Life course body mass index and risk and prognosis of amyotrophic lateral sclerosis: results from the ALS registry Swabia

被引:83
作者
Peter, Raphael Simon [1 ]
Rosenbohm, Angela [2 ]
Dupuis, Luc [3 ]
Brehme, Torben [1 ]
Kassubek, Jan [2 ]
Rothenbacher, Dietrich [1 ]
Nagel, Gabriele [1 ]
Ludolph, Albert Christian [2 ]
机构
[1] Ulm Univ, Inst Epidemiol & Med Biometry, Helmholtzstr 22, D-89081 Ulm, Germany
[2] Ulm Univ, Dept Neurol, Ulm, Germany
[3] Univ Strasbourg, INSERM, U1118, Strasbourg, France
关键词
Amyotrophic lateral sclerosis; Body mass index; Weight loss; Weight change; Prognostic factor; Risk factor; Hypermetabolism; SURVIVAL; DIAGNOSIS; MULTICENTER; PROGRESSION; JAPAN; MOUSE; DIET;
D O I
10.1007/s10654-017-0318-z
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Weight loss appears as a strong predictor of survival of patients with amyotrophic lateral sclerosis, yet no data are currently available to describe the life course history of pre-diagnostic body mass index (BMI) in these patients. 393 ALS cases (mean age: 65.8 years, 57.3% men) and 791 controls matched by age and sex from a population-based case-control study of the ALS Registry Swabia were analyzed. Differences of BMI change in cases and controls over time were modeled using a multilevel additive model. In addition, survival in ALS cases by BMI change was modeled using an accelerated failure time model adjusted for prognostic factors. In ALS cases, BMI was consistently higher than in controls in the 20-70 years before the interview. Conditional logistic regression revealed an odds ratio of 1.05 (95% confidence interval (CI) 1.00-1.11, p = 0.041) per 1 kg/m(2) higher BMI 35-45 years before interview. However, a sharp decrease was evident in the BMI of ALS cases about 10 years before disease onset. Moreover, weight loss was strongly associated with shorter survival in ALS patients. Illustrating this, patients with stable weight showed a median survival time of 22.1 (95%-CI 19.2-25.0) months, as compared to 13.4 (95%-CI 10.5-16.3) months for patients with weight loss of 2.5 kg/m(2) over the last 3 months before the interview. Thus, alterations in body weight are present in ALS patients already decades before clinical manifestation of ALS, while weight loss precedes motor symptoms of several years and is associated with poor prognosis.
引用
收藏
页码:901 / 908
页数:8
相关论文
共 31 条
  • [1] Hypermetabolism in ALS patients: an early and persistent phenomenon
    Bouteloup, C.
    Desport, J. -C.
    Clavelou, P.
    Guy, N.
    Derumeaux-Burel, H.
    Ferrier, A.
    Couratier, P.
    [J]. JOURNAL OF NEUROLOGY, 2009, 256 (08) : 1236 - 1242
  • [2] Brooks BR, 2000, AMYOTROPH LATERAL SC, V1, pS79
  • [3] Factors predicting survival in ALS: a multicenter Italian study
    Calvo, Andrea
    Moglia, Cristina
    Lunetta, Christian
    Marinou, Kalliopi
    Ticozzi, Nicola
    Ferrante, Gianluca Drago
    Scialo, Carlo
    Soraru, Gianni
    Trojsi, Francesca
    Conte, Amelia
    Falzone, Yuri M.
    Tortelli, Rosanna
    Russo, Massimo
    Chio, Adriano
    Sansone, Valeria Ada
    Mora, Gabriele
    Silani, Vincenzo
    Volanti, Paolo
    Caponnetto, Claudia
    Querin, Giorgia
    Monsurro, Maria Rosaria
    Sabatelli, Mario
    Riva, Nilo
    Logroscino, Giancarlo
    Messina, Sonia
    Fini, Nicola
    Mandrioli, Jessica
    [J]. JOURNAL OF NEUROLOGY, 2017, 264 (01) : 54 - 63
  • [4] The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function
    Cedarbaum, JM
    Stambler, N
    Malta, E
    Fuller, C
    Hilt, D
    Thurmond, B
    Nakanishi, A
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1999, 169 (1-2) : 13 - 21
  • [5] Desport JC, 2001, AM J CLIN NUTR, V74, P328
  • [6] Patients with elevated triglyceride and cholesterol serum levels have a prolonged survival in amyotrophic lateral sclerosis
    Dorst, J.
    Kuehnlein, P.
    Hendrich, C.
    Kassubek, J.
    Sperfeld, A. D.
    Ludolph, A. C.
    [J]. JOURNAL OF NEUROLOGY, 2011, 258 (04) : 613 - 617
  • [7] High-caloric food supplements in the treatment of amyotrophic lateral sclerosis: A prospective interventional study
    Dorst, Johannes
    Cypionka, Joschka
    Ludolph, Albert C.
    [J]. AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, 2013, 14 (7-8) : 533 - 536
  • [8] Incidence of and risk factors for Motor Neurone Disease in UK women: a prospective study
    Doyle, Pat
    Brown, Anna
    Beral, Valerie
    Reeves, Gillian
    Green, Jane
    [J]. BMC NEUROLOGY, 2012, 12
  • [9] Dyslipidemia is a protective factor in amyotrophic lateral sclerosis
    Dupuis, L.
    Corcia, P.
    Fergani, A.
    De Aguilar, J. -L. Gonzalez
    Bonnefont-Rousselot, D.
    Bittar, R.
    Seilhean, D.
    Hauw, J. -J.
    Lacomblez, L.
    Loeffler, J. -P.
    Meininger, V.
    [J]. NEUROLOGY, 2008, 70 (13) : 1004 - 1009
  • [10] Evidence for defective energy homeostasis in amyotrophic lateral sclerosis:: benefit of a high-energy diet in a transgenic mouse
    Dupuis, L
    Oudart, H
    René, F
    de Aguilar, JLG
    Loeffler, JP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (30) : 11159 - 11164