ME/CFS Evidence Browser — Classified Studies on Myalgic Encephalomyelitis

1701–1720 of 6,188 studies

E2 ModerateCohortPEM unclearCross-Sectional

Comparison of the finger plethysmography derived stroke volumes by Nexfin CO Trek and suprasternal aortic Doppler derived stroke volume measurements in adults with myalgic encephalomyelitis/chronic fatigue syndrome and in healthy controls.

van Campen, C Linda M C, Verheugt, Freek W A, Rowe, Peter C et al.·Technology and health care : official journal of the European Society for Engineering and Medicine·2021

This study compared two different ways of measuring how much blood the heart pumps with each beat during a tilt table test (where patients lie down then are tilted upright). Researchers tested 154 ME/CFS patients and 39 healthy people using finger cuff measurements and ultrasound of the heart. They found that the finger cuff method gave higher readings than ultrasound, but after adjusting the finger cuff numbers to match ultrasound values, the device became reliable enough to track changes during tilt testing.

Autonomic Nervous System

E2 ModerateCohortPEM unclearObservational

Beyond bones: The relevance of variants of connective tissue (hypermobility) to fibromyalgia, ME/CFS and controversies surrounding diagnostic classification: an observational study.

Eccles, Jessica A, Thompson, Beth, Themelis, Kristy et al.·Clinical medicine (London, England)·2021

This study looked at whether joint hypermobility (unusual flexibility and loose joints) is connected to fibromyalgia and ME/CFS. Researchers found that most patients with these conditions also had signs of hypermobility, and that higher hypermobility scores matched with worse symptoms. The results suggest that hypermobility is often missed in diagnosis, even though it significantly affects how sick people feel.

Diagnostics

E2 ModerateBehavioralPEM unclearObservational

Effectiveness of Internet-Based Cognitive Behavior Therapy (Fatigue in Teenagers on the Internet) for Adolescents With Chronic Fatigue Syndrome in Routine Clinical Care: Observational Study.

Albers, Eline, Nijhof, Linde N, Berkelbach van der Sprenkel, Emma E et al.·Journal of medical Internet research·2021

This study tested whether an internet-based therapy program called FITNET, delivered through routine clinical care, works as well as it did in earlier controlled research. The program helps teenagers with ME/CFS through structured cognitive behavioral therapy done online. Results showed that teenagers improved significantly with similar outcomes to the original research study, and very few got worse during treatment.

E2 ModerateCohortPEM unclearCross-Sectional

A Comprehensive Examination of Severely Ill ME/CFS Patients.

Chang, Chia-Jung, Hung, Li-Yuan, Kogelnik, Andreas M et al.·Healthcare (Basel, Switzerland)·2021

This study examined severely ill ME/CFS patients who are mostly housebound or bedbound—a group that hasn't received much research attention. Researchers found that fatigue, pain, and thinking difficulties were the most common complaints, and patients showed distinct sleep problems and hormone imbalances. The study suggests that ME/CFS and long COVID may share similar mechanisms, meaning treatments discovered for one condition could potentially help the other.

Long COVID OverlapPost-Exertional Malaise

E2 ModerateCohortPEM requiredCross-Sectional

Hand grip strength and fatigability: correlation with clinical parameters and diagnostic suitability in ME/CFS.

Jäkel, Bianka, Kedor, Claudia, Grabowski, Patricia et al.·Journal of translational medicine·2021

This study tested hand grip strength in ME/CFS patients compared to healthy people and cancer patients to see if it could help diagnose the condition. Researchers found that ME/CFS patients had weaker grip strength and their muscles got tired much faster during repeated squeezing tests. Importantly, their muscles also recovered more slowly after resting for an hour, suggesting that muscle fatigue is a real, measurable feature of ME/CFS.

Post-Exertional Malaise

E2 ModerateCohortPEM requiredCross-Sectional

Post-Acute COVID-19 Symptoms, a Potential Link with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: A 6-Month Survey in a Mexican Cohort.

