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

被引:31
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 71 条
  • [1] Prevalence of psychiatric disorders across Latino subgroups in the United States
    Alegria, Margarita
    Mulvaney-Day, Norah
    Torres, Maria
    Polo, Antonio
    Cao, Zhun
    Canino, Glorisa
    [J]. AMERICAN JOURNAL OF PUBLIC HEALTH, 2007, 97 (01) : 68 - 75
  • [2] Differential resting quantitive electroencephalographic alpha patterns in women with environmental chemical intolerance, depressives, and normals
    Bell, IR
    Schwartz, GE
    Hardin, EE
    Baldwin, CM
    Kline, JP
    [J]. BIOLOGICAL PSYCHIATRY, 1998, 43 (05) : 376 - 388
  • [3] Regional brain asymmetries in major depression with or without an anxiety disorder: A quantitative electroencephalographic study
    Bruder, GE
    Fong, R
    Tenke, CE
    Leite, P
    Towey, JP
    Stewart, JE
    McGrath, PJ
    Quitkin, FM
    [J]. BIOLOGICAL PSYCHIATRY, 1997, 41 (09) : 939 - 948
  • [4] Electroencephalographic measures of regional hemispheric activity in offspring at risk for depressive disorders
    Bruder, GE
    Tenke, CE
    Warner, V
    Nomura, Y
    Grillon, C
    Hille, J
    Leite, P
    Weissman, MM
    [J]. BIOLOGICAL PSYCHIATRY, 2005, 57 (04) : 328 - 335
  • [5] CEREBRAL LATERALITY AND DEPRESSION - DIFFERENCES IN PERCEPTUAL ASYMMETRY AMONG DIAGNOSTIC SUBTYPES
    BRUDER, GE
    QUITKIN, FM
    STEWART, JW
    MARTIN, C
    VOGLMAIER, MM
    HARRISON, WM
    [J]. JOURNAL OF ABNORMAL PSYCHOLOGY, 1989, 98 (02) : 177 - 186
  • [6] Grandchildren at high and low risk for depression differ in EEG measures of regional brain asymmetry
    Bruder, Gerard E.
    Tenke, Craig E.
    Warner, Virginia
    Weissman, Myrna M.
    [J]. BIOLOGICAL PSYCHIATRY, 2007, 62 (11) : 1317 - 1323
  • [7] Relationship of resting EEG with anatomical MRI measures in individuals at high and low risk for depression
    Bruder, Gerard E.
    Bansal, Ravi
    Tenke, Craig E.
    Liu, Jun
    Hao, Xuejun
    Warner, Virginia
    Peterson, Bradley S.
    Weissman, Myrna M.
    [J]. HUMAN BRAIN MAPPING, 2012, 33 (06) : 1325 - 1333
  • [8] A randomized trial of a group cognitive intervention for preventing depression in adolescent offspring of depressed parents
    Clarke, GN
    Hornbrook, M
    Lynch, F
    Polen, M
    Gale, J
    Beardslee, W
    O'Connor, E
    Seeley, J
    [J]. ARCHIVES OF GENERAL PSYCHIATRY, 2001, 58 (12) : 1127 - 1134
  • [9] Association of the 5-HTTLPR genotype and unipolar depression: a meta-analysis
    Clarke, H.
    Flint, J.
    Attwood, A. S.
    Munafo, M. R.
    [J]. PSYCHOLOGICAL MEDICINE, 2010, 40 (11) : 1767 - 1778
  • [10] A longitudinal look at the relation between depression and anxiety in children and adolescents
    Cole, DA
    Peeke, LG
    Martin, JM
    Truglio, R
    Seroczynski, AD
    [J]. JOURNAL OF CONSULTING AND CLINICAL PSYCHOLOGY, 1998, 66 (03) : 451 - 460