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Presymptomatic plasma biomarkers in autosomal dominant Alzheimers disease: sequence and timing

JNNP - Current Issue Published 13 Oct 2026 Relevancy: 52%

WHAT IS ALREADY KNOWN ON THIS TOPIC The molecular pathology of Alzheimer’s disease develops many years before the onset of symptoms, and multiple plasma biomarkers of Alzheimer’s pathology have been identified. Understanding the timing of biomarker abnormality is important to guide trial design for the timing of interventions to prevent the onset of dementia. WHAT THIS STUDY ADDS Using an autosomal dominant Alzheimer’s disease cohort, we identify multiple plasma biomarkers that distinguish mutation carriers from non-carrier familial controls and characterise the timing of these changes relative to symptom onset. We demonstrate that biomarkers show change many years before symptom onset: markers of abnormal tau phosphorylation more than 20 years prior, followed by markers of reactive astrocytosis and synaptic dysfunction approximately 15 years prior and neurodegenerative markers within 10 years of symptoms. HOW THIS STUDY MIGHT AFFECT RESEARCH, PRACTICE OR POLICY Plasma biomarkers could...

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Molecular timeline of preclinical Alzheimers disease: why Autosomal Dominant Alzheimers Disease (ADAD) matters

JNNP - Current Issue Published 13 Oct 2026 Relevancy: 47%

When the causal mutation is known, the challenge shifts from identifying disease origins to defining its detectable beginning. For decades, the study of Alzheimer’s disease has been framed by a deceptively simple question: when does the disease begin? In autosomal dominant Alzheimer’s disease (ADAD), the causal event is known. Pathogenic variants in amyloid precursor protein (APP) and presenilin 1 (PSEN1) are present from conception, establishing a lifelong predisposition to disease. Yet knowing the cause does not reveal when the disease becomes biologically manifest. The distinction is important: the causal event and the earliest detectable manifestation of disease are not necessarily the same phenomenon. ADAD offers a rare opportunity to investigate the interval between them. Belder et al 1 exploit one of the most informative natural experiments in human neurodegeneration. Unlike sporadic Alzheimer’s disease, where multiple biological processes converge and temporal inference remains challenging, ADAD provides a genetically anchored...

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Physical activity in ALS: friend or foe?

JNNP - Current Issue Published 13 Oct 2026 Relevancy: 30%

The role of physical activity in ALS risk could depend on intensity, sex, genetics, timing and other factors In the paper by Gao et al , a higher level of overall physical activity — whether self-reported or device-measured — was associated with a lower future risk of amyotrophic lateral sclerosis (ALS) in the UK Biobank.1 Interestingly, this protective effect was more pronounced at moderate activity levels and among women and it persisted in people with an increased genetic risk for ALS (ie, individuals homozygous for the C allele at rs12608932 in UNC13A ; a similar trend was observed in C9ORF72 expansion carriers although not statistically significant). There is a long-running concern that high-intensity physical activity may be harmful for ALS. This stems from the long list of elite athletes — particularly those in professional contact sports and high-endurance disciplines — who were diagnosed with and later died from the...

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Beyond Pain Intensity: A Patient-Informed Framework for Documenting Burden in Small Fiber Neuropathy

PubMed - small fiber neuropathy Published 13 Oct 2026 Relevancy: 79%

Small fiber neuropathy (SFN) is a sensory-autonomic neuropathy of thinly myelinated Aδ and unmyelinated C fibers that can produce neuropathic pain and multisystem autonomic symptoms. Although diagnostic criteria and confirmatory testing have improved recognition, SFN burden may remain underrecognized even after diagnosis. This narrative review identifies two complementary documentation failures. The translation problem arises when symptom labels and intensity ratings do not capture effects on...