González-Hermosillo, J Antonio, Martínez-López, Jhanea Patricia, Carrillo-Lampón, Sofía Antonieta et al.·Brain sciences·2021

This study followed 130 people recovering from COVID-19 for 6 months to see how many developed symptoms similar to ME/CFS. Nearly half the patients experienced ongoing fatigue, and those with fatigue tended to be older and had spent more time in the hospital. Only 13% of the patients met the strict diagnostic criteria for ME/CFS, suggesting that while some people have overlapping symptoms, post-COVID fatigue and ME/CFS may be distinct conditions.

E2 ModerateCohortPEM unclearCross-Sectional

A Comparison of Patients with Chronic Fatigue Syndrome and Myalgic Encephalomyelitis from the United States and Japan.

Wiedbusch, Elzbieta, Cotler, Joseph, Jason, Leonard A·Journal of preventive medicine & healthcare·2021

This study compared how ME/CFS affects people in the United States and Japan by surveying 124 Japanese patients and 210 U.S. patients. The research found that U.S. patients reported more severe brain fog, stomach problems, and exhaustion after activity compared to Japanese patients. Interestingly, Japanese women experienced similar levels of disability as American patients despite being less likely to receive official disability support.

Post-Exertional Malaise

E2 ModerateCohortPEM unclearCross-Sectional

The Prevalence of Pediatric Myalgic Encephalomyelitis/Chronic Fatigue Syndrome in a Community‑Based Sample.

Jason, Leonard A, Katz, Ben Z, Sunnquist, Madison et al.·Child & youth care forum·2020

Researchers studied over 10,000 children and teenagers in the Chicago area to find out how many have ME/CFS. They found that about 0.75% (roughly 1 in 133) young people have the condition, with higher rates among African American and Latino youth. Importantly, less than 5% of these children had been diagnosed before the study, meaning many young people with ME/CFS are going unrecognized by doctors.

Diagnostics

E2 ModerateCohortPEM unclearCase-Control

Changes in DNA methylation profiles of myalgic encephalomyelitis/chronic fatigue syndrome patients reflect systemic dysfunctions.

Helliwell, A M, Sweetman, E C, Stockwell, P A et al.·Clinical epigenetics·2020

This study looked at chemical tags on DNA called methylation patterns in people with ME/CFS compared to healthy people. These tags can turn genes on or off without changing the DNA itself. Researchers found that people with ME/CFS have different methylation patterns, particularly in genes related to energy production, immune function, and brain chemistry, which may help explain why they experience the symptoms they do.

Energy MetabolismImmune System

E2 ModerateCohortPEM unclearCross-Sectional

Properties of measurements obtained during cardiopulmonary exercise testing in individuals with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.

Davenport, Todd E, Stevens, Staci R, Stevens, Jared et al.·Work (Reading, Mass.)·2020

Researchers tested whether a standard exercise test (cardiopulmonary exercise test, or CPET) could reliably measure how ME/CFS affects the body's ability to exercise. They had 51 women with ME/CFS and 10 healthy women do the same exercise test twice, 24 hours apart. The results showed that the measurements were consistent and clearly different between the two groups, suggesting that CPET could be a useful tool for assessing ME/CFS.

Biomarkers

E2 ModerateCohortPEM not requiredCross-Sectional

Self-reported cognitive impairment in individuals with Primary Immunodeficiency Disease.

Sowers, Kerri L, Gayda-Chelder, Christine A, Galantino, Mary Lou·Brain, behavior, & immunity - health·2020

This study looked at whether people with Primary Immunodeficiency Disease (PID)—a condition where the immune system doesn't work properly—experience brain fog or memory problems. Researchers asked 292 people with PID to fill out surveys about their memory, mood, and anxiety. They found that people with PID reported significantly more memory problems and higher levels of anxiety and depression compared to people without these conditions.

Cognitive Impairment

E2 ModerateCohortPEM unclearCross-Sectional

Patients with ME/CFS (Myalgic Encephalomyelitis/Chronic Fatigue Syndrome) and chronic pain report similar level of sickness behavior as individuals injected with bacterial endotoxin at peak inflammation.

Jonsjö, Martin A, Åström, Jenny, Jones, Michael P et al.·Brain, behavior, & immunity - health·2020

This study compared how 'sick' people with ME/CFS and chronic pain feel compared to other groups. Researchers found that ME/CFS and chronic pain patients reported feeling as sick as healthy people who were given a bacterial toxin to trigger temporary inflammation. These high levels of sickness feelings were similar across both conditions and higher than what primary care patients reported, suggesting that the persistent sickness sensation in ME/CFS and chronic pain may involve similar biological mechanisms related to inflammation and how the brain processes illness signals.

