Citations 437

Incidence and prevalence of multiple sclerosis in Olmsted County, Minnesota, 1985–2000

Neurology | May 13, 2012 | Volume: 61 | Issue: 10 | Pages: 1373-1377

10.1212/01.wnl.0000094316.90240.eb | PMID 14638958

Emerging synaptic biomarkers in autoimmune dementia

Neurology | April 27, 2012 | Volume: 78 | Issue: 22 | Pages: 1710-1711

10.1212/wnl.0b013e31825830f3 | PMID 22539567

Do not treat from CIS onset: evaluate disease course and prognosis first – Yes

Multiple Sclerosis Journal | April 3, 2012 | Volume: 18 | Issue: 4 | Pages: 391-393

10.1177/1352458512440604 | PMID 22473500

As physicians how do we counsel our patients with clinically isolated syndrome (CIS) when they ask, ‘what is the benefit of injecting disease-modifying agents (DMAs) over many years? What disability will they prevent in my future?’ In this debate, we will provide three core points supporting the concept that a watchful waiting approach (annual neurological evaluation and magnetic resonance imaging of the head (with gadolinium) at least for the first few years after diagnosis) for most patients with CIS represents appropriate medical care.
Serologic diagnosis of NMO

Neurology | February 2, 2012 | Volume: 78 | Issue: 9 | Pages: 665-671

10.1212/wnl.0b013e318248dec1 | PMID 22302543

Syndrome of inappropriate antidiuresis may herald or accompany neuromyelitis optica

Neurology | October 14, 2011 | Volume: 77 | Issue: 17 | Pages: 1644-1646

10.1212/wnl.0b013e3182343377 | PMID 21998320

Statin therapy and multiple sclerosis disability in a population-based cohort

Multiple Sclerosis Journal | September 9, 2011 | Volume: 18 | Issue: 3 | Pages: 358-363

10.1177/1352458511421920 | PMID 21908483

Background: Axonal damage and inflammatory demyelination both occur in multiple sclerosis (MS). Some studies suggest that statins, through pleiotropic effects, reduce inflammatory episodes and protect neurons. However, other studies suggest statins have disparate impacts on these pathologic processes. Objective: The objective of this study was to assess disability progression in MS patients receiving statin therapy. Methods: We performed a retrospective medical record review of an established population-based MS prevalence cohort in Olmsted County, Minnesota, comparing disability progression between patients receiving statins and controls. Results: Duration of statin use ranged from 1.9 to 20.3 years with a mean and standard deviation of 6.8 ± 4 years. Years between assessments ranged from 0.6 to 8.2 (75% of patients having intervals >6.4 years). The median (interquartile range) absolute change of disability among the statin group was 0 (0 to +1), compared with +0.5 (0, +1) in the no-statin group. Distributions were not significantly different ( p = 0.39). The mean (standard deviation) absolute change of disability scores among the statin group was +0.69 (+1.49), not significantly different from +0.61 (+1.31) in the no-statin group. Likewise, annualized disability scores did not differ significantly ( p = 0.23). Eighteen (40%) patients worsened by 1.0 or more on Expanded Disability Status Scale (EDSS) in the statin group and 36 (40%) in the no-statin group ( p = 0.85, chi-squared test). Conclusions: In this cohort, disability progression did not differ between those receiving statin therapy and controls. These findings support the hypothesis that statins, in doses currently prescribed for hyperlipidemia, do not affect the long-term course of MS.
Azathioprine

Neurology | August 4, 2011 | Volume: 77 | Issue: 7 | Pages: 659-666

10.1212/wnl.0b013e31822a2780 | PMID 21813788

Paraneoplastic isolated myelopathy

Neurology | June 14, 2011 | Volume: 76 | Issue: 24 | Pages: 2089-2095

10.1212/wnl.0b013e31821f468f | PMID 21670438

CSF complements serum for evaluating paraneoplastic antibodies and NMO-IgG

Neurology | March 21, 2011 | Volume: 76 | Issue: 12 | Pages: 1108-1110

10.1212/wnl.0b013e318211c379 | PMID 21422462

Neuromyelitis optica unique area postrema lesions

Neurology | March 3, 2011 | Volume: 76 | Issue: 14 | Pages: 1229-1237

10.1212/wnl.0b013e318214332c | PMID 21368286