☆ 4.7 Review

The safety and effectiveness of high-calorie therapy for treating amyotrophic lateral sclerosis: a systematic review and meta-analysis

JOURNAL OF NEUROLOGY (2023)

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Review Pharmacology & Pharmacy

Emerging clinical investigational drugs for the treatment of amyotrophic lateral sclerosis

Loreto Martinez-Gonzalez et al.

Summary: This review provides an overview of the clinical investigational small molecules and biological-based therapies that are currently undergoing clinical trials for the treatment of ALS. Despite the lack of effective treatments, there are many innovative drugs and therapies being developed. Proteostasis, particularly the recovery of functional TDP-43 homeostasis, may be a promising mechanism for modifying ALS progression.

EXPERT OPINION ON INVESTIGATIONAL DRUGS (2023)

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Article Clinical Neurology

Fat-rich versus carbohydrate-rich nutrition in ALS: a randomised controlled study

Johannes Dorst et al.

Summary: This study found that high-caloric food supplements often cause mild to moderate tolerability issues in ALS patients, with gastrointestinal symptoms being most common in high-fat supplements and loss of appetite being most common in high-carbohydrate supplements. All three supplements tested were effective in increasing body weight.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2022)

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Article Nutrition & Dietetics

Dietary-Derived Essential Nutrients and Amyotrophic Lateral Sclerosis: A Two-Sample Mendelian Randomization Study

Kailin Xia et al.

Summary: This study used Mendelian randomization analysis to investigate the potential causal relationship between essential nutrients and the risk of amyotrophic lateral sclerosis (ALS). The study found a causal association between genetically predicted linoleic acid (LA) and ALS risk, and a negative association between vitamin D/vitamin E and ALS risk. No causal effect was observed for essential amino acids and minerals on ALS risk.

NUTRIENTS (2022)

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Review Economics

The economic burden of amyotrophic lateral sclerosis: a systematic review

K. Achtert et al.

Summary: This systematic review collected and summarized 20 studies on the economic burden of amyotrophic lateral sclerosis. Most studies focused on costs per patient, ranging from euro9741 to euro114,605. Six studies demonstrated an increase in costs as the disease progressed, peaking near the patient's death. National costs for amyotrophic lateral sclerosis ranged between euro149 million and euro1329 million.

EUROPEAN JOURNAL OF HEALTH ECONOMICS (2021)

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Article Clinical Neurology

Hypermetabolism is a reality in amyotrophic lateral sclerosis compared to healthy subjects

Philippe Fayemendy et al.

Summary: The study confirmed the presence of hypermetabolism (HM) in ALS patients, with more than half of the patients affected by HM. HM was strongly and positively associated with ALS, indicating a frequent metabolic deterioration during the disease. Identifying HM can facilitate better adaptation of patients' nutritional intake.

JOURNAL OF THE NEUROLOGICAL SCIENCES (2021)

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Review Medicine, General & Internal

PRISMA 2020 explanation and elaboration: updated guidance and exemplars for reporting systematic reviews

Matthew J. Page et al.

Summary: The methods and results of systematic reviews should be reported in sufficient detail to allow users to assess trustworthiness. PRISMA 2020 aims to improve the transparency and completeness of systematic review reporting, in hopes of guiding more accurate and transparent reporting.

BMJ-BRITISH MEDICAL JOURNAL (2021)

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Review Nutrition & Dietetics

Metabolic Abnormalities, Dietary Risk Factors and Nutritional Management in Amyotrophic Lateral Sclerosis

Emanuele D'Amico et al.

Summary: ALS is a devastating neurodegenerative disease that affects motor neurons and leads to muscle paralysis and respiratory failure. Metabolic abnormalities and nutritional factors may play a role in disease progression. Nutritional assessment and maintenance of weight are important for ALS patients, potentially influencing disease progression.

NUTRIENTS (2021)

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Article Neurosciences

Association between macronutrient intake and amyotrophic lateral sclerosis prognosis

Boeun Kim et al.

NUTRITIONAL NEUROSCIENCE (2020)

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Article Clinical Neurology

Effect of High-Caloric Nutrition on Survival in Amyotrophic Lateral Sclerosis

Albert C. Ludolph et al.

ANNALS OF NEUROLOGY (2020)

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Review Biochemistry & Molecular Biology

The potential interplay between energy metabolism and innate complement activation in amyotrophic lateral sclerosis

Tanya S. McDonald et al.

FASEB JOURNAL (2020)

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Article Clinical Neurology

Prognostic value of weight loss in patients with amyotrophic lateral sclerosis: a population-based study

Mark R. Janse van Mantgem et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2020)

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Article Economics

A Cost-Effectiveness Framework for Amyotrophic Lateral Sclerosis, Applied to Riluzole

Nimish J. Thakore et al.