Immune System

E2 ModerateCohortPEM not requiredCross-Sectional

Functional gastrointestinal disorders are increased in joint hypermobility-related disorders with concomitant postural orthostatic tachycardia syndrome.

Tai, Foong Way David, Palsson, Olafur S, Lam, Ching Y et al.·Neurogastroenterology and motility·2020

This study looked at people with joint hypermobility disorders (including Ehlers-Danlos syndrome) to understand how often they experience stomach and digestive problems. The researchers found that those who also have POTS (a condition affecting heart rate and blood pressure when standing) had significantly more digestive issues than those without POTS. The digestive problems remained worse in the POTS group even after accounting for other conditions like chronic fatigue syndrome.

Autonomic Nervous System

E2 ModerateBehavioralPEM unclearCross-Sectional

Prevalence and treatment of Chronic Fatigue Syndrome/Myalgic Encephalomyelitis and co-morbid severe health anxiety.

Daniels, Jo, Parker, Hannah, Salkovskis, Paul Martin·International journal of clinical and health psychology : IJCHP·2020

This study found that about 42% of people with ME/CFS also experience significant health anxiety—excessive worry about their health and symptoms. When people have both ME/CFS and health anxiety together, they tend to report worse fatigue and more difficulty with physical activities. The researchers tested whether cognitive behavioral therapy (a type of talking therapy) could help reduce health anxiety in ME/CFS patients, and found it produced meaningful improvements.

E2 ModerateCohortPEM unclearCross-Sectional

Deep phenotyping of myalgic encephalomyelitis/chronic fatigue syndrome in Japanese population.

Kitami, Toshimori, Fukuda, Sanae, Kato, Tamotsu et al.·Scientific reports·2020

Researchers studied 48 ME/CFS patients and 52 healthy people in Japan to find biological markers of the disease. They tested blood samples, gut bacteria, immune cells, and sleep patterns, identifying 26 potential markers that differ between patients and healthy people. Three markers stood out as most important: certain types of white blood cells, gut bacteria composition, and fat-like molecules in the blood, which were especially linked to sleep problems in ME/CFS patients.

Energy MetabolismImmune System

E2 ModerateBehavioralPEM unclearLongitudinal

Longitudinal outcomes associated with significant other responses to chronic fatigue and pain.

Schmaling, Karen B, Fales, Jessica L, McPherson, Sterling·Journal of health psychology·2020

This study followed 68 people with chronic fatigue (some also with fibromyalgia) for 18 months to see how their loved ones' responses affected their health outcomes. The researchers found that when significant others responded negatively to fatigue and pain, patients experienced more pain, worse mental health, and worse fatigue symptoms over time. Interestingly, when loved ones were more helpful and comforting (solicitous), patients with more fibromyalgia tender points tended to have this response, and when loved ones helped distract patients, mental health was better.

Pain and Sensitization

E2 ModerateCohortPEM not requiredCross-Sectional

A Cross-National Comparison of Myalgic Encephalomyelitis and Chronic Fatigue Syndrome at Tertiary Care Settings from the US and Spain.

Bhatia, Shaun, Olczyk, Nicole, Jason, Leonard A et al.·American journal of social sciences and humanities·2020

This study compared ME/CFS patients in the United States and Spain to see if the disease affects people differently depending on where they live. Researchers found that Spanish patients reported worse overall health and more severe symptoms, particularly pain and hormone-related problems, compared to American patients. The differences may be due to how each country handles disability benefits, how doctors view ME/CFS, and how easily patients can see specialists.

E2 ModerateMechanismPEM requiredMechanistic

Unravelling myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS): Gender-specific changes in the microRNA expression profiling in ME/CFS.

Cheema, Amanpreet K, Sarria, Leonor, Bekheit, Mina et al.·Journal of cellular and molecular medicine·2020

This study looked at tiny molecules called microRNAs in the blood of people with ME/CFS to understand how their immune system responds to exercise. The researchers discovered that men and women with ME/CFS show different patterns in these molecules, and they also found that nutritional status affects these patterns. These findings could help explain why some people experience worsening symptoms after exercise (post-exertional malaise) and suggest that treatment approaches may need to differ between men and women.

