Literature DB >> 30564498

Body mass index and survival from amyotrophic lateral sclerosis: A meta-analysis.

Efthimios Dardiotis1, Vasileios Siokas1, Maria Sokratous1, Zisis Tsouris1, Athina-Maria Aloizou1, Desponia Florou1, Metaxia Dastamani1, Alexios-Fotios A Mentis1, Alexandros G Brotis1.   

Abstract

BACKGROUND: Several studies have examined the relationship between body mass index (BMI) and survival from amyotrophic lateral sclerosis (ALS). Many indicate that low BMI at diagnosis or during follow-up may be associated with accelerated progression and shortened survival. This study systematically evaluated the relationship between BMI and survival in patients with ALS.
METHODS: The PubMed database was searched to identify all available studies reporting time-to-event data. Eight studies with 6,098 patients fulfilled the eligibility criteria. BMI was considered a continuous and ordered variable. Interstudy heterogeneity was assessed by the Cochran Q test and quantified by the I2 metric. Fixed- or random-effects odds ratios summarized pooled effects after taking interstudy variability into account. Significance was set at p < 0.05.
RESULTS: The ALS survival hazard ratio (HR) decreased approximately by 3% (95% confidence interval [CI]: 2%-5%) for each additional BMI unit when BMI was considered a continuous variable. When BMI was considered a categorical variable, the HRs for "normal" BMI vs "overweight" BMI and "obese" BMI were estimated to be as high as 0.91 (95% CI: 0.79-1.04) and 0.78 (95% CI: 0.60-1.01), respectively. The HR for the comparison of the "normal" BMI vs "underweight" BMI was estimated to be as high as 1.94 (95% CI: 1.42-2.65).
CONCLUSIONS: BMI is significantly and inversely associated with ALS survival.

Entities:  

Year:  2018        PMID: 30564498      PMCID: PMC6276330          DOI: 10.1212/CPJ.0000000000000521

Source DB:  PubMed          Journal:  Neurol Clin Pract        ISSN: 2163-0402


  52 in total

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6.  Malnutrition at the time of diagnosis is associated with a shorter disease duration in ALS.

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6.  Peak expiratory flow is a reliably household pulmonary function parameter correlates with disease severity and survival of patients with amyotrophic lateral sclerosis.

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  9 in total

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