VALUE IN HEALTH (2020)

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Review Health Care Sciences & Services

Lack of transparency in reporting narrative synthesis of quantitative data: a methodological assessment of systematic reviews

Mhairi Campbell et al.

JOURNAL OF CLINICAL EPIDEMIOLOGY (2019)

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Review Chemistry, Medicinal

Riluzole and edaravone: A tale of two amyotrophic lateral sclerosis drugs

Manoj Kumar Jaiswal

MEDICINAL RESEARCH REVIEWS (2019)

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Review Clinical Neurology

Epidemiology of amyotrophic lateral sclerosis: an update of recent literature

Elisa Longinetti et al.

CURRENT OPINION IN NEUROLOGY (2019)

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Review Clinical Neurology

Nutrition management methods effective in increasing weight, survival time and functional status in ALS patients: a systematic review

Jaylin Kellogg et al.

AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION (2018)

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Review Clinical Neurology

Energy metabolism in ALS: an underappreciated opportunity?

Tijs Vandoorne et al.

ACTA NEUROPATHOLOGICA (2018)

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Review Medicine, General & Internal

Amyotrophic lateral sclerosis

Michael A. van Es et al.

LANCET (2017)

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Article Medicine, General & Internal

Amyotrophic lateral sclerosis

Orla Hardiman et al.

NATURE REVIEWS DISEASE PRIMERS (2017)

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Review Clinical Neurology

Pathophysiological and diagnostic implications of cortical dysfunction in ALS

Nimeshan Geevasinga et al.

NATURE REVIEWS NEUROLOGY (2016)

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Review Medicine, General & Internal

Preferred Reporting Items for a Systematic Review and Meta-analysis of Individual Participant Data The PRISMA-IPD Statement

Lesley A. Stewart et al.

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2015)

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Review Clinical Neurology

Natural history and clinical features of sporadic amyotrophic lateral sclerosis in China

Lu Chen et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2015)

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Article Medicine, Research & Experimental

Effects of diet on adenosine monophosphate-activated protein kinase activity and disease progression in an amyotrophic lateral sclerosis model

Zichun Zhao et al.

JOURNAL OF INTERNATIONAL MEDICAL RESEARCH (2015)

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Article Health Care Sciences & Services

Estimating the sample mean and standard deviation from the sample size, median, range and/or interquartile range

Xiang Wan et al.

BMC MEDICAL RESEARCH METHODOLOGY (2014)

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Article Medicine, General & Internal

Hypercaloric enteral nutrition in patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled phase 2 trial

Anne-Marie Wills et al.

LANCET (2014)

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Article Clinical Neurology

High-calorie diet might delay amyotrophic lateral sclerosis

Hemi Malkki

Nature Reviews Neurology (2014)

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Article Clinical Neurology

High-caloric food supplements in the treatment of amyotrophic lateral sclerosis: A prospective interventional study

Johannes Dorst et al.

AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION (2013)

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Article Clinical Neurology

Patients with elevated triglyceride and cholesterol serum levels have a prolonged survival in amyotrophic lateral sclerosis

J. Dorst et al.

JOURNAL OF NEUROLOGY (2011)

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Article Clinical Neurology

Alteration of nutritional status at diagnosis is a prognostic factor for survival of amyotrophic lateral sclerosis patients

B. Marin et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2011)

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Review Clinical Neurology

Energy metabolism in amyotrophic lateral sclerosis

Luc Dupuis et al.

LANCET NEUROLOGY (2011)

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Article Neurosciences

Effect of nutritional supplementation with milk whey proteins in amyotrophic lateral sclerosis patients

Luciano Bruno de Carvalho Silva et al.

ARQUIVOS DE NEURO-PSIQUIATRIA (2010)

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Article Endocrinology & Metabolism

The regulation of AMP-activated protein kinase by upstream kinases

D. Carling et al.

INTERNATIONAL JOURNAL OF OBESITY (2008)

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Review Cell Biology

AMP-activated/SNF1 protein kinases: conserved guardians of cellular energy

D. Grahame Hardie

NATURE REVIEWS MOLECULAR CELL BIOLOGY (2007)

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Article Multidisciplinary Sciences

Evidence for defective energy homeostasis in amyotrophic lateral sclerosis:: benefit of a high-energy diet in a transgenic mouse

L Dupuis et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)

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Article Medicine, General & Internal

Measuring inconsistency in meta-analyses

JPT Higgins et al.

BMJ-BRITISH MEDICAL JOURNAL (2003)

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