2022;29:414–425. doi: 10.3390/pathophysiology29030033
7) Komaroff A.L., Bateman L. Will COVID-19 Lead to Myalgic
Encephalomyelitis/Chronic Fatigue Syndrome? Front. Med. 2020;7:606824. doi: 10.3389/fmed.2020.606824
8) Komaroff A.L., Lipkin W.I. Insights from myalgic encephalomyelitis/chronic fatigue syndrome may help unravel the pathogenesis of postacute COVID-19 syndrome. Trends Mol. Med. 2021;27:895–906. doi: 10.1016/j.molmed.2021.06.002.
9) Pintos-Pascual I., Moreno-Torres V., Ibanez-Estellez F., Corrales-Rodriguez P., Trevino A., Corpas M., Corral O., Soriano V., de Mendoza C. Is SARS-CoV-2 the only cause of long-COVID? AIDS Rev. 2022;24:183–196. doi: 10.24875/AIDSRev.22000025
10) Thapaliya K., Marshall-Gradisnik S., Barth M., Eaton-Fitch N., Barnden L. Brainstem volume changes in myalgic encephalomyelitis/chronic fatigue syndrome and long COVID patients. Front. Neurosci. 2023;17:1125208. doi:
10.3389/fnins.2023.1125208.
11) Cordero M.D., Diaz-Parrado E., Carrion A.M., Alfonsi S., Sanchez-Alcazar J.A., Bullon P., Battino M., de Miguel M. Is inflammation a mitochondrial dysfunction- dependent event in fibromyalgia? Antioxid. Redox Signal. 2013;18:800–807. doi:
10.1089/ars.2012.4892.

12) Hargreaves I.P. Coenzyme Q10 as a therapy for mitochondrial disease. Int. J. Biochem. Cell Biol. 2014;49:105–111. doi: 10.1016/j.biocel.2014.01.020
13) Mantle D., Hargreaves I.P. Mitochondrial Dysfunction and Neurodegenerative Disorders: Role of Nutritional
Supplementation. Int. J. Mol. Sci. 2022;23:12603.
doi: 10.3390/ijms232012603.
14) Mantle D., Heaton R.A., Hargreaves I.P. Coenzyme Q10 and Immune Function: An Overview. Antioxidants. 2021;10:759. doi: 10.3390/antiox10050759

Fibromyalgia Facts:With a prevalence of 2-3% worldwide, fibromyalgia is a reasonably prevalent syndrome in the general c...
16/06/2025

Fibromyalgia Facts:
With a prevalence of 2-3% worldwide, fibromyalgia is a reasonably prevalent syndrome in the general community.

The diagnosis of fibromyalgia is difficult because of its subjective symptoms, absence of certain biomarkers, and comorbidity with other illnesses. This makes diagnosis difficult and increases the
risk of misdiagnosis, over-diagnosis, and under-diagnosis.

Although the 2016 ACR criteria provide some direction, they still
depend on clinical judgment and might not fully account for the range of conditions.

Fibromyalgia's complicated poly-symptomatology includes somatic symptoms, autonomic problems, cognitive dysfunction, hypersensitivity to external stimuli, psychiatric illnesses, and chronic widespread pain, fatigue, and sleep disruptions.

Early diagnosis and prevention are still unattainable objectives since diagnosis is very clinical and diagnostic criteria are always changing due to the subjectivity of the symptoms and the absence of biomarkers.

Numerous composite tests can be used to assess the severity of fibromyalgia as well as its development or improvement.

Although the exact cause of fibromyalgia is unknown, theories suggest that a combination of genetic predisposition, stressful life events, peripheral (inflammatory), and central (cognitive–emotional) factors lead to pain dys-perception due to
neuro-morphological changes (also known as "nociplastic pain").

Multi-disciplinary treatment should include patient education, brain-retraining, medication, and psychotherapy. The treatment plan should be multimodal, symptom based, and step-by-step, with the patient and the provider identifying common goals.

In short, Chronic widespread pain, hyperalgesia, anxiety, mood disorders, and irregular sleep patterns are among the clinical characteristics of Fibromyalgia. Increased pain sensitivity is the result of changes in several ascending and descending central nervous system pathways as well as peripheral pathways in the pathogenesis and pathophysiology of fibromyalgia. Numerous studies have been conducted on risk factors; the most recent ones concentrate on the roles played by stress, sleep deprivation, and different genetic variables. Finally, pharmacological treatments for fibromyalgia include anti-epileptic medications, tricyclic antidepressants, selective
serotonin reuptake inhibitors (SSRIs), norepinephrine / serotonin reuptake inhibitors (SNRIs), and some experimental medications.

