TY - JOUR
T1 - Evidence of Familial Association Between Attention Deficit Disorder and Major Affective Disorders
AU - Biederman, Joseph
AU - Faraone, Stephen V.
AU - Keenan, Kate
AU - Tsuang, Ming T.
PY - 1991/7
Y1 - 1991/7
N2 - • With the use of family study methods and assessments by “blinded” raters, we tested hypotheses about patterns of familial association between DSM-III attention deficit disorder (ADD) and affective disorders (AFFs) among first-degree relatives of clinically referred children and adolescents with ADD (73 probands, 264 relatives) and normal controls (26 probands, 92 relatives). Among the 73 ADD probands, 24 (33%) met criteria for AFFs (major depression, n = 15 [21%]; bipolar disorder, n = 8 [11%]; and dysthymia, n = 1 [1%]). After stratification of the ADD sample into those with AFFs (ADD+AFF) and those without AFF (ADD), familial risk analyses revealed the following: (1) the relatives of each ADD proband subgroup were at significantly greater risk for ADD than were relatives of normal controls; (2) the agecorrected morbidity risk for ADD was not significantly different between relatives of ADD and ADD+AFF (27% vs 22%); however, these two risks were significantly greater than the risk to relatives of normal controls (5%); (3) the risk for any AFF (bipolar disorder, major depressive disorder, or dysthymia) was not significantly different between relatives of ADD probands and ADD+AFF probands (28% and 25%), but these two risks were significantly greater than the risk to relatives of normal controls (4%); (4) ADD and AFFs did not cosegregate within families; and (5) there was no evidence for nonrandom mating. These findings are consistent with the hypothesis that ADD and AFFs may share common familial vulnerabilities.
AB - • With the use of family study methods and assessments by “blinded” raters, we tested hypotheses about patterns of familial association between DSM-III attention deficit disorder (ADD) and affective disorders (AFFs) among first-degree relatives of clinically referred children and adolescents with ADD (73 probands, 264 relatives) and normal controls (26 probands, 92 relatives). Among the 73 ADD probands, 24 (33%) met criteria for AFFs (major depression, n = 15 [21%]; bipolar disorder, n = 8 [11%]; and dysthymia, n = 1 [1%]). After stratification of the ADD sample into those with AFFs (ADD+AFF) and those without AFF (ADD), familial risk analyses revealed the following: (1) the relatives of each ADD proband subgroup were at significantly greater risk for ADD than were relatives of normal controls; (2) the agecorrected morbidity risk for ADD was not significantly different between relatives of ADD and ADD+AFF (27% vs 22%); however, these two risks were significantly greater than the risk to relatives of normal controls (5%); (3) the risk for any AFF (bipolar disorder, major depressive disorder, or dysthymia) was not significantly different between relatives of ADD probands and ADD+AFF probands (28% and 25%), but these two risks were significantly greater than the risk to relatives of normal controls (4%); (4) ADD and AFFs did not cosegregate within families; and (5) there was no evidence for nonrandom mating. These findings are consistent with the hypothesis that ADD and AFFs may share common familial vulnerabilities.
UR - http://www.scopus.com/inward/record.url?scp=0025783964&partnerID=8YFLogxK
U2 - 10.1001/archpsyc.1991.01810310051009
DO - 10.1001/archpsyc.1991.01810310051009
M3 - Article
C2 - 2069494
AN - SCOPUS:0025783964
SN - 0003-990X
VL - 48
SP - 633
EP - 642
JO - Archives of General Psychiatry
JF - Archives of General Psychiatry
IS - 7
ER -