Vitamin D status predicts new brain magnetic reso… [Ann Neurol. 2012] – PubMed – NCBI

Ann Neurol. 2012 Aug;72(2):234-40. doi: 10.1002/ana.23591.

Vitamin D status predicts new brain magnetic resonance imaging activity in multiple sclerosis.

Source

Multiple Sclerosis Center, Department of Neurology, University of California at San Francisco, San Francisco, CA, USA. emowry1@jhmi.edu

Abstract

OBJECTIVE:

We sought to determine whether vitamin D status is associated with developing new T2 lesions or contrast-enhancing lesions on brain magnetic resonance imaging (MRI) in relapsing multiple sclerosis (MS).

METHODS:

EPIC is a 5-year longitudinal MS cohort study at the University of California at San Francisco. Participants had clinical evaluations, brain MRI, and blood draws annually. From the overall cohort, we evaluated patients with clinically isolated syndrome or relapsing-remitting MS at baseline. In univariate and multivariate (adjusted for age, sex, ethnicity, smoking, and MS treatments) repeated measures analyses, annual 25-hydroxyvitamin D levels were evaluated for their association with subsequent new T2-weighted and gadolinium-enhancing T1-weighted lesions on brain MRI, clinical relapses, and disability (Expanded Disability Status Scale [EDSS]).

RESULTS:

A total of 2,362 3T brain MRI scans were acquired from 469 subjects. In multivariate analyses, each 10ng/ml higher 25-hydroxyvitamin D level was associated with a 15% lower risk of a new T2 lesion (incidence rate ratio [IRR], 0.85; 95% confidence interval [CI], 0.76-0.95; p = 0.004) and a 32% lower risk of a gadolinium-enhancing lesion (IRR, 0.68; 95% CI, 0.53-0.87; p = 0.002). Each 10ng/ml higher vitamin D level was associated with lower subsequent disability (-0.047; 95% CI, -0.091 to -0.003; p = 0.037). Higher vitamin D levels were associated with lower, but not statistically significant, relapse risk. Except for the EDSS model, all associations were stronger when the within-person change in vitamin D level was the predictor.

INTERPRETATION:

Vitamin D levels are inversely associated with MS activity on brain MRI. These results provide further support for a randomized trial of vitamin D supplementation.

Copyright © 2012 American Neurological Association.

PMID:
22926855
[PubMed – indexed for MEDLINE]
PMCID:
PMC3430977
[Available on 2013/8/1]

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The influence of nutritional factors on the prognosis of multiple sclerosis : Article : Nature Reviews Neurology

 

 

Nature Reviews Neurology 8, 678-689 (December 2012) | doi:10.1038/nrneurol.2012.194

Subject Categories: Neuroimmunology and neuroinflammation | White matter disease

The influence of nutritional factors on the prognosis of multiple sclerosis

Gloria von Geldern & Ellen M. Mowry  About the authors

The effect of nutrition and dietary supplements on the course of multiple sclerosis (MS) is a topic of great interest to both patients and clinicians. In particular, vitamin D status has been shown to influence both the incidence and the course of MS. High vitamin D levels are probably protective against the development of MS, although the efficacy of vitamin D supplementation in slowing progression of MS remains to be established. The influence of polyunsaturated fatty acids (PUFAs) on the development and course of MS has also long been under investigation. Small clinical trials suggest a modest reduction in the severity and duration of relapses in patients with MS receiving PUFA supplements. Other nutritional factors have been evaluated for their effect on MS disease progression, including milk proteins, gluten, probiotics, antioxidants (uric acid, vitamins A, C and E, lipoic acid), polyphenols, Ginkgo biloba extracts and curcumin. However, further studies are needed to evaluate the effects of these dietary components on the relapse rate and progression of MS. This Review gives an overview of the literature on the nutritional factors most commonly implicated as having an effect on MS and discusses the biological rationale that is thought to underlie their influence.

