Literature DB >> 35108352

Body composition in amyotrophic lateral sclerosis subjects and its effect on disease progression and survival.

Rup Tandan1,2, Evan A Levy1,2, Diantha B Howard2,3,4, John Hiser2,3,4, Nathan Kokinda2,3,4, Swatee Dey5,6, Edward J Kasarskis5,6.   

Abstract

BACKGROUND: Motor neuron degeneration and malnutrition alter body composition in amyotrophic lateral sclerosis (ALS). Resulting losses of weight, fat mass (FM), and fat-free mass (FFM) shorten survival. Nutritional management relies on body weight or BMI; neither reliably indicates malnutrition nor differentiates body compartments.
OBJECTIVES: We aimed to 1) develop an equation to compute FM and FFM using clinical data, validated against DXA; and 2) examine the effect of computed FM and FFM on disease course and survival.
METHODS: We studied 364 ALS patients from 3 cohorts. In Cohort #1 we used logistic regression on clinical and demographic data to create an equation (test cohort). In Cohort #2 we validated FM and FFM computed using this equation against DXA (validation cohort). In Cohort #3, we examined the effect of computed body composition on disease course and survival.
RESULTS: In Cohort #1 (n = 29) the model incorporated sex, age, BMI, and bulbar-onset to create an equation to estimate body fat: % body fat = 1.73 - [19.80*gender (1 if male or 0 if female)] + [0.25*weight (kg)] + [0.95*BMI (kg/m2)] - (5.20*1 if bulbar-onset or *0 if limb-onset). In Cohort #2 (n = 104), body composition using this equation, compared to other published equations, showed the least variance from DXA values. In Cohort #3 (n = 314), loss of body composition over 6 mo was greater in males. Adjusted survival was predicted by low baseline FM (HR: 1.39; 95% CI: 1.07, 1.80), and loss of FM (HR: 1.87; 95% CI: 1.30, 2.69) and FFM (HR: 1.73; 95% CI: 1.20, 2.49) over 6 mo.
CONCLUSIONS: Our equation broadens the traditional nutritional evaluation in clinics and reliably estimates body composition. Measuring body composition could target FM as a focus for nutritional management to ensure adequate energy intake and complement measures, such as the ALS functional rating scale-revised score and forced vital capacity, currently used.
© The Author(s) 2022. Published by Oxford University Press on behalf of the American Society for Nutrition.

Entities:  

Keywords:  amyotrophic lateral sclerosis; body composition; body mass index; disease progression; dual energy X-ray absorptiometry; fat mass; fat-free mass; nutrition; survival

Mesh:

Year:  2022        PMID: 35108352      PMCID: PMC9071423          DOI: 10.1093/ajcn/nqac016

Source DB:  PubMed          Journal:  Am J Clin Nutr        ISSN: 0002-9165            Impact factor:   8.472


  47 in total

1.  Association between nutritional status and disease severity using the amyotrophic lateral sclerosis (ALS) functional rating scale in ALS patients.

Authors:  Yongsoon Park; Jinhee Park; Yeonsun Kim; Heejoon Baek; Seung Hyun Kim
Journal:  Nutrition       Date:  2015-07-06       Impact factor: 4.008

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

Authors:  Johannes Dorst; Joschka Cypionka; Albert C Ludolph
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2013-08-14       Impact factor: 4.092

3.  The ALS Nutrition/NIPPV Study: design, feasibility, and initial results.

Authors:  Edward J Kasarskis; Marta S Mendiondo; Stephen Wells; Maria S Malguizo; Megan Thompson; Margaret Healey; Richard J Kryscio
Journal:  Amyotroph Lateral Scler       Date:  2011-01

Review 4.  The final word on nutritional screening and assessment in older persons.

Authors:  Emanuele Cereda; Nicola Veronese; Riccardo Caccialanza
Journal:  Curr Opin Clin Nutr Metab Care       Date:  2018-01       Impact factor: 4.294

5.  Assessment of body composition with use of dual-energy x-ray absorptiometry: evaluation and comparison with other methods.

Authors:  M D Jensen; J A Kanaley; L R Roust; P C O'Brien; J S Braun; W L Dunn; H W Wahner
Journal:  Mayo Clin Proc       Date:  1993-09       Impact factor: 7.616

6.  The use of upper extremity anthropometrics in the clinical assessment of patients with amyotrophic lateral sclerosis.

Authors:  E J Kasarskis; S Berryman; T English; J Nyland; J G Vanderleest; A Schneider; R Berger; C McClain
Journal:  Muscle Nerve       Date:  1997-03       Impact factor: 3.217

7.  Early weight loss in amyotrophic lateral sclerosis: outcome relevance and clinical correlates in a population-based cohort.

Authors:  Cristina Moglia; Andrea Calvo; Maurizio Grassano; Antonio Canosa; Umberto Manera; Fabrizio D'Ovidio; Alessandro Bombaci; Enrica Bersano; Letizia Mazzini; Gabriele Mora; Adriano Chiò
Journal:  J Neurol Neurosurg Psychiatry       Date:  2019-01-10       Impact factor: 10.154

8.  Nutritional assessment of amyotrophic lateral sclerosis in routine practice: value of weighing and bioelectrical impedance analysis.

Authors:  Vincent Roubeau; Hélène Blasco; François Maillot; Philippe Corcia; Julien Praline
Journal:  Muscle Nerve       Date:  2015-02-24       Impact factor: 3.217

Review 9.  Nutritional state, energy intakes and energy expenditure of amyotrophic lateral sclerosis (ALS) patients.

Authors:  L Genton; V Viatte; J-P Janssens; A-C Héritier; C Pichard
Journal:  Clin Nutr       Date:  2011-07-27       Impact factor: 7.324

10.  Individuals with amyotrophic lateral sclerosis are in caloric balance despite losses in mass.

Authors:  K L Nau; M B Bromberg; D A Forshew; V L Katch
Journal:  J Neurol Sci       Date:  1995-05       Impact factor: 3.181

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