ME/CFS Evidence Browser — Classified Studies on Myalgic Encephalomyelitis

643 studies

281–300 of 643 studies

E0 ConsensusReviewPEM unclearReview-Narrative

Environmental, Neuro-immune, and Neuro-oxidative Stress Interactions in Chronic Fatigue Syndrome.

Bjørklund, Geir, Dadar, Maryam, Pivina, Lyudmila et al.·Molecular neurobiology·2020

This review looked at how ME/CFS develops by examining immune system problems, oxidative stress (cellular damage from harmful molecules), infections, and nutritional issues. Researchers found that people with ME/CFS often have changes in their immune cells and proteins, along with signs of cellular damage that could explain fatigue, pain, and other symptoms. The study suggests that treatments targeting oxidative stress and nutrition might help, though more research is needed.

Immune SystemPost-Exertional Malaise

E0 ConsensusReviewPEM requiredSystematic-Review

Review of case definitions for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS).

Lim, Eun-Jin, Son, Chang-Gue·Journal of translational medicine·2020

This study reviewed how ME/CFS has been defined and diagnosed over the past 34 years, examining 25 different case definitions created by researchers. The researchers found that these definitions fall into four main categories and emphasize different key symptoms—some focus on a viral cause, others on inflammation, and some on multiple system problems. Understanding these different approaches helps doctors and patients recognize that ME/CFS is complex and may require more than one way to diagnose it.

Cognitive ImpairmentPost-Exertional Malaise

E0 ConsensusReviewPEM unclearSystematic-Review

Systematic Review of Primary Outcome Measurements for Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (CFS/ME) in Randomized Controlled Trials.

Kim, Do-Young, Lee, Jin-Seok, Son, Chang-Gue·Journal of clinical medicine·2020

This study examined how researchers measure treatment effects in ME/CFS clinical trials by reviewing 52 studies published between 1996 and 2020. The researchers found that most trials rely on patient questionnaires asking about fatigue, physical function, and quality of life rather than objective blood tests or physical measurements. Three questionnaires—the SF-36, Checklist Individual Strength, and Chalder Fatigue Questionnaire—were used most often to track whether treatments worked.

E0 ConsensusReviewPEM not requiredReview-Narrative

Food Implications in Central Sensitization Syndromes.

Aguilar-Aguilar, Elena, Marcos-Pasero, Helena, Ikonomopoulou, Maria P et al.·Journal of clinical medicine·2020

This review examined what is known about how food affects three related conditions—fibromyalgia, ME/CFS, and multiple chemical sensitivities—that all involve heightened nervous system sensitivity. The authors found that changing diet can help improve quality of life for many patients, but the best approach is personalized and done with help from a dietitian and doctor. They warn against following strict diets without professional guidance.

E0 ConsensusReviewPEM unclearSystematic-Review

A systematic review of metabolomic dysregulation in Chronic Fatigue Syndrome/Myalgic Encephalomyelitis/Systemic Exertion Intolerance Disease (CFS/ME/SEID).

Huth, Teilah Kathryn, Eaton-Fitch, Natalie, Staines, Donald et al.·Journal of translational medicine·2020

Researchers reviewed 11 studies that measured tiny chemical molecules (metabolites) in the blood and urine of ME/CFS patients to see if problems with these chemicals might explain the illness. While they found some patterns—especially with chemicals related to amino acids (building blocks of proteins)—the results were inconsistent across different studies. The researchers concluded that we don't yet have enough evidence that metabolite problems cause ME/CFS.

Biomarkers

E0 ConsensusReviewPEM unclearMeta-Analysis

Elevated Perceived Exertion in People with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome and Fibromyalgia: A Meta-analysis.

Barhorst, Ellen E, Andrae, William E, Rayne, Tessa J et al.·Medicine and science in sports and exercise·2020

This study reviewed 37 research papers that measured how hard exercise feels to people with ME/CFS and fibromyalgia compared to healthy people. The researchers found that people with these conditions consistently felt that exercise required significantly more effort, even when their heart rates and physical performance were similar to healthy controls. This difference was large and consistent across most studies, suggesting that something about how the brain perceives effort may be affected in these illnesses.

