Prediagnostic plasma branched-chain amino acids and the risk of amyotrophic lateral sclerosis

被引:9
作者
Bjornevik, Kjetil [1 ]
O'Reilly, Eilis J. [1 ,3 ]
Berry, James D. [4 ]
Clish, Clary B. [6 ]
Jeanfavre, Sarah [6 ]
Kato, Ikuko [7 ]
Kolonel, Laurence N. [8 ]
Le Marchand, Loic [8 ]
McCullough, Marjorie L. [9 ]
Paganoni, Sabrina [5 ,10 ,11 ]
Schwarzschild, Michael A. [4 ,11 ]
Talbott, Evelyn O. [12 ]
Wallace, Robert B. [13 ]
Zhang, Zhongli [1 ]
Manson, JoAnn E. [2 ,14 ]
Ascherio, Alberto [1 ,2 ,15 ]
机构
[1] Harvard TH Chan Sch Publ Hlth, Dept Nutr, Boston, MA 02115 USA
[2] Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
[3] Univ Coll Cork, Coll Med, Sch Publ Hlth, Cork, Ireland
[4] Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA
[5] Massachusetts Gen Hosp, Boston, MA 02114 USA
[6] Broad Inst Massachusetts Inst Technol & Harvard, Metabol Platform, Cambridge, MA USA
[7] Wayne State Univ, Sch Med, Dept Oncol, Karmanos Canc Inst, Detroit, MI USA
[8] Univ Hawaii, Ctr Canc, Program Epidemiol, Honolulu, HI 96822 USA
[9] Amer Canc Soc, Epidemiol Res Program, Atlanta, GA 30329 USA
[10] Spaulding Rehabil Hosp, Dept Phys Med & Rehabil, Charlestown, MA USA
[11] Harvard Med Sch, Boston, MA 02115 USA
[12] Univ Pittsburgh, Dept Epidemiol, Grad Sch Publ Hlth, Pittsburgh, PA 15260 USA
[13] Univ Iowa, Coll Publ Hlth, Dept Epidemiol, Iowa City, IA USA
[14] Harvard Med Sch, Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[15] Harvard Med Sch, Brigham & Womens Hosp, Channing Div Network Med, Boston, MA 02115 USA
关键词
DISEASE; METABOLOMICS; COHORT; TRIAL; ALS;
D O I
10.1212/WNL.0000000000006669
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective To assess whether prediagnostic levels of plasma branched-chain amino acids (BCAAs) are associated with amyotrophic lateral sclerosis (ALS) risk. Methods We included participants from 5 large cohort studies-The Nurses' Health Study, the Health Professionals Follow-up Study, the Cancer Prevention Study II Nutrition, the Multiethnic Cohort Study, and the Women's Health Initiative-and identified 275 individuals who developed ALS during follow-up. Two controls were randomly selected for each case, matched on cohort, age, sex, fasting status, and time of blood draw. We measured metabolites using liquid chromatography-mass spectrometry and used conditional logistic regression to estimate rate ratios (RRs) and 95% confidence intervals (CIs) for the association of individual BCAAs with ALS risk. Results None of the 3 BCAAs was associated with a higher ALS risk. The risk estimates were similar for leucine (RR top vs bottom quartile: 0.87, 95% CI 0.57-1.33), isoleucine (RR top vs bottom quartile: 0.81, 95% CI 0.52-1.24), and valine (RR top vs bottom quartile: 0.80, 95% CI 0.52-1.23) in a multivariable analysis adjusted for body mass index, smoking, level of education, and physical activity. The estimates did not vary significantly by sex, fasting status, or time interval between blood draw and disease onset. Conclusion The results from this study do not support the hypothesis that BCAAs are risk factors for ALS.
引用
收藏
页码:E2081 / E2088
页数:8
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