Using the high-risk family design to identify biomarkers for major depression

被引:30
|
作者
Talati, Ardesheer [1 ,2 ]
Weissman, Myrna M. [1 ,2 ,3 ]
Hamilton, Steven P. [4 ]
机构
[1] Columbia Univ Coll Phys & Surg, Dept Psychiat, New York, NY 10032 USA
[2] New York State Psychiat Inst & Hosp, Div Epidemiol, New York, NY 10032 USA
[3] Columbia Univ, Dept Epidemiol, Mailman Sch Publ Hlth, New York, NY 10032 USA
[4] Univ Calif San Francisco, Dept Psychiat, Inst Human Genet, San Francisco, CA 94143 USA
关键词
major depressive disorder; high-risk electroencephalography; imaging; genetics; endophenotype; MENTAL-DISORDERS; UNIPOLAR DEPRESSION; QUANTITATIVE EEG; EARLY-ADULTHOOD; BRAIN ACTIVITY; ANXIETY; ONSET; ASYMMETRY; CHILDREN; PSYCHOPATHOLOGY;
D O I
10.1098/rstb.2012.0129
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The familial nature of major depressive disorder (MDD) is now well recognized. We followed children and grandchildren of probands with and without MDD to examine transmission of depression over generations, and to identify early vulnerability markers prior to the onset of disease. The study now includes three generations and five completed assessment waves spanning 25 years, with a sixth wave underway. Beginning with the fourth wave, we collected measures of brain structure (magnetic resonance imaging, MRI) and physiology (electroencephalography, EEG) and DNA in order to examine at a biological level why the offspring of depressed parents were at higher risk. In this paper, we provide an overview of the study design, the main findings, including new data, and the role of the high-risk design in translational research. We demonstrate that offspring of depressed parents ('high-risk'), when compared with those of non-depressed parents ('low-risk'), were at increased risk for depressive and anxiety disorders, with anxiety appearing earlier and being a predisposing factor for MDD. Offspring with two generations previously affected were at greatest risk. Thinning of the cortical mantle (MRI) and reduced resting-state activity (EEG) within the right parieto-temporal hemisphere differentiated high- from low-risk offspring, regardless of whether the offspring had MDD, suggesting that these measures might serve as familial trait markers for depression and related syndromes. The high- and low-risk offspring also differed by serotonin transporter promoter length polymorphism genotypes, even though the same genotypes were not associated with the presence of MDD. The high-risk epidemiological design appears to be a particularly valuable asset in translational research as it allows targeting of biological processes that emerge prior to the onset of disease, and identifies individuals at high risk for the disorder who may carry the trait or marker but not yet be affected.
引用
收藏
页数:10
相关论文
共 50 条
  • [41] MRI in children at high risk for major depression
    Peterson, B
    Zhu, HT
    Bansal, R
    Weissman, M
    NEUROPSYCHOPHARMACOLOGY, 2004, 29 : S5 - S5
  • [42] THREE GENERATIONS AT HIGH-RISK AND LOW-RISK FOR DEPRESSION
    Weissman, Myrna M.
    JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 2016, 55 (10): : S306 - S306
  • [43] Common Heritable Contributions to Low-Risk Trauma, High-Risk Trauma, Posttraumatic Stress Disorder, and Major Depression
    Sartor, Carolyn E.
    Grant, Julia D.
    Lynskey, Michael T.
    McCutcheon, Vivia V.
    Waldron, Mary
    Statham, Dixie J.
    Bucholz, Kathleen K.
    Madden, Pamela A. F.
    Heath, Andrew C.
    Martin, Nicholas G.
    Nelson, Elliot C.
    ARCHIVES OF GENERAL PSYCHIATRY, 2012, 69 (03) : 293 - 299
  • [44] PRELIMINARY-STUDY TO IDENTIFY CANCER-PATIENTS AT HIGH-RISK OF VENOUS THROMBOSIS FOLLOWING MAJOR SURGERY
    FALANGA, A
    OFOSU, FA
    CORTELAZZO, S
    DELAINI, F
    CONSONNI, R
    CACCIA, R
    LONGATTI, S
    MARAN, D
    RODEGHIERO, F
    POGLIANI, E
    MARASSI, A
    DANGELO, A
    BARBUI, T
    BRITISH JOURNAL OF HAEMATOLOGY, 1993, 85 (04) : 745 - 750
  • [45] FAMILY ENVIRONMENT AND THE DEVELOPMENT OF HIGH-RISK CHILDREN
    PETERANDER, F
    HEILPADAGOGISCHE FORSCHUNG, 1988, 14 (03): : 170 - 179
  • [46] Family relations and high-risk behavior of adolescents
    Brand, G
    Millot, JL
    INTERNATIONAL JOURNAL OF PSYCHOLOGY, 2000, 35 (3-4) : 376 - 376
  • [47] Family relations and high-risk behaviour of adolescents
    Oubrayrie, NMA
    Safont-Mottay, C
    INTERNATIONAL JOURNAL OF PSYCHOLOGY, 2000, 35 (3-4) : 11 - 11
  • [48] Genomic analysis in active surveillance: predicting high-risk disease using tissue biomarkers
    Donovan, Michael J.
    Cordon-Cardo, Carlos
    CURRENT OPINION IN UROLOGY, 2014, 24 (03) : 303 - 310
  • [49] Using a cognitive endophenotype to identify risk genes for depression
    Haeffel, Gerald J.
    Eastman, Maria
    Grigorenko, Elena L.
    NEUROSCIENCE LETTERS, 2012, 510 (01) : 10 - 13
  • [50] Functional Connectivity Biomarkers of Emotion Regulation That Distinguish Risk for Bipolar Versus Unipolar Depression in Clinically Asymptomatic High-Risk Youth
    Fischer, Adina
    Nimarko, Akua
    Hagan, Kelsey
    Gotlib, Ian
    Singh, Manpreet
    NEUROPSYCHOPHARMACOLOGY, 2019, 44 (SUPPL 1) : 434 - 435