Post-Exertional Malaise

E0 ConsensusReviewPEM not requiredSystematic-Review

Behavioural modification interventions for medically unexplained symptoms in primary care: systematic reviews and economic evaluation.

Leaviss, Joanna, Davis, Sarah, Ren, Shijie et al.·Health technology assessment (Winchester, England)·2020

This large review looked at whether talking therapies, exercise programs, and relaxation techniques help people with unexplained symptoms that doctors can't find a physical cause for. The researchers found that some treatments—especially cognitive-behavioral therapy and combination therapies—showed modest improvements in pain, tiredness, and mood in the short term, but these benefits often faded over time. However, no single treatment worked well for everyone, and treatments didn't reduce the overall symptom burden.

E0 ConsensusReviewPEM requiredCommentary

Graded exercise therapy does not restore the ability to work in ME/CFS - Rethinking of a Cochrane review.

Vink, Mark, Vink-Niese, Friso·Work (Reading, Mass.)·2020

This study examined whether graded exercise therapy (GET)—a treatment that gradually increases physical activity—actually helps people with ME/CFS return to work. The researchers found that while previous reviews claimed GET improved tiredness, these claims were based on unreliable self-reported outcomes in studies with serious flaws. When looking at objective measures and real-world outcomes, GET did not help people work better and may have harmed at least half of patients.

Post-Exertional Malaise

E0 ConsensusReviewPEM requiredMeta-Analysis

Meta-analysis investigating post-exertional malaise between patients and controls.

Brown, Abigail, Jason, Leonard A·Journal of health psychology·2020

This study looked at research from multiple studies to understand how common post-exertional malaise (PEM) is in people with ME/CFS. Post-exertional malaise is when symptoms get worse after physical or mental activity. The researchers found that people with ME/CFS are about 10 times more likely to experience post-exertional malaise than people without the condition, suggesting it is a key feature of ME/CFS.

Post-Exertional Malaise

E0 ConsensusReviewPEM not requiredSystematic-Review

Advances in Clinical Research on Traditional Chinese Medicine Treatment of Chronic Fatigue Syndrome.

Zhang, Xiaoyan, Wang, Miao, Zhou, Shigao·Evidence-based complementary and alternative medicine : eCAM·2020

This review looked at research on traditional Chinese medicine (TCM) treatments for chronic fatigue syndrome over a five-year period. Researchers found that many clinical studies showed TCM may help improve CFS symptoms, but the results are still not completely clear. The review examined different TCM approaches including syndrome-based treatment, external therapies, and combinations with other treatments.

Interventions

E0 ConsensusReviewPEM not requiredSystematic-Review

Using structural and functional MRI as a neuroimaging technique to investigate chronic fatigue syndrome/myalgic encephalopathy: a systematic review.

Almutairi, Basim, Langley, Christelle, Crawley, Esther et al.·BMJ open·2020

This review examined brain imaging studies in ME/CFS patients using two main techniques: structural MRI (which shows the anatomy of the brain) and functional MRI (which shows which brain areas are active during tasks). Researchers found that ME/CFS patients showed some differences in brain structure and unusual patterns of brain activity, but these findings varied widely between studies. While these results suggest something is happening in the brains of ME/CFS patients, the researchers couldn't identify one clear pattern that all patients share.

E0 ConsensusReviewPEM requiredSystematic-Review

Systematic Review of the Epidemiological Burden of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Across Europe: Current Evidence and EUROMENE Research Recommendations for Epidemiology.

