The familial transmission of primary major depressive disorder. 1987

T Reich, and P Van Eerdewegh, and J Rice, and J Mullaney, and J Endicott, and G L Klerman
Department of Psychiatry, Washington University, St. Louis, Missouri.

This is a study of the familial transmission of Primary Major Depressive Disorder in the families of 235 probands with this disorder ascertained as part of the NIMH-CRB Collaborative Depression Program. Eight hundred and twenty-six interviewed first degree relatives and 109 spouses are included. Research Diagnostic Criteria have been used and interviews were done using the SADS-L schedule. Prior analyses of these data have established the presence of strong secular trends in the age-of-onset and prevalence of Major Depressive Disorder in these families. Accordingly, new methods for the analysis of family data which incorporate secular variation were developed. Non-parametric Survival Analysis, using the Cox Proportional Hazards Model, guided the formulation of a quantitative family transmission model. Then a family analysis was conducted with the Multifactorial Model of Disease Transmission and the Tau Path Analytic Model. Using the non-parametric approach, only the sibs birth cohort, sex and affectational status of the mother were significantly related to the time of onset of illness in siblings. Proband sex, age-of-onset, and the presence of illness in the father were not significant. The quantitative analysis confirmed that more recently born cohorts of individuals had an increased expected lifetime prevalence and a decreased age-of-onset of Primary Major Depressive Disorder. Assortative mating was present and environmental factors common to siblings did not make a significant contribution to the phenotypic variance. Sex specific transmissibilities were found and the transmissibility in females (t2 = 0.62) was significantly greater than that of males (t2 = 0.28). There was a trend for the transmissibility of Primary Major Disorder to be greater in more recently born cohorts.

UI MeSH Term Description Entries
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D010641 Phenotype The outward appearance of the individual. It is the product of interactions between genes, and between the GENOTYPE and the environment. Phenotypes
D003866 Depressive Disorder An affective disorder manifested by either a dysphoric mood or loss of interest or pleasure in usual activities. The mood disturbance is prominent and relatively persistent. Depression, Endogenous,Depression, Neurotic,Depression, Unipolar,Depressive Syndrome,Melancholia,Neurosis, Depressive,Unipolar Depression,Depressions, Endogenous,Depressions, Neurotic,Depressions, Unipolar,Depressive Disorders,Depressive Neuroses,Depressive Neurosis,Depressive Syndromes,Disorder, Depressive,Disorders, Depressive,Endogenous Depression,Endogenous Depressions,Melancholias,Neuroses, Depressive,Neurotic Depression,Neurotic Depressions,Syndrome, Depressive,Syndromes, Depressive,Unipolar Depressions
D005787 Gene Frequency The proportion of one particular in the total of all ALLELES for one genetic locus in a breeding POPULATION. Allele Frequency,Genetic Equilibrium,Equilibrium, Genetic,Allele Frequencies,Frequencies, Allele,Frequencies, Gene,Frequency, Allele,Frequency, Gene,Gene Frequencies
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D000367 Age Factors Age as a constituent element or influence contributing to the production of a result. It may be applicable to the cause or the effect of a circumstance. It is used with human or animal concepts but should be differentiated from AGING, a physiological process, and TIME FACTORS which refers only to the passage of time. Age Reporting,Age Factor,Factor, Age,Factors, Age
D012307 Risk Factors An aspect of personal behavior or lifestyle, environmental exposure, inborn or inherited characteristic, which, based on epidemiological evidence, is known to be associated with a health-related condition considered important to prevent. Health Correlates,Risk Factor Scores,Risk Scores,Social Risk Factors,Population at Risk,Populations at Risk,Correlates, Health,Factor, Risk,Factor, Social Risk,Factors, Social Risk,Risk Factor,Risk Factor Score,Risk Factor, Social,Risk Factors, Social,Risk Score,Score, Risk,Score, Risk Factor,Social Risk Factor

Related Publications

T Reich, and P Van Eerdewegh, and J Rice, and J Mullaney, and J Endicott, and G L Klerman
February 1991, The American journal of psychiatry,
T Reich, and P Van Eerdewegh, and J Rice, and J Mullaney, and J Endicott, and G L Klerman
March 2012, Genetics in medicine : official journal of the American College of Medical Genetics,
T Reich, and P Van Eerdewegh, and J Rice, and J Mullaney, and J Endicott, and G L Klerman
June 1990, Journal of affective disorders,
T Reich, and P Van Eerdewegh, and J Rice, and J Mullaney, and J Endicott, and G L Klerman
January 2008, Michigan medicine,
T Reich, and P Van Eerdewegh, and J Rice, and J Mullaney, and J Endicott, and G L Klerman
January 1994, Anxiety,
T Reich, and P Van Eerdewegh, and J Rice, and J Mullaney, and J Endicott, and G L Klerman
July 2018, Depression and anxiety,
T Reich, and P Van Eerdewegh, and J Rice, and J Mullaney, and J Endicott, and G L Klerman
January 1993, The Journal of the American Board of Family Practice,
T Reich, and P Van Eerdewegh, and J Rice, and J Mullaney, and J Endicott, and G L Klerman
April 2005, The Journal of clinical psychiatry,
T Reich, and P Van Eerdewegh, and J Rice, and J Mullaney, and J Endicott, and G L Klerman
April 2008, The New England journal of medicine,
T Reich, and P Van Eerdewegh, and J Rice, and J Mullaney, and J Endicott, and G L Klerman
January 2005, Current pharmaceutical design,
Copied contents to your clipboard!