Changes in the ascertainment of multiple sclerosis
Abstract
Objective With diagnostic criteria alterations, increased MRI availability, and awareness of therapies, temporal changes in incidence and prevalence rates may occur, with an increase in the proportion of mildly affected persons diagnosed with multiple sclerosis (MS). The authors assessed temporal trends in the delay from symptom onset to diagnosis (DONDX), and determined whether the degree of disability at diagnosis differs by year of symptom onset (YONSET), using the NARCOMS Registry. Methods The authors selected US participants with an age at symptom onset of 10 to 60 years, and YONSET > or = 1980 (n = 16,581). The authors divided YONSET into 5-year groups and compared DONDX between groups using multivariate Cox regression. The authors classified participants enrolled within 2 years of diagnosis (n = 5,548) as having mild, moderate, or severe disability using Patient Determined Disease Steps, and assessed the association of disability with YONSET using polytomous logistic regression. Results DONDX decreased with later YONSET (r = -0.43, p Conclusion The delay from symptom onset to diagnosis is steadily decreasing in MS. An increasing proportion of patients with MS have mild disability at diagnosis after accounting for confounders. As the effectiveness of therapies is influenced by disease duration, this has implications for comparison of treatment effects in modern clinical trials to earlier study results.
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Patients with MS often experience a period of diagnostic delay prior to receiving a diagnosis of MS.
“Patients with MS often experience a period of diagnostic delay prior to receiving a diagnosis of MS [8].”
From Functional neurological disorder and multiple sclerosis: a systematic review of misdiagnosis and clinical overlap (2022) · cites this paper as [8]
The reasons for diagnostic delay in MS are multifactorial and often involve systemic barriers to healthcare access.
“The reasons for this are multifactorial, and often involve systemic barriers to healthcare access. Although many studies have reported such diagnostic delay in MS care [8–12], only a few have documented specific misdiagnoses that were responsible for such delays (Table 1).”
From Functional neurological disorder and multiple sclerosis: a systematic review of misdiagnosis and clinical overlap (2022) · cites this paper as [8]
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Walzl, D., Solomon, A. J., & Stone, J. (2022) · Journal of Neurology · doi:10.1007/s00415-021-10436-6 · Cited by 62 · see citing works
Riemann-Lorenz, K., Motl, R. W., Casey, B., Coote, S., Daubmann, A., & Heesen, C. (2021) · Disability and Rehabilitation · doi:10.1080/09638288.2020.1731612 · Cited by 30 · see citing works
- Authors
- Marrie, R. A., Cutter, G., Tyry, T., Hadjimichael, O., Campagnolo, D., & Vollmer, T.
- Affiliations
- Cleveland Clinic (US)
- Venue
- Neurology
- Published
- 2005-10-11
- Volume
- 65
- Issue
- 7
- Pages
- 1066-1070
- ISSN
- 0028-3878 (ISSN-L)
- 1526-632X
- OpenAlex
- W2079691677
- Cited by
- 93
- References
- 0
- Citations by year
- 2025: 3 · 2024: 4 · 2023: 6 · 2022: 3 · 2021: 3 · 2020: 4 · 2019: 2 · 2018: 3 · 2017: 2 · 2016: 7 · 2015: 5 · 2014: 3 · 2013: 8 · 2012: 5
- FWCI
- 3.97
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neurology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
- Health Sciences › Medicine › Family Practice › Clinical Reasoning and Diagnostic Skills
- Health Sciences › Medicine › Oncology › Polyomavirus and related diseases
- Keywords
- multiple sclerosis, delayed diagnosis, mild disabilities, temporal trends in diagnosis, disease duration, NARCOMS registry, Patient-Determined Disease Steps, MRI availability, treatment effect comparison
- MeSH terms
- Adolescent, Adult, Age Factors, Child, Preschool, Disability Evaluation, Female, Humans, Male, Middle Aged, Multiple Sclerosis, Predictive Value of Tests, Prognosis, Registries, Sex Factors, Time Factors, Selection Bias, Incidence, Prevalence, Multivariate Analysis, Age of Onset, Disease Progression, Early Diagnosis, Racial Groups
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