Lanzamiento Enero 2027

Ensayo controlado aleatorizado2015

Effect of creatine monohydrate on clinical progression in patients with Parkinson disease: a randomized clinical trial

Writing Group for the NINDS Exploratory Trials in Parkinson Disease (NET-PD) Investigators, Kieburtz K, Tilley BC, Elm JJ, Babcock D, Hauser R, Ross GW, Augustine AH, Augustine EU, Aminoff MJ, Bodis-Wollner IG, Boyd J, Cambi F, Chou K, Christine CW, Cines M, Dahodwala N, Derwent L, Dewey RB, Hawthorne K, Houghton DJ, Kamp C, Leehey M, Lew MF, Liang GS, Luo ST, Mari Z, Morgan JC, Parashos S, Pérez A, Petrovitch H, Rajan S, Reichwein S, Roth JT, Schneider JS, Shannon KM, Simon DK, Simuni T, Singer C, Sudarsky L, Tanner CM, Umeh CC, Williams K, Wills AM

JAMA · 180 citas

Cómo se estudió

Diseño
Ensayo controlado aleatorizado (indexado por PubMed)
Estudiado en
Personas
Resultado principal
Marcadores de salud y funcionamiento

Quién lo pagó

Financiación
Financiación independiente
Gobierno
National Institute on Aging
Gobierno
National Institute of Neurological Disorders and Stroke
Gobierno
National Center for Research Resources
Gobierno
National Center for Advancing Translational Sciences
Gobierno
National Institute on Minority Health and Health Disparities
Gobierno
NINDS NIH HHS
Gobierno
NIMHD NIH HHS
Gobierno
NIA NIH HHS
Gobierno
NCATS NIH HHS
Gobierno
NCRR NIH HHS
Subvenciones
National Institute of Neurological Disorders and Stroke (U10 NS044504); National Institute of Neurological Disorders and Stroke (K-12NS 066098); National Center for Advancing Translational Sciences (UL1 TR000433); National Center for Research Resources (UL1 RR 025758); National Institute on Aging (K23AG034236); National Institute of Neurological Disorders and Stroke (P50NS091856); National Institute of Neurological Disorders and Stroke (K23 NS072283); National Institute of Neurological Disorders and Stroke (U10 NS044545); National Institute of Neurological Disorders and Stroke (U01 NS43128); National Institute of Neurological Disorders and Stroke (U01NS 043128); National Institute on Minority Health and Health Disparities (R24 MD001779); National Institute of Neurological Disorders and Stroke (NS44504-08); National Institute of Neurological Disorders and Stroke (U10 NS044460)

Según 10 financiadores declarados.

Publicación

Publicado
2015-02-10 · JAMA · vol. 313 · número 6 · pág. 584
Editorial
American Medical Association
Citado
242 citas · más que el 100% de estudios similares · 18.9× el promedio de su campo
Impacto
Entre el 10 % más citado de su campo
Referencias
32 trabajos
Acceso
Acceso abierto (copia en repositorio)
Áreas de investigación
Parkinson's Disease Mechanisms and Treatments · Muscle metabolism and nutrition · Nutrition and Health in Aging
Palabras clave
Medicine, Physical therapy, Randomized controlled trial, Clinical trial, Placebo, Ambulatory, Creatine, Internal medicine, Pediatrics, Alternative medicine, Pathology
MeSH
humans, parkinson disease, disease progression, creatine, antiparkinson agents, treatment outcome, drug therapy, combination, follow-up studies, double-blind method, aged, middle aged, female, male, medication adherence

