Project among African-Americans to explore risks for schizophrenia (PAARTNERS): Recruitment and assessment methods

被引:31
作者
Aliyu, Muktar H.
Calkins, Monica E.
Swanson, Charlie L., Jr.
Lyons, Paul D.
Savage, Robert M.
May, Roberta
Wiener, Howard
Devlin, Bernie
Nimgaonkar, Vishwajit L.
Ragland, J. Daniel
Gur, Raquel E.
Gur, Ruben C.
Bradford, L. Dianne
Edwards, Neil
Kwentus, Joseph
McEvoy, Joseph P.
Santos, Alberto B.
McCleod-Bryant, Stephen
Tennison, Clifton
Go, Rodney C. P.
机构
[1] Univ Alabama, Dept Psychiat, Birmingham, AL 35294 USA
[2] Univ Penn, Dept Psychiat, Neuropsychiat Sect, Philadelphia, PA 19104 USA
[3] Univ Virginia, Dept Neurol, Charlottesville, VA USA
[4] Univ Alabama, Dept Epidemiol, Birmingham, AL 35294 USA
[5] Univ Pittsburgh, Sch Med, Dept Psychiat, Pittsburgh, PA USA
[6] Morehouse Sch Med, Dept Psychiat, Atlanta, GA 30310 USA
[7] Univ Tennessee, Coll Med, Dept Psychiat, Memphis, TN USA
[8] Univ Mississippi, Med Ctr, Dept Psychiat & Human Behav, Jackson, MS 39216 USA
[9] Duke Univ, Med Ctr, John Umstead Hosp, Butner, NC USA
[10] Med Univ S Carolina, Dept Psychiat & Behav Sci, Charleston, SC 29425 USA
[11] Helsn Ross McNabb Ctr, Knoxville, TN USA
关键词
schizophrenia; genetics; endophenotype; neurocognitive; African-American;
D O I
10.1016/j.schres.2006.06.027
中图分类号
R749 [精神病学];
学科分类号
100205 [精神病与精神卫生学];
摘要
The Project among Aftican-Americans to Explore Risks for Schizophrenia (PAARTNERS) is a multi-site, NIMH-funded study that seeks to identify genetic polymorphisms that confer susceptibility to schizophrenia among African-Americans by linkage mapping and targeted association analyses. Because deficits in certain dimensions of cognitive ability are thought to underlie liability to schizophrenia, the project also examines cognitive abilities in individuals affected by schizophrenia and their extended family members. This article describes PAARTNERS study design, ascertainment methods and preliminary sample characteristics. We aim to recruit a sample of 1260 African-American families, all of whom have at least one proband with schizophrenia or schizoaffective disorder. The data collection protocol includes a structured Diagnostic Interview for Genetic Studies, Family Interview for Genetic Studies, focused neurocognitive assessment, medical records review, and the collection of blood or buccal cells for genetic analyses. We have currently completed study procedures for 106 affected sib-pair, 457 case-parent trio and 23 multiplex families. A total of 289 probands have completed the best estimate final diagnosis process and 1153 probands and family members have been administered the computerized neuropsychological battery. This project lays the foundation for future analysis of cognitive and behavioral endophenotypes. This novel integration of diagnostic, neurocognitive and genetic data will also generate valuable information for future phenotypic and genetic studies of schizophrenia. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:32 / 44
页数:13
相关论文
共 77 条
[1]
Handling marker-marker linkage disequilibrium: Pedigree analysis with clustered markers [J].
Abecasis, GR ;
Wigginton, JE .
AMERICAN JOURNAL OF HUMAN GENETICS, 2005, 77 (05) :754-767
[2]
Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1 [J].
Abecasis, GR ;
Burt, RA ;
Hall, D ;
Bochum, S ;
Doheny, KF ;
Lundy, SL ;
Torrington, M ;
Roos, JL ;
Gogos, JA ;
Karayiorgou, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (03) :403-417
[3]
Almasy L, 1997, GENET EPIDEMIOL, V14, P953, DOI 10.1002/(SICI)1098-2272(1997)14:6<953::AID-GEPI65>3.0.CO
[4]
2-K
[5]
Multipoint quantitative-trait linkage analysis in general pedigrees [J].
Almasy, L ;
Blangero, J .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (05) :1198-1211
[6]
AMOS CI, 1990, AM J HUM GENET, V47, P247
[7]
A COMPARISON OF UNIVARIATE AND MULTIVARIATE TESTS FOR GENETIC-LINKAGE [J].
AMOS, CI ;
LAING, AE .
GENETIC EPIDEMIOLOGY, 1993, 10 (06) :671-676
[8]
[Anonymous], 2000, DIAGN STAT MAN MENT
[9]
Linkage analysis of anorexia and bulimia nervosa cohorts using selected behavioral phenotypes as quantitative traits or covariates [J].
Bacanu, SA ;
Bulik, CM ;
Klump, K ;
Fichter, MM ;
Halmi, KA ;
Keel, P ;
Kaplan, AS ;
Mitchell, JE ;
Rotondo, A ;
Strober, M ;
Treasure, J ;
Woodside, DB ;
Sonpar, VA ;
Xie, WT ;
Bergen, AW ;
Berrettini, WH ;
Kaye, WH ;
Devlin, B .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2005, 139B (01) :61-68
[10]
Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia [J].
Badner, JA ;
Gershon, ES .
MOLECULAR PSYCHIATRY, 2002, 7 (04) :405-411