There is growing evidence in favor of non-pharmacologic
therapies like acupuncture, massage therapy, and exercise.

Contact us: Brain Health Clinic
admin@thebrainhealth.co.uk
0207 183 1229 / 0756 338 9300
https://www.thebrainhealth.co.uk/book-online-1

References:
1) https://pmc.ncbi.nlm.nih.gov/articles/PMC7230253/
2) Häuser W, Sarzi-Puttini P, Fitzcharles MA. Fibromyalgia syndrome: under-, over and misdiagnosis. Clin Exp Rheumatol. 2019 Jan-Feb;37 Suppl 116(1):90-97. Epub 2019 Feb 8. PMID: 30747096.
3) Srinivasan S, Maloney E, Wright B, Kennedy M, Kallail KJ, Rasker JJ, Häuser W, Wolfe F. The Problematic Nature of Fibromyalgia Diagnosis in the Community. ACR Open Rheumatol. 2019 Mar 15;1(1):43-51. doi: 10.1002/acr2.1006. PMID:
31777779; PMCID: PMC6857982
4) Sarzi-Puttini, P., Giorgi, V., Marotto, D. et al. Fibromyalgia: an update on clinical characteristics, aetiopathogenesis and treatment. Nat Rev Rheumatol 16, 645–660 (2020). https://doi.org/10.1038/s41584-020-00506-w
5) Chinn, S., Caldwell, W. & Gritsenko, K. Fibromyalgia Pathogenesis and Treatment Options Update. Curr Pain Headache Rep 20, 25 (2016).
https://doi.org/10.1007/s11916-016-0556-x

Dr. Bhuwan Roy, MBBS, MRCPsychGMC Number: 6059986, On GMC Specialist Register since October 2013; Member of the Royal Co...
09/06/2025

Dr. Bhuwan Roy, MBBS, MRCPsych
GMC Number: 6059986, On GMC Specialist Register since October 2013; Member of the Royal College of Psychiatrists, number: 815650

Dr. Bhuwan Roy privately practices at the Brain Health Clinic
( www.thebrainhealth.co.uk ) is a highly experienced Consultant Psychiatrist and Associate Clinical Director at Oxleas NHS Foundation Trust. With over 20 years of experience in psychiatry, Dr. Roy has developed advanced skills in assessing and treating neuropsychiatric illnesses.

Current Role:
As Associate Clinical Director of the Greenwich Acute and Crisis Service Line, Dr. Roy provides clinical and managerial leadership to teams in the directorate, including inpatient wards, crisis and home treatment teams, and liaison services.

Specialties:
Dr. Roy has experience in various psychiatric specialties, including: Psychiatric Intensive Care; Adult ADHD; General Adult Psychiatry; Forensic Psychiatry; Old Age Psychiatry; Liaison Psychiatry; Psychiatry of Learning Disabilities; Substance Misuse Psychiatry.

Therapeutic Experience:
Dr. Roy has received training in Cognitive Analytical Therapy and has experience working with Dialectical Behavioural Therapy models. He has also achieved basic competencies in
psychological therapies.

Leadership and Management:
Dr. Roy has held various leadership roles, including:
Foundation Lead for Kent and Medway NHS and Social Care Partnership Trust
Member of Clinical Governance teams in multiple organizations
Experience managing teams in transition and developing leadership skills

Family-Centered Practice:
Dr. Roy runs a weekly Family/Carers clinic, providing updates on patient care and offering psychoeducational activities.

Other Achievements:
Planned and set up the Abstinence Based Prescribing Clinic
Developed the Beresford Project Opioid Detoxification Pathway treatment protocol
Trained in Neuro-Linguistic Programming to enhance personal development, team working, and leadership skills

Dr. Roy's extensive experience and skills make him a valuable asset to Oxleas NHS Foundation Trust and the psychiatric community.

To book an appointment please contact at admin@thebrainhealth.co.uk or call 0207 183 1229 / 0756 338 9300

https://www.thebrainhealth.co.uk/book-online-1

Address

85 Wimpole Street
London

Opening Hours

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Tuesday 8am - 8pm
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Thursday 8am - 8pm
Friday 8am - 8pm
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Sunday 8am - 8pm

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+442071831229

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