TY - JOUR
T1 - ALS Multicenter Cohort Study of Oxidative Stress (ALS COSMOS)
T2 - Study methodology, recruitment, and baseline demographic and disease characteristics
AU - Mitsumoto, Hiroshi
AU - Factor-Litvak, Pam
AU - Andrews, Howard
AU - Goetz, Raymond R.
AU - Andrews, Leslie
AU - Rabkin, Judith G.
AU - Mcelhiney, Martin
AU - Nieves, Jeri
AU - Santella, Regina M.
AU - Murphy, Jennifer
AU - Hupf, Jonathan
AU - Singleton, Jess
AU - Merle, David
AU - Kilty, Mary
AU - Heitzman, Daragh
AU - Bedlack, Richard S.
AU - Miller, Robert G.
AU - Katz, Jonathan S.
AU - Forshew, Dallas
AU - Barohn, Richard J.
AU - Sorenson, Eric J.
AU - Oskarsson, Bjorn
AU - Fernandes Filho, J. Americo M.
AU - Kasarskis, Edward J.
AU - Lomen-Hoerth, Catherine
AU - Mozaffar, Tahseen
AU - Rollins, Yvonne D.
AU - Nations, Sharon P.
AU - Swenson, Andrea J.
AU - Shefner, Jeremy M.
AU - Andrews, Jinsy A.
AU - Koczon-Jaremko, Boguslawa A.
PY - 2014/6
Y1 - 2014/6
N2 - In a multicenter study of newly diagnosed ALS patients without a reported family history of ALS, we are prospectively investigating whether markers of oxidative stress (OS) are associated with disease progression. Methods utilize an extensive structured telephone interview ascertaining environmental, lifestyle, dietary and psychological risk factors associated with OS. Detailed assessments were performed at baseline and at 3-6 month intervals during the ensuing 30 months. Our biorepository includes DNA, plasma, urine, and skin. Three hundred and fifty-five patients were recruited. Subjects were enrolled over a 36-month period at 16 sites. To meet the target number of subjects, the recruitment period was prolonged and additional sites were included. Results showed that demographic and disease characteristics were similar between 477 eligible/non-enrolled and enrolled patients, the only difference being type of health insurance among enrolled patients. Sites were divided into three groups by the number of enrolled subjects. Comparing these three groups, the Columbia site had fewer 'definite ALS' diagnoses. This is the first prospective, interdisciplinary, in-depth, multicenter epidemiological investigation of OS related to ALS progression and has been accomplished by an aggressive recruitment process. The baseline demographic and disease features of the study sample are now fully characterized.
AB - In a multicenter study of newly diagnosed ALS patients without a reported family history of ALS, we are prospectively investigating whether markers of oxidative stress (OS) are associated with disease progression. Methods utilize an extensive structured telephone interview ascertaining environmental, lifestyle, dietary and psychological risk factors associated with OS. Detailed assessments were performed at baseline and at 3-6 month intervals during the ensuing 30 months. Our biorepository includes DNA, plasma, urine, and skin. Three hundred and fifty-five patients were recruited. Subjects were enrolled over a 36-month period at 16 sites. To meet the target number of subjects, the recruitment period was prolonged and additional sites were included. Results showed that demographic and disease characteristics were similar between 477 eligible/non-enrolled and enrolled patients, the only difference being type of health insurance among enrolled patients. Sites were divided into three groups by the number of enrolled subjects. Comparing these three groups, the Columbia site had fewer 'definite ALS' diagnoses. This is the first prospective, interdisciplinary, in-depth, multicenter epidemiological investigation of OS related to ALS progression and has been accomplished by an aggressive recruitment process. The baseline demographic and disease features of the study sample are now fully characterized.
KW - ALS
KW - Disease progression
KW - Epidemiology
KW - Oxidative stress
KW - Survival
UR - http://www.scopus.com/inward/record.url?scp=84901494027&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84901494027&partnerID=8YFLogxK
U2 - 10.3109/21678421.2013.864312
DO - 10.3109/21678421.2013.864312
M3 - Article
C2 - 24564738
AN - SCOPUS:84901494027
SN - 2167-8421
VL - 15
SP - 192
EP - 203
JO - Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
JF - Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
IS - 3-4
ER -