Estévez-López, Fernando, Mudie, Kathleen, Wang-Steverding, Xia et al.·Journal of clinical medicine·2020

This research review looked at how common ME/CFS is across Europe by examining studies published between 1994 and 2019. The researchers found very few good-quality studies on this topic, and the estimates of how many people have ME/CFS varied widely (from 0.1% to 2.2% of the population). The review concludes that we urgently need better, larger studies to understand how many Europeans actually have this condition.

E0 ConsensusReviewPEM unclearSystematic-Review

A relational analysis of an invisible illness: A meta-ethnography of people with chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) and their support needs.

Pilkington, Karen, Ridge, Damien T, Igwesi-Chidobe, Chinonso N et al.·Social science & medicine (1982)·2020

This study examined 47 previous research papers about what people with ME/CFS need in terms of support from family, friends, and healthcare providers. The researchers found that the biggest problems people face come from how others interact with them—including feeling invisible, losing their sense of self, and having difficult experiences at doctor's appointments. The study suggests that focusing on building better relationships and understanding in all areas of life (not just medical treatment) may be key to improving support for people with ME/CFS.

E0 ConsensusReviewPEM unclearSystematic-Review

Management of chronic fatigue syndrome/myalgic encephalomyelitis in a pediatric population: A scoping review.

Collard, Sarah S, Murphy, Jane·Journal of child health care : for professionals working with children in the hospital and community·2020

This review examined research on how to help children and teens with ME/CFS feel better through nutrition, exercise, and psychological support. The researchers found that exercise programs and a combination of treatments (including therapy, exercise, nutrition advice, and family support) helped reduce fatigue and improve school attendance. However, very few studies have looked at ME/CFS in younger children, so more research is needed.

E0 ConsensusReviewPEM unclearSystematic-Review

Assessment of the scientific rigour of randomized controlled trials on the effectiveness of cognitive behavioural therapy and graded exercise therapy for patients with myalgic encephalomyelitis/chronic fatigue syndrome: A systematic review.

Ahmed, S A, Mewes, J C, Vrijhoef, Hjm·Journal of health psychology·2020

This review examined 18 previous studies that tested cognitive behavioural therapy (talk therapy focused on thoughts and behaviors) and graded exercise therapy (gradually increasing physical activity) for ME/CFS. The reviewers found that most of these studies had significant problems in how they were designed and conducted, which means we cannot be confident in their results. The review highlights that better, more carefully designed studies are needed with better ways of measuring improvements.

Interventions

E0 ConsensusReviewPEM unclearSystematic-Review

A systematic review of mitochondrial abnormalities in myalgic encephalomyelitis/chronic fatigue syndrome/systemic exertion intolerance disease.

Holden, Sean, Maksoud, Rebekah, Eaton-Fitch, Natalie et al.·Journal of translational medicine·2020

This review looked at 19 studies examining whether the power-generating structures in our cells (called mitochondria) work differently in people with ME/CFS compared to healthy people. While many studies found some differences in how these cellular power plants function, the results were inconsistent across different research groups, making it hard to draw clear conclusions about whether mitochondrial problems actually cause ME/CFS.

Biomarkers

E0 ConsensusReviewPEM unclearSystematic-Review

A systematic review of neurological impairments in myalgic encephalomyelitis/ chronic fatigue syndrome using neuroimaging techniques.

Maksoud, Rebekah, du Preez, Stanley, Eaton-Fitch, Natalie et al.·PloS one·2020

This review examined 55 studies that used brain imaging techniques to look for physical differences in the brains of people with ME/CFS compared to healthy people. The researchers found evidence that ME/CFS affects how the nervous system works, including changes in brain structure and blood flow. However, the findings weren't consistent across all studies, meaning scientists still don't have a complete picture of what's happening in the brain.

Autonomic Nervous SystemCognitive Impairment

E0 ConsensusReviewPEM unclearMeta-Analysis

Effectiveness of Active Therapy-Based Training to Improve the Balance in Patients with Fibromyalgia: A Systematic Review with Meta-Analysis.

