TY - JOUR
T1 - A unified approach of meta-analysis
T2 - Application to an antecedent biomarker study in Alzheimer's disease
AU - Xiong, Chengjie
AU - van Belle, Gerald
AU - Zhu, Kejun
AU - Miller, J. Philip
AU - Morris, John C.
N1 - Funding Information:
The authors would like to thank Dr. David Holtzman and Dr.Anne Fagan, Department of Neurology,Washington University in St. Louis, for providing the biomarker data used in the paper. The authors also thank the Clinical and Psychometric and Genetic Cores of the Alzheimer’s Disease Research Center at Washington University for subject assessments. Dr. Xiong’s work was supported by grant K25 AG025189 from the National Institute on Aging and by the Alan A. and Edith Wolff CharitableTrust. Financial support for this study was also provided in part by National Institute onAging grantsAG003991, AG005681, and AG026276 for Chengjie Xiong, J. Philip Miller, and John C. Morris. SAS code for implementing the proposed methodology can be requested to the corresponding author through email at [email protected].
PY - 2011/1
Y1 - 2011/1
N2 - This article provides a unified methodology of meta-analysis that synthesizes medical evidence by using both available individual patient data (IPD) and published summary statistics within the framework of likelihood principle. Most up-to-date scientific evidence on medicine is crucial information not only to consumers but also to decision makers, and can only be obtained when existing evidence from the literature and the most recent IPD are optimally synthesized. We propose a general linear mixed effects model to conduct meta-analyses when IPD are only available for some of the studies and summary statistics have to be used for the rest of the studies. Our approach includes both the traditional meta-analyses in which only summary statistics are available for all studies and the other extreme case in which IPD are available for all studies as special examples. We implement the proposed model with statistical procedures from standard computing packages. We provide measures of heterogeneity based on the proposed model. Finally, we demonstrate the proposed methodology through a real-life example by studying the cerebrospinal fluid biomarkers to identify individuals with a high risk of developing Alzheimer's disease when they are still cognitively normal.
AB - This article provides a unified methodology of meta-analysis that synthesizes medical evidence by using both available individual patient data (IPD) and published summary statistics within the framework of likelihood principle. Most up-to-date scientific evidence on medicine is crucial information not only to consumers but also to decision makers, and can only be obtained when existing evidence from the literature and the most recent IPD are optimally synthesized. We propose a general linear mixed effects model to conduct meta-analyses when IPD are only available for some of the studies and summary statistics have to be used for the rest of the studies. Our approach includes both the traditional meta-analyses in which only summary statistics are available for all studies and the other extreme case in which IPD are available for all studies as special examples. We implement the proposed model with statistical procedures from standard computing packages. We provide measures of heterogeneity based on the proposed model. Finally, we demonstrate the proposed methodology through a real-life example by studying the cerebrospinal fluid biomarkers to identify individuals with a high risk of developing Alzheimer's disease when they are still cognitively normal.
KW - Confidence interval
KW - General linear mixed effects model
KW - Heterogeneity index
KW - Individual patient data
KW - Maximum likelihood estimate (MLE)
KW - Meta-analyses
UR - http://www.scopus.com/inward/record.url?scp=78650050375&partnerID=8YFLogxK
U2 - 10.1080/02664760903008987
DO - 10.1080/02664760903008987
M3 - Article
C2 - 21221414
AN - SCOPUS:78650050375
SN - 0266-4763
VL - 38
SP - 15
EP - 27
JO - Journal of Applied Statistics
JF - Journal of Applied Statistics
IS - 1
ER -