Statin Medications and Amyotrophic Lateral Sclerosis Incidence and Mortality

被引:11
作者
Weisskopf, Marc G. [1 ,2 ]
Levy, Joseph [3 ]
Dickerson, Aisha S. [4 ]
Paganoni, Sabrina [5 ,6 ]
Leventer-Roberts, Maya [3 ,7 ]
机构
[1] Harvard TH Chan Sch Publ Hlth, Dept Environm Hlth, Boston, MA 02115 USA
[2] Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[3] Clalit Res Inst, Tel Aviv, Israel
[4] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA
[5] Massachusetts Gen Hosp, Sean M Healey & AMG Ctr ALS, Boston, MA 02114 USA
[6] Harvard Med Sch Spaulding Rehabil Hosp, Dept PM & R, Boston, MA USA
[7] Icahn Sch Med Mt Sinai New York, Dept Environm Med, Pediat, New York, NY USA
基金
美国国家卫生研究院;
关键词
amyotrophic lateral sclerosis; epidemiology; hydroxymethylglutaryl-CoA reductase inhibitors; incidence; survival; RISK; SMOKING; SAFETY; ATORVASTATIN; SIMVASTATIN; PROGRESSION; SELECTION; SURVIVAL; DISEASE; DEATH;
D O I
10.1093/aje/kwac054
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Studies of statins and amyotrophic lateral sclerosis (ALS) incidence and survival have had conflicting findings possibly related to difficulties with confounding by indication. We considered potency of statins used and duration of use to explore confounding by indication. Within the Clalit Health Services in Israel, we identified 948 ALS case patients from 2004 through 2017 and matched them with 1,000 control subjects each. Any statin use up to 3 years before ALS onset was not associated with ALS incidence but was associated with a reduced hazard ratio (HR) for death. Odds of ALS did not vary by statin potency, but use of only lower-potency statins was associated with longer survival (HR = 0.82, 95% CI: 0.68, 0.98), whereas the association with higher-potency statins was null compared with those case patients who did not use statins. However, duration of statin use appeared to account for these findings. Those who used statins only up to 3 years had longer survival (HR = 0.77, 95% CI: 0.61, 0.96) than did case patients who did not use statins, but those who used statins for >3 years did not. Although other explanations are possible, these findings could suggest a protective effect of statins on ALS survival that is partially masked by a worse prognosis from underlying reasons for taking statins that deserves further exploration.
引用
收藏
页码:1248 / 1257
页数:10
相关论文
共 50 条
  • [41] Incidence and prevalence of amyotrophic lateral sclerosis in an HMO of Buenos Aires, Argentina
    Bettini, Mariela
    Vicens, Jimena
    Hernan Giunta, Diego
    Rugiero, Marcelo
    Cristiano, Edgardo
    AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, 2013, 14 (7-8) : 598 - 603
  • [42] Serum Proteome in a Sporadic Amyotrophic Lateral Sclerosis Geographical Cluster
    De Benedetti, Stefano
    Gianazza, Elisabetta
    Banfi, Cristina
    Marocchi, Alessandro
    Lunetta, Christian
    Penco, Silvana
    Bonomi, Francesco
    Iametti, Stefania
    PROTEOMICS CLINICAL APPLICATIONS, 2017, 11 (11-12)
  • [43] Antecedent Disease and Amyotrophic Lateral Sclerosis: What Is Protecting Whom?
    Hollinger, Sabrina K.
    Okosun, Ike S.
    Mitchell, Cassie S.
    FRONTIERS IN NEUROLOGY, 2016, 7
  • [44] Incidence of amyotrophic lateral sclerosis in the United States, 2014-2016
    Mehta, Paul
    Raymond, Jaime
    Punjani, Reshma
    Larson, Theodore
    Han, Moon
    Bove, Frank
    Horton, D. Kevin
    AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, 2022, 23 (5-6) : 378 - 382
  • [45] Characteristics and Prognosis of Oldest Old Subjects with Amyotrophic Lateral Sclerosis
    Dandaba, Meira
    Couratier, Philippe
    Labrunie, Anais
    Nicol, Marie
    Hamidou, Bello
    Raymondeau, Marie
    Logroscino, Giancarlo
    Preux, Pierre Marie
    Marin, Benoit
    NEUROEPIDEMIOLOGY, 2017, 49 (1-2) : 64 - 73
  • [46] Epidemiological and clinical features of amyotrophic lateral sclerosis in a Tunisian cohort
    Kacem, Imen
    Sghaier, Ikram
    Bougatef, Sabrine
    Nasri, Amina
    Gargouri, Amina
    Ajroud-Driss, Senda
    Gouider, Riadh
    AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, 2020, 21 (1-2) : 131 - 139
  • [47] The cumulative incidence of dysphagia and dysphagia-free survival in persons diagnosed with amyotrophic lateral sclerosis
    Perry, Bridget J.
    Nelson, Jason
    Wong, John B.
    Kent, David M.
    MUSCLE & NERVE, 2021, 64 (01) : 83 - 86
  • [48] Incidence and prevalence of amyotrophic lateral sclerosis in urban China: a national population-based study
    Xu, Lu
    Chen, Lu
    Wang, Shengfeng
    Feng, Jingnan
    Liu, Lili
    Liu, Guozhen
    Wang, Jinxi
    Zhan, Siyan
    Gao, Pei
    Fan, Dongsheng
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2020, 91 (05) : 520 - 525
  • [49] Incidence of and Mortality From Amyotrophic Lateral Sclerosis in National Football League Athletes
    Daneshvar, Daniel H.
    Mez, Jesse
    Alosco, Michael L.
    Baucom, Zachary H.
    Mahar, Ian
    Baugh, Christine M.
    Valle, Jhaqueline P.
    Weuve, Jennifer
    Paganoni, Sabrina
    Cantu, Robert C.
    Zafonte, Ross D.
    Stern, Robert A.
    Stein, Thor D.
    Tripodis, Yorghos
    Nowinski, Christopher J.
    McKee, Ann C.
    JAMA NETWORK OPEN, 2021, 4 (12)
  • [50] Percutaneous endoscopic gastrostomy in patients with amyotrophic lateral sclerosis: mortality and complications
    Carbo Perseguer, J.
    Madejon Seiz, A.
    Romero Portales, M.
    Martinez Hernandez, J.
    Mora Pardina, J. S.
    Garcia-Samaniego, J.
    NEUROLOGIA, 2019, 34 (09): : 582 - 588