Malignancy of recurrent, early-onset major depression: A family study

被引:61
作者
Zubenko, GS
Zubenko, WN
Spiker, DG
Giles, DE
Kaplan, BB
机构
[1] Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA 15261 USA
[2] Carnegie Mellon Univ, Mellon Coll Sci, Dept Biol Sci, Pittsburgh, PA 15213 USA
[3] Univ Rochester, Sch Med, Dept Psychiat, Rochester, NY 14642 USA
[4] Univ Rochester, Sch Med, Dept Neurol, Rochester, NY 14642 USA
[5] NIMH, Intramural Res Program, Bethesda, MD 20892 USA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 2001年 / 105卷 / 08期
关键词
major depression; recurrent mood disorders; comorbidity; mortality; family and genetic studies;
D O I
10.1002/ajmg.1554
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Coordinated efforts to identify susceptibility genes for unipolar major depressive disorder (MDD) and related disorders are now underway. These studies have focused on recurrent, early-onset MDD (RE-MDD), the most heritable form of this disorder. The goal of this study was to characterize the burden of MDD and other mood disorders, comorbid mental disorders, and excess mortality in RE-MDD families. A total of 81 families were identified through probands over the age of 18, who met criteria for recurrent (greater than or equal to2 episodes), early-onset (less than or equal to 25 years), nonpsychotic, unipolar MDD (RE-MDD), and included 407 first-degree relatives and 835 extended relatives. Psychiatric diagnoses for probands and their family members who provided blood samples were formulated from structured personal interviews, structured family history assessments, and available medical records. The remaining family members who participated and those who were deceased were evaluated through the family history method augmented by available medical records. Best estimate diagnoses were made during a consensus conference according to established diagnostic criteria. Approximately half of the first-degree relatives and a quarter of extended relatives of RE-MDD probands suffered from at least one mood disorder, typically MDD. As commonly observed for other oligogenic, multifactorial disorders, the severity of MMD reflected by age at onset and number of episodes attenuated with increasing familial/genetic distance from the proband. A substantial fraction of RE-MDD probands and their first-degree relatives met diagnostic criteria for additional psychiatric disorders that include prominent disturbances of mood. The deceased relatives of RE-MDD probands died at a median age that was 8 years earlier than for the local population; over 40% died before reaching age 65. These differences in mortality statistics resulted from a shift toward younger ages at death across the lifespan, including a fivefold increase in the proportion of individuals who died in the first year of life. Several-fold increases in the proportion of deaths by suicide, homicide, and liver disease were observed among the relatives of RE-MDD probands. However, the rank order of the three most common causes of death-heart disease, cancer, and stroke-remained unchanged and differences in the proportions of deaths from the remaining causes were small. RE-MDD is a strongly familial condition with a high rate of psychiatric comorbidity, whose malignant effects have a significant negative impact on the health and longevity of patients and their family members. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:690 / 699
页数:10
相关论文
共 66 条
[1]  
*ALL HLTH DEP, 1999, ALL COUNT MORT STAT, P1
[2]  
ANDREASEN NC, 1986, ARCH GEN PSYCHIAT, V43, P421
[3]  
Angst J, 1999, J CLIN PSYCHIAT, V60, P57
[4]  
[Anonymous], 1980, SCHEDULE AFFECTIVE D
[5]  
[Anonymous], 1999, MENT HLTH REP SURG G
[6]  
AVERY D, 1976, ARCH GEN PSYCHIAT, V33, P1029
[7]  
Barbee J G, 1998, Ann Clin Psychiatry, V10, P15, DOI 10.3109/10401239809148814
[8]   SCHIZOAFFECTIVE ILLNESS, SCHIZOPHRENIA AND AFFECTIVE-DISORDERS - MORBIDITY RISK AND GENETIC TRANSMISSION [J].
BARON, M ;
GRUEN, R ;
ASNIS, L ;
KANE, J .
ACTA PSYCHIATRICA SCANDINAVICA, 1982, 65 (04) :253-262
[9]   Susceptibility loci for bipolar disorder: Overlap with inherited vulnerability to schizophrenia [J].
Berrettini, WH .
BIOLOGICAL PSYCHIATRY, 2000, 47 (03) :245-251
[10]  
BLAND RC, 1986, ARCH GEN PSYCHIAT, V43, P1085