Key points
  • Dietary changes and nutritional supplements are widely used by patients with multiple sclerosis (MS), but reliable evidence of their risks, benefits, and underlying mechanisms is limited
  • In observational studies, low vitamin D levels are associated with a worse course of disease in patients with MS
  • Polyunsaturated fatty acid supplementation and a low-fat diet attenuate MS immune responses in vitro and in animal models, but limited trials have shown no clear benefit in patients with MS
  • Antioxidants, probiotics and vitamin B12 supplementation attenuate MS immune responses in vitro and reduce disease symptoms in animal models, but data from human studies are limited
  • Milk proteins and gluten are thought to worsen the outcomes of patients with MS, but no randomized controlled trials have assessed the effect of dietary restrictions in this setting

 

via The influence of nutritional factors on the prognosis of multiple sclerosis : Article : Nature Reviews Neurology.

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Can MRI screen for CSF biomarkers in neurodegenerative disease?

Imaging advances are always potentially interesting but the immediate risk might be more dementia diagnoses delivered without much regard to functional context, and without proper support and follow-up.

Can MRI screen for CSF biomarkers in neurodegenerative disease?

  1. Corey T. McMillan, PhD,
  2. Brian Avants, PhD,
  3. David J. Irwin, MD,
  4. Jon B. Toledo, MD,
  5. David A. Wolk, MD,
  6. Vivianna M. Van Deerlin, MD, PhD,
  7. Leslie M. Shaw, PhD,
  8. John Q. Trojanoswki, MD, PhD and
  9. Murray Grossman, MD, EdD

+ Author Affiliations


  1. From the Department of Neurology (C.T.M., D.J.I., D.A.W., M.G.), Center for Neurodegenerative Disease Research (D.J.I., J.B.T., V.M.V.D., L.M.S., J.Q.T.), Department of Radiology (B.A.), Penn Memory Center (D.A.W.), and Department of Pathology & Laboratory Medicine (V.M.V.D., L.M.S., J.Q.T.), University of Pennsylvania, Philadelphia.
  1. Correspondence to Dr. McMillan: mcmillac@mail.med.upenn.edu

View Complete Disclosures

Abstract

Objective: Alzheimer disease (AD) and frontotemporal lobar degeneration (FTLD) may have overlapping clinical presentations despite distinct underlying neuropathologies, thus making in vivo diagnosis challenging. In this study, we evaluate the utility of MRI as a noninvasive screening procedure for the differential diagnosis of AD and FTLD.

Methods: We recruited 185 patients with a clinically diagnosed neurodegenerative disease consistent with AD or FTLD who had a lumbar puncture and a volumetric MRI. A subset of 32 patients had genetic or autopsy-confirmed AD or FTLD. We used singular value decomposition to decompose MRI volumes and linear regression and cross-validation to predict CSF total tau (tt) and β-amyloid (Aβ1-42) ratio (tt/Aβ) in patients with AD and patients with FTLD. We then evaluated accuracy of MRI-based predicted tt/Aβ using 4 converging sources including neuroanatomic visualization and categorization of a subset of patients with genetic or autopsy-confirmed AD or FTLD.

Results: Regression analyses showed that MRI-predicted tt/Aβ is highly related to actual CSF tt/Aβ. In each group, both predicted and actual CSF tt/Aβ have extensively overlapping neuroanatomic correlates: low tt/Aβ consistent with FTLD is related to ventromedial prefrontal regions while high tt/Aβ consistent with AD is related to posterior cortical regions. MRI-predicted tt/Aβ is 75% accurate at identifying underlying diagnosis in patients with known pathology and in clinically diagnosed patients with known CSF tt/Aβ levels.

Conclusion: MRI may serve as a noninvasive procedure that can screen for AD and FTLD pathology as a surrogate for CSF biomarkers.

Footnotes

  • Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Editorial, page 126

  • Supplemental data at www.neurology.org

  • Received May 17, 2012.
  • Accepted August 14, 2012.

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Scientists plead for urgent action to tackle the growing dementia crisis | Society | The Observer

Scientists plead for urgent action to tackle the growing dementia crisis

As the number of sufferers from dementia nears a million, and drugs companies fail to find therapies that work, doctors fear services may soon become overwhelmed

via Scientists plead for urgent action to tackle the growing dementia crisis | Society | The Observer.