Del-Moral-García, María, Obrero-Gaitán, Esteban, Rodríguez-Almagro, Daniel et al.·Journal of clinical medicine·2020

People with fibromyalgia often have trouble with balance, which increases their risk of falling and affects their ability to do daily activities. This review looked at 10 studies testing whether active exercise-based training programs could help improve balance in fibromyalgia patients. The results showed that these training programs did help people improve their balance and stability compared to other treatments or no treatment.

E0 ConsensusReviewPEM not requiredSystematic-Review

Systematic Review and Meta-analysis of Postlicensure Observational Studies on Human Papillomavirus Vaccination and Autoimmune and Other Rare Adverse Events.

Willame, Corinne, Gadroen, Kartini, Bramer, Wichor et al.·The Pediatric infectious disease journal·2020

Researchers reviewed 22 studies that tracked the safety of HPV vaccines (which prevent certain cancers) in millions of people after the vaccines were approved for use. They looked specifically at whether these vaccines were linked to autoimmune diseases—conditions where the immune system attacks the body. Overall, they found no clear connection between HPV vaccines and most rare diseases, though a few associations (both positive and negative) were noted.

E0 ConsensusReviewPEM not required

The Lonely, Isolating, and Alienating Implications of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.

Boulazreg, Samir, Rokach, Ami·Healthcare (Basel, Switzerland)·2020

This study examines how ME/CFS affects people's emotional and social well-being, focusing particularly on loneliness. The researchers reviewed existing research to understand how ME/CFS creates isolation for patients during their teenage and adult years, and how it also impacts family members and healthcare workers. The study brings together information about loneliness and chronic illness to help explain why ME/CFS can feel so isolating and offers some strategies that might help people cope with these feelings.

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Environmental, Neuro-immune, and Neuro-oxidative Stress Interactions in Chronic Fatigue Syndrome.

Review of case definitions for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS).

Systematic Review of Primary Outcome Measurements for Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (CFS/ME) in Randomized Controlled Trials.

Food Implications in Central Sensitization Syndromes.

A systematic review of metabolomic dysregulation in Chronic Fatigue Syndrome/Myalgic Encephalomyelitis/Systemic Exertion Intolerance Disease (CFS/ME/SEID).

Elevated Perceived Exertion in People with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome and Fibromyalgia: A Meta-analysis.

Behavioural modification interventions for medically unexplained symptoms in primary care: systematic reviews and economic evaluation.

Graded exercise therapy does not restore the ability to work in ME/CFS - Rethinking of a Cochrane review.

Meta-analysis investigating post-exertional malaise between patients and controls.

Advances in Clinical Research on Traditional Chinese Medicine Treatment of Chronic Fatigue Syndrome.

Using structural and functional MRI as a neuroimaging technique to investigate chronic fatigue syndrome/myalgic encephalopathy: a systematic review.

Systematic Review of the Epidemiological Burden of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Across Europe: Current Evidence and EUROMENE Research Recommendations for Epidemiology.

A relational analysis of an invisible illness: A meta-ethnography of people with chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) and their support needs.

Management of chronic fatigue syndrome/myalgic encephalomyelitis in a pediatric population: A scoping review.

Assessment of the scientific rigour of randomized controlled trials on the effectiveness of cognitive behavioural therapy and graded exercise therapy for patients with myalgic encephalomyelitis/chronic fatigue syndrome: A systematic review.

A systematic review of mitochondrial abnormalities in myalgic encephalomyelitis/chronic fatigue syndrome/systemic exertion intolerance disease.

A systematic review of neurological impairments in myalgic encephalomyelitis/ chronic fatigue syndrome using neuroimaging techniques.

Effectiveness of Active Therapy-Based Training to Improve the Balance in Patients with Fibromyalgia: A Systematic Review with Meta-Analysis.

Systematic Review and Meta-analysis of Postlicensure Observational Studies on Human Papillomavirus Vaccination and Autoimmune and Other Rare Adverse Events.

The Lonely, Isolating, and Alienating Implications of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.

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