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A groundbreaking blood test, developed by scientists, promises to accurately diagnose Myalgic Encephalomyelitis (ME), also known as Chronic Fatigue Syndrome (CFS), a condition often misunderstood and misdiagnosed in Kenya and globally.
Scientists have announced the development of what they describe as the world's first accurate blood test for Myalgic Encephalomyelitis (ME), commonly known as Chronic Fatigue Syndrome (CFS). This debilitating illness, characterised by extreme fatigue not alleviated by rest, has historically lacked a definitive diagnostic test, leading to prolonged suffering and misdiagnosis for many patients.
The new test, developed by researchers from the University of East Anglia and Oxford BioDynamics, boasts an accuracy of 96% in identifying ME/CFS. It works by analysing how DNA is folded in blood samples, identifying a unique pattern consistently present in individuals with ME/CFS but absent in healthy individuals.
In Kenya, as in many parts of the world, ME/CFS diagnosis currently relies on symptom evaluation and ruling out other conditions with similar presentations, such as anaemia, thyroid disorders, or depression. This often results in a lengthy diagnostic journey, with patients reporting feelings of being ignored or having their illness dismissed as psychological.
While specific prevalence data for ME/CFS in Kenya is limited, the global estimates suggest a significant burden. Before the COVID-19 pandemic, approximately 0.89% of the world's population, or about 71 million people, were estimated to live with ME/CFS. Post-COVID-19 analyses indicate a dramatic increase, with an estimated 275 million people globally now affected, partly due to the overlap with Long COVID symptoms.
ME/CFS is a complex, multi-system disease. Its hallmark symptom is profound fatigue that does not improve with rest and is worsened by physical or mental exertion, a phenomenon known as post-exertional malaise (PEM). Other common symptoms include unrefreshing sleep, cognitive difficulties often described as 'brain fog,' muscle and joint pain, headaches, and dizziness.
The absence of a clear diagnostic test has made ME/CFS a challenging condition for both patients and healthcare providers. The new blood test offers a potential solution to this long-standing problem, promising earlier and more accurate diagnoses.
Researchers are optimistic that this breakthrough could also pave the way for a similar test to diagnose Long COVID, as many patients with post-COVID syndrome exhibit symptoms consistent with ME/CFS. Studies have indicated that a significant percentage of Long COVID patients meet the diagnostic criteria for ME/CFS.
While the development of this blood test is a significant step, some experts urge caution, emphasising the need for independent validation in further clinical studies before widespread implementation. Clarity on timelines for availability in Kenya, associated costs, and regulatory safeguards will be crucial for its successful integration into the healthcare system.
The global prevalence of ME/CFS is estimated to be between 17 and 24 million people, with some studies suggesting up to 275 million worldwide, particularly with the impact of Long COVID. This highlights the urgent need for increased awareness, research investment, and compassionate care for those affected by this often-misunderstood condition.
What to watch next: The independent validation of this blood test and its potential rollout in different healthcare settings, including Kenya, will be critical. Further research into the underlying causes and effective treatments for ME/CFS and Long COVID remains a priority.