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Time to confront the global dementia crisis : The Lancet Neurology

Time to confront the global dementia crisis

The Lancet Neurology

High-income countries are not the only ones facing a dementia crisis as their populations age. According to the Alzheimer’s Disease International (ADI) Delphi consensus study, by 2040, 71% of all people with dementia will be living in developing countries. In addition to the personal devastation for these 58 million people and their families, the economic burden is likely to be immense: in this issue of The Lancet Neurology, Kalaria and colleagues estimate that the total costs of ageing-related dementia in developing countries were already more than US$70 billion per year in 2005, when prevalence was only 15 million. Despite the scale of the problem, there is relatively little research into dementia in developing nations—just 10% has focussed on countries where more than 66% of people with these disorders live. The 10/66 Dementia Research Group, which celebrates its tenth anniversary at the end of August, is working with ADI to address this imbalance, but dementia in the developing world remains dangerously neglected within communities, by researchers, and by policy makers.

Greater awareness, policy change, and development of health-care services all stem from good research. Over the past decade, through collaborations between researchers in developed and developing countries, the 10/66 group has begun to quantify the occurrence of dementia in low-income and middle-income countries. This major undertaking has included development of more sensitive methods to diagnose dementia, because previous standard assessments are inappropriate in many settings—no-one will do well on a clock-drawing test if they are not familiar with clocks or drawing. 10/66 has also assessed availability of care, and the effects of care-giving on families. Their research, and the work of ADI and its 77 national member associations, is already starting to increase awareness at the community and primary-care levels. For example, after a successful randomised trial in India, the 10/66 research group’s “helping carers to care” initiative is now being rolled out in other countries.

These achievements should not detract from the challenges that remain. Dementia is under-diagnosed in many societies owing to stigma or misclassification as normal ageing. Reliable prevalence data are available for only two countries in Africa, and even less is known about the prevalence of different dementia types. How prevalence, incidence, and survival are affected by ethnic subgroup or economic status remain largely unknown. Better understanding of dementia in developing countries is likely to provide valuable new information on risk factors, genetics, and potential new treatments. Lower age-adjusted rates of Alzheimer’s disease in Nigeria and India than in high-income countries could reflect differences in lifestyle or genetics—for example, APOE ɛ4 is not a risk factor for Alzheimer’s disease in several sub-Saharan African populations. Traditional medicines such as some Chinese herbs are also a promising source of potential new treatments. Collaborations between researchers in developing and developed countries will benefit all parties.

But research and grass-roots implementation of care strategies can take us only so far. Unfortunately, the problem of dementia in developing countries is still largely neglected by governments and international funding agencies. While high-profile initiatives such as the Global Fund to Fight AIDS, Tuberculosis, and Malaria have increased awareness about infectious diseases, other diseases have been left behind. When non-communicable diseases have made their way on to the global health policy agenda, the focus has been on cardiovascular disease, diabetes, and cancer, with no mention of dementia. Estimates suggest that similar numbers of people had dementia worldwide in 2007 as had HIV/AIDS—about 33 million in each case. The proportions of these people who were living in developing countries were given at about 95% for HIV/AIDS and 60—70% for dementia. Figures for aid awarded to dementia initiatives in developing countries are scarce, but they are likely to be a tiny fraction of the 25% of international health-care aid currently ear-marked for HIV/AIDS. This difference is in large part attributable to advocacy: unfortunately, patients with dementia in developing countries are rarely in a position to campaign about their disorder.

In addition to their ongoing research, over the next 2 years the 10/66 Dementia Research Group aims to increase awareness of dementia in developing countries at the regional, national, and international levels. Their plans include regular policy briefings based on results from their population surveys, and annual forums for policy makers. When these initiatives begin, governments and international funding agencies must listen. Further neglect of this issue is unacceptable in the face of a global dementia epidemic with which even high-income countries are expected to struggle.

via Time to confront the global dementia crisis : The Lancet Neurology.

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