43 autores

  • Karl Kieburtz🇺🇸 · autor de correspondenciaUniversity of Rochester
  • Barbara C. Tilley🇺🇸The University of Texas Health Science Center at Houston
  • Jordan J. Elm🇺🇸Medical University of South Carolina
  • Debra Babcock🇺🇸National Institutes of Health
  • Robert A. Hauser🇺🇸University of South Florida
  • G. Webster Ross🇺🇸Pacific Health Research and Education Institute
  • Alicia H. Augustine🇺🇸University of Rochester
  • Erika Augustine🇺🇸University of Rochester
  • Michael J. Aminoff🇺🇸University of California, San Francisco
  • Ivan G. Bodis-Wollner🇺🇸State University of New York; SUNY Downstate Health Sciences University; University at Albany, State University of New York
  • James T. Boyd🇺🇸University of Vermont
  • Franca Cambi🇺🇸University of Kentucky
  • Kelvin L. Chou🇺🇸University of Michigan
  • Chadwick W. Christine🇺🇸University of California, San Francisco
  • Michelle Cines🇺🇸University of Maryland, Baltimore
  • Nabila A. Dahodwala🇺🇸University of Pennsylvania; Philadelphia University
  • Lorelei Derwent🇨🇦University of Calgary
  • Richard B. Dewey🇺🇸The University of Texas Southwestern Medical Center
  • Katherine Hawthorne🇺🇸University of Southern California
  • David J. Houghton🇺🇸Ochsner Medical Center
  • Cornelia Kamp🇺🇸University of Rochester
  • Maureen A. Leehey🇺🇸University of Colorado Denver
  • Mark Lew🇺🇸University of Southern California
  • Grace S. Lin Liang🇺🇸Parkinson's Institute and Clinical Center
  • Sheng Luo🇺🇸The University of Texas Health Science Center at Houston
  • Zoltan K. Mari🇺🇸Johns Hopkins University
  • John C. Morgan🇺🇸Augusta University; Georgia Regents Medical Center
  • Sotirios Andreas Parashos
  • Adriana Pérez🇺🇸The University of Texas Health Science Center at Houston
  • Helen Petrovitch🇺🇸Pacific Health Research and Education Institute
  • Suja S. Rajan🇺🇸The University of Texas Health Science Center at Houston
  • Sue Reichwein🇺🇸University of Pennsylvania; Philadelphia University
  • Jessie Tatsuno Roth🇺🇸University of California, San Francisco
  • Jay S. Schneider🇺🇸Thomas Jefferson University
  • Kathleen M. Shannon🇺🇸Rush University Medical Center
  • David K. Simon🇺🇸Beth Israel Deaconess Medical Center; Harvard University Press
  • Tanya Simuni🇺🇸Northwestern University
  • Carlos Singer🇺🇸University of Miami
  • Lewis R. Sudarsky🇺🇸Brigham and Women's Hospital; Harvard University Press
  • Caroline M. Tanner🇺🇸Parkinson's Institute and Clinical Center
  • Chizoba C. Umeh🇺🇸Brigham and Women's Hospital; Harvard University Press
  • Karen Williams🇺🇸Northwestern University
  • Anne-Marie A. Wills🇺🇸Brigham and Women's Hospital; Harvard University Press

Resumen

El texto original del estudio, en el idioma en que se publicó.

Importance

There are no treatments available to slow or prevent the progression of Parkinson disease, despite its global prevalence and significant health care burden. The National Institute of Neurological Disorders and Stroke Exploratory Trials in Parkinson Disease program was established to promote discovery of potential therapies.

Objective

To determine whether creatine monohydrate was more effective than placebo in slowing long-term clinical decline in participants with Parkinson disease.

Design, setting, and patients

The Long-term Study 1, a multicenter, double-blind, parallel-group, placebo-controlled, 1:1 randomized efficacy trial. Participants were recruited from 45 investigative sites in the United States and Canada and included 1741 men and women with early (within 5 years of diagnosis) and treated (receiving dopaminergic therapy) Parkinson disease. Participants were enrolled from March 2007 to May 2010 and followed up until September 2013.

Interventions

Participants were randomized to placebo or creatine (10 g/d) monohydrate for a minimum of 5 years (maximum follow-up, 8 years).

Main outcomes and measures

The primary outcome measure was a difference in clinical decline from baseline to 5-year follow-up, compared between the 2 treatment groups using a global statistical test. Clinical status was defined by 5 outcome measures: Modified Rankin Scale, Symbol Digit Modalities Test, PDQ-39 Summary Index, Schwab and England Activities of Daily Living scale, and ambulatory capacity. All outcomes were coded such that higher scores indicated worse outcomes and were analyzed by a global statistical test. Higher summed ranks (range, 5-4775) indicate worse outcomes.

Results

The trial was terminated early for futility based on results of a planned interim analysis of participants enrolled at least 5 years prior to the date of the analysis (n = 955). The median follow-up time was 4 years. Of the 955 participants, the mean of the summed ranks for placebo was 2360 (95% CI, 2249-2470) and for creatine was 2414 (95% CI, 2304-2524). The global statistical test yielded t1865.8 = -0.75 (2-sided P = .45). There were no detectable differences (P < .01 to partially adjust for multiple comparisons) in adverse and serious adverse events by body system.

Conclusions and relevance

Among patients with early and treated Parkinson disease, treatment with creatine monohydrate for at least 5 years, compared with placebo did not improve clinical outcomes. These findings do not support the use of creatine monohydrate in patients with Parkinson disease.

Trial registration

clinicaltrials.gov Identifier: NCT00449865.

Resumen vía Europe PMC. Los derechos de autor siguen siendo de los autores o la editorial.

Confianza de la comunidad

Cargando…

¿Cuánto confías en los hallazgos de este estudio?

0 · nada10 · totalmente

Comentarios

¿Algo está mal aquí?

Señala este estudio si su información, etiquetas o financiación parecen incorrectas. Un editor revisa cada señalamiento.

Información educativa sobre investigación publicada. No es consejo médico ni una recomendación para empezar o dejar nada.