Immune SystemPost-Exertional Malaise

E2 ModerateCohortPEM not requiredCross-Sectional

Hemodynamics during the 10-minute NASA Lean Test: evidence of circulatory decompensation in a subset of ME/CFS patients.

Lee, Jihyun, Vernon, Suzanne D, Jeys, Patricia et al.·Journal of translational medicine·2020

This study tested a simple 10-minute standing test called the NASA Lean Test in ME/CFS patients to understand heart and blood vessel problems that cause dizziness and weakness. Researchers found that patients who became sick more recently (within 4 years) showed signs of circulation problems during the test—their hearts beat faster and their blood pressure changed abnormally—while those sick for over 10 years showed fewer of these changes. The NASA Lean Test appears to be a useful tool that doctors can use to diagnose and monitor these circulation problems.

Autonomic Nervous System

E2 ModerateBehavioralPEM not requiredObservational

Cognitive behavioural therapy for chronic fatigue and chronic fatigue syndrome: outcomes from a specialist clinic in the UK.

Adamson, James, Ali, Sheila, Santhouse, Alastair et al.·Journal of the Royal Society of Medicine·2020

This study looked at whether cognitive behavioural therapy (CBT)—a type of talk therapy focused on changing thoughts and behaviors—helps people with ME/CFS feel better in a real-world clinic setting. Researchers tracked nearly 1,000 patients receiving CBT and found that most improved in fatigue, physical functioning, and social life, with 85% reporting they felt better and 90% satisfied with treatment.

Interventions

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Evidence browser

Comparison of the finger plethysmography derived stroke volumes by Nexfin CO Trek and suprasternal aortic Doppler derived stroke volume measurements in adults with myalgic encephalomyelitis/chronic fatigue syndrome and in healthy controls.

Beyond bones: The relevance of variants of connective tissue (hypermobility) to fibromyalgia, ME/CFS and controversies surrounding diagnostic classification: an observational study.

Effectiveness of Internet-Based Cognitive Behavior Therapy (Fatigue in Teenagers on the Internet) for Adolescents With Chronic Fatigue Syndrome in Routine Clinical Care: Observational Study.

A Comprehensive Examination of Severely Ill ME/CFS Patients.

Hand grip strength and fatigability: correlation with clinical parameters and diagnostic suitability in ME/CFS.

Post-Acute COVID-19 Symptoms, a Potential Link with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: A 6-Month Survey in a Mexican Cohort.

A Comparison of Patients with Chronic Fatigue Syndrome and Myalgic Encephalomyelitis from the United States and Japan.

The Prevalence of Pediatric Myalgic Encephalomyelitis/Chronic Fatigue Syndrome in a Community‑Based Sample.

Changes in DNA methylation profiles of myalgic encephalomyelitis/chronic fatigue syndrome patients reflect systemic dysfunctions.

Properties of measurements obtained during cardiopulmonary exercise testing in individuals with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.

Self-reported cognitive impairment in individuals with Primary Immunodeficiency Disease.

Patients with ME/CFS (Myalgic Encephalomyelitis/Chronic Fatigue Syndrome) and chronic pain report similar level of sickness behavior as individuals injected with bacterial endotoxin at peak inflammation.

Functional gastrointestinal disorders are increased in joint hypermobility-related disorders with concomitant postural orthostatic tachycardia syndrome.

Prevalence and treatment of Chronic Fatigue Syndrome/Myalgic Encephalomyelitis and co-morbid severe health anxiety.

Deep phenotyping of myalgic encephalomyelitis/chronic fatigue syndrome in Japanese population.

Longitudinal outcomes associated with significant other responses to chronic fatigue and pain.

A Cross-National Comparison of Myalgic Encephalomyelitis and Chronic Fatigue Syndrome at Tertiary Care Settings from the US and Spain.

Unravelling myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS): Gender-specific changes in the microRNA expression profiling in ME/CFS.

Hemodynamics during the 10-minute NASA Lean Test: evidence of circulatory decompensation in a subset of ME/CFS patients.

Cognitive behavioural therapy for chronic fatigue and chronic fatigue syndrome: outcomes from a specialist clinic in the UK.

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