Literature DB >> 24522445

Estimating daily energy expenditure in individuals with amyotrophic lateral sclerosis.

Edward J Kasarskis1, Marta S Mendiondo, Dwight E Matthews, Hiroshi Mitsumoto, Rup Tandan, Zachary Simmons, Mark B Bromberg, Richard J Kryscio.   

Abstract

BACKGROUND: Patients with amyotrophic lateral sclerosis (ALS) experience progressive limb weakness, muscle atrophy, and dysphagia, making them vulnerable to insufficient energy intake. Methods to estimate energy requirements have not been devised for this patient group.
OBJECTIVE: The goal was to develop equations to estimate energy requirements of ALS patients.
DESIGN: We enrolled 80 ALS participants at varying stages of their illness and studied them every 16 wk over 48 wk. At each time, we determined total daily energy expenditure (TDEE) in the home setting over a 10-d period by using the doubly labeled water method. We then developed statistical models to estimate TDEE by using factors easily obtained during a routine clinical visit.
RESULTS: The most practical TDEE models used the Harris-Benedict, Mifflin-St Jeor, or Owen equations to estimate resting metabolic rate (RMR) and 6 questions from the revised ALS Functional Rating Scale (ALSFRS-R) that relate to physical activity. We developed a Web-based calculator to facilitate its use. In the research setting, measuring body composition with bioelectrical impedance spectroscopy enabled the estimation of RMR with the Rosenbaum equation and the same 6 questions from the ALSFRS-R to estimate TDEE. By using these models, the estimate of TDEE for nutritional maintenance was ±500 kcal/d across the spectrum of ALS progression.
CONCLUSIONS: Our results emphasize the importance of physical function and body composition in estimating TDEE. Our predictive equations can serve as a basis for recommending placement of a feeding gastrostomy in ALS patients who fail to meet their energy requirements by oral intake.

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Year:  2014        PMID: 24522445      PMCID: PMC3953880          DOI: 10.3945/ajcn.113.069997

Source DB:  PubMed          Journal:  Am J Clin Nutr        ISSN: 0002-9165            Impact factor:   7.045


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  14 in total

Review 1.  Complementary and Alternative Therapies in Amyotrophic Lateral Sclerosis.

Authors:  Richard S Bedlack; Nanette Joyce; Gregory T Carter; Sabrina Paganoni; Chafic Karam
Journal:  Neurol Clin       Date:  2015-09-08       Impact factor: 3.806

2.  Maximum Tongue Pressure is Associated with Swallowing Dysfunction in ALS Patients.

Authors:  Aya Hiraoka; Mineka Yoshikawa; Masahiro Nakamori; Naohisa Hosomi; Toshikazu Nagasaki; Takahiro Mori; Masaya Oda; Hirofumi Maruyama; Mitsuyoshi Yoshida; Yuishin Izumi; Masayasu Matsumoto; Kazuhiro Tsuga
Journal:  Dysphagia       Date:  2017-04-19       Impact factor: 3.438

Review 3.  Symptom Management and End-of-Life Care in Amyotrophic Lateral Sclerosis.

Authors:  Carlayne E Jackson; April L McVey; Stacy Rudnicki; Mazen M Dimachkie; Richard J Barohn
Journal:  Neurol Clin       Date:  2015-11       Impact factor: 3.806

4.  Skeletal-Muscle Metabolic Reprogramming in ALS-SOD1G93A Mice Predates Disease Onset and Is A Promising Therapeutic Target.

Authors:  Silvia Scaricamazza; Illari Salvatori; Giacomo Giacovazzo; Jean Philippe Loeffler; Frederique Renè; Marco Rosina; Cyril Quessada; Daisy Proietti; Constantin Heil; Simona Rossi; Stefania Battistini; Fabio Giannini; Nila Volpi; Frederik J Steyn; Shyuan T Ngo; Elisabetta Ferraro; Luca Madaro; Roberto Coccurello; Cristiana Valle; Alberto Ferri
Journal:  iScience       Date:  2020-04-21

5.  Patient-reported problematic symptoms in an ALS treatment trial.

Authors:  Divisha Raheja; Helen E Stephens; Erik Lehman; Susan Walsh; Chengwu Yang; Zachary Simmons
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2016-01-29       Impact factor: 4.092

6.  Prognostic significance of body weight variation after diagnosis in ALS: a single-centre prospective cohort study.

Authors:  Toshio Shimizu; Yuki Nakayama; Chiharu Matsuda; Michiko Haraguchi; Kota Bokuda; Kazuko Ishikawa-Takata; Akihiro Kawata; Eiji Isozaki
Journal:  J Neurol       Date:  2019-03-13       Impact factor: 4.849

7.  Energy expenditure in frontotemporal dementia: a behavioural and imaging study.

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

Authors:  Rup Tandan; Evan A Levy; Diantha B Howard; John Hiser; Nathan Kokinda; Swatee Dey; Edward J Kasarskis
Journal:  Am J Clin Nutr       Date:  2022-05-01       Impact factor: 8.472

9.  Gastrostomy in patients with amyotrophic lateral sclerosis (ProGas): a prospective cohort study.

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Journal:  Lancet Neurol       Date:  2015-05-28       Impact factor: 44.182

Review 10.  Exploring targets and therapies for amyotrophic lateral sclerosis: current insights into dietary interventions.

Authors:  Shyuan T Ngo; Jia D Mi; Robert D Henderson; Pamela A McCombe; Frederik J Steyn
Journal:  Degener Neurol Neuromuscul Dis       Date:  2017-07-25
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