Hypermetabolism is a deleterious prognostic factor in patients with amyotrophic lateral sclerosis. (22nd November 2017)
- Record Type:
- Journal Article
- Title:
- Hypermetabolism is a deleterious prognostic factor in patients with amyotrophic lateral sclerosis. (22nd November 2017)
- Main Title:
- Hypermetabolism is a deleterious prognostic factor in patients with amyotrophic lateral sclerosis
- Authors:
- Jésus, P.
Fayemendy, P.
Nicol, M.
Lautrette, G.
Sourisseau, H.
Preux, P.‐M.
Desport, J.‐C.
Marin, B.
Couratier, P. - Abstract:
- Abstract : Background and purpose: The aim of this study was to investigate patients with amyotrophic lateral sclerosis in order to determine their nutritional, neurological and respiratory parameters, and survival according to metabolic level. Methods: Nutritional assessment included resting energy expenditure (REE) measured by indirect calorimetry [hypermetabolism if REE variation (ΔREE) > 10%] and fat mass (FM) using impedancemetry. Neurological assessment included the Amyotrophic Lateral Sclerosis Functional Rating Scale‐Revised score. Survival analysis used the Kaplan–Meier method and multivariate Cox model. Results: A total of 315 patients were analysed. Median age at diagnosis was 65.9 years and 55.2% of patients were hypermetabolic. With regard to the metabolic level (ΔREE: < 10%, 10–20% and >20%), patients with ΔREE > 20% initially had a lower FM(29.7% vs. 32.1% in those with ΔREE ≤10%; P = 0.0054). During follow‐up, the median slope of Amyotrophic Lateral Sclerosis Functional Rating Scale‐Revised tended to worsen more in patients with ΔREE > 20% (−1.4 vs. −1.0 points/month in those with ΔREE ≤10%; P = 0.07). Overall median survival since diagnosis was 18.4 months. ΔREE > 20% tended to increase the risk of dying compared with ΔREE ≤10% (hazard ratio, 1.33; P = 0.055). In multivariate analysis, an increased REE:FM ratio was independently associated with death (hazard ratio, 1.005; P = 0.001). Conclusions: Hypermetabolism is present in more than half of patients withAbstract : Background and purpose: The aim of this study was to investigate patients with amyotrophic lateral sclerosis in order to determine their nutritional, neurological and respiratory parameters, and survival according to metabolic level. Methods: Nutritional assessment included resting energy expenditure (REE) measured by indirect calorimetry [hypermetabolism if REE variation (ΔREE) > 10%] and fat mass (FM) using impedancemetry. Neurological assessment included the Amyotrophic Lateral Sclerosis Functional Rating Scale‐Revised score. Survival analysis used the Kaplan–Meier method and multivariate Cox model. Results: A total of 315 patients were analysed. Median age at diagnosis was 65.9 years and 55.2% of patients were hypermetabolic. With regard to the metabolic level (ΔREE: < 10%, 10–20% and >20%), patients with ΔREE > 20% initially had a lower FM(29.7% vs. 32.1% in those with ΔREE ≤10%; P = 0.0054). During follow‐up, the median slope of Amyotrophic Lateral Sclerosis Functional Rating Scale‐Revised tended to worsen more in patients with ΔREE > 20% (−1.4 vs. −1.0 points/month in those with ΔREE ≤10%; P = 0.07). Overall median survival since diagnosis was 18.4 months. ΔREE > 20% tended to increase the risk of dying compared with ΔREE ≤10% (hazard ratio, 1.33; P = 0.055). In multivariate analysis, an increased REE:FM ratio was independently associated with death (hazard ratio, 1.005; P = 0.001). Conclusions: Hypermetabolism is present in more than half of patients with amyotrophic lateral sclerosis. It modifies the body composition at diagnosis, and patients with hypermetabolism >20% have a worse prognosis than those without hypermetabolism. Abstract : Clickhere to view the accompanying paper in this volume. … (more)
- Is Part Of:
- European journal of neurology. Volume 25:Number 1(2018)
- Journal:
- European journal of neurology
- Issue:
- Volume 25:Number 1(2018)
- Issue Display:
- Volume 25, Issue 1 (2018)
- Year:
- 2018
- Volume:
- 25
- Issue:
- 1
- Issue Sort Value:
- 2018-0025-0001-0000
- Page Start:
- 97
- Page End:
- 104
- Publication Date:
- 2017-11-22
- Subjects:
- amyotrophic lateral sclerosis -- hypermetabolism -- nutritional status -- prognosis -- survival
Neurology -- Periodicals
Nervous system -- Diseases -- Periodicals
616.8 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1468-1331 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/ene.13468 ↗
- Languages:
- English
- ISSNs:
- 1351-5101
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3829.731680
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 5607.xml