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The Digital Imperative for Neuro-Otology

PubMed - diagnostic errors AND neurology Published 13 Oct 2026 Relevancy: 65%

This article highlights the growing role of digital medicine in transforming the diagnosis and management of dizziness, vertigo, and other vestibular disorders. Advances such as video-oculography, video head impulse testing, smartphone-based diagnostic tools, and artificial intelligence (AI)-driven clinical decision support systems have created opportunities to deliver expert vestibular care at scale. The authors emphasize that current clinical practice often fails vestibular patients because of...

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Rural Health and Atypical Stroke: Technology-Based Posterior Circulation Stroke Diagnosis

PubMed - diagnostic errors AND neurology Published 13 Oct 2026 Relevancy: 88%

Diagnostic errors cause an estimated 900,000 deaths and disabilities annually in the United States, and stroke is the leading cause of diagnostic error-related harm in US emergency departments. Posterior circulation strokes (PCS's) are frequently misdiagnosed due to atypical presentations such as dizziness. Key contributors to rural-urban care gaps in PCS diagnosis are highlighted for rural care (eg, challenges in bedside diagnosis and limited access to neurologists). Emerging technologies (eg,...

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How well do junior neurology residents recognize multiple sclerosis? Analysis of the "Close the Loop" resident clinical acumen project

PubMed - neurological misdiagnosis Published 13 Oct 2026 Relevancy: 92%

CONCLUSIONS: Acute multiple sclerosis/demyelinating disease presentations pose educational challenges for neurology residents, with errors primarily arising from misclassification of central nervous system etiologies. Diagnostic accuracy was influenced by prior disease history and patient age, highlighting cognitive biases such as framing and anchoring. Structured feedback models like "close the loop" may help improve multiple sclerosis diagnostic acumen in residency training and clinical...

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When dengue is not the answer: diagnostic anchoring bias in febrile illnesses in conflict-affected settings

PubMed - neurological misdiagnosis Published 13 Oct 2026 Relevancy: 61%

Dengue is an increasingly prevalent arboviral infection in tropical regions, with expanding geographic distribution and rising reports of atypical and severe manifestations, including neurological involvement. In endemic and resource-limited settings, particularly those affected by conflict, the widespread availability of rapid diagnostic tests and overlapping clinical presentations with other infectious diseases have led to a growing concern: diagnostic anchoring bias toward dengue. This bias...

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Diagnostic Decision Support and Automation in Vestibular Diagnosis

PubMed - neurological misdiagnosis Published 13 Oct 2026 Relevancy: 77%

This article examines the current and future role of decision-support systems and automation in vestibular diagnosis across emergency, primary care, and specialty settings. Vestibular disorders are common but often misdiagnosed because of overlapping symptoms, challenging bedside examinations, and limitations of neuroimaging. Structured diagnostic approaches improve accuracy when correctly applied. Emerging technologies offer objective assessment of eye movements and may enhance diagnostic...

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Homozygous PRRT2 mutation causing a spectrum of paroxysmal neurological symptoms responsive to sodium channel blockers

Practical Neurology - Online First Published 12 Oct 2026 Relevancy: 88%

Case presentation A 17-year-old woman attended the adult outpatient clinic with recent focal seizures, lasting approximately 30s, occurring several times a week. She experienced an odd sensation that she recognised but could not describe, followed by loss of consciousness. Her mother reported she would become blank and stare with swallowing movements. Occasionally, she would turn her head to the left, pluck at her clothes and make a low-pitched groan. These seizures occurred after carbamazepine (taken since early childhood) was weaned. She also reported intermittent tingling sensations, poor memory and hemiplegic migraine (HM). A clinical diagnosis of focal epilepsy, likely temporal, was made. A sleep electroencephalogram (EEG) showed several runs of bitemporal or independent epileptiform discharges, mainly right frontotemporal. Medical history Aged 2 months, she had her first generalised tonic-clonic seizure (GTCS) and was admitted with recurrent seizures, treated with phenobarbital, followed by carbamazepine and became seizure-free. At nearly 4 years of age,...

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