TY - JOUR
T1 - Patterns of DSM-III-R alcohol dependence symptom progression in a general population survey
AU - Nelson, C. B.
AU - Little, R. J.A.
AU - Heath, A. C.
AU - Kessler, R. C.
N1 - Funding Information:
The NCS is a collaborative epidemiological investigation of the prevalence, causes, and consequences of psychiatric morbidity and co-morbidity in the United States supported by the National Institute of Mental Health (Grants MH46376 and MH49098) with supplemental support from the National Institute of Drug Abuse (through a supplement to MH46376) and the W. T. Grant Foundation (Grant 90135190). Ronald C. Kessler is the Principal Investigator. Collaborating NCS sites and investigators are: the Addiction Research Foundation (Robin Room), Duke University Medical Center (Dan Blazer, Marvin Swartz), Harvard University (Richard Frank), Johns Hopkins University (James Anthony, William Eaton, Philip Leaf), the Max Planck Institute of Psychiatry -Clinical Institute (Hans-Ulrich Wittchen), the Medical College of Virginia (Kenneth Kendler), the University of Michigan (Lloyd Johnston, Ronald Kessler, Roderick Little), New York University (Patrick Shrout) SUNY Stony Brook (Evelyn Bromet), the University of Toronto (R. Jay Turner), and Washington University School of Medicine (Linda Cottier, Andrew Heath). Preparation of this report was also supported by a Research Scientist Award to Kessler (Grant MH00507). A complete list of NCS publications can be obtained from the NCS Study Coordinator, Room 1006, Institute for Social Research, the University of Michigan, Box 1248, Ann Arbor, MI 48106-1248, USA. The full text of this paper along with all other NCS publications, study documentation, and interview schedules can be obtained directly via the Internet by completing the following steps: FTP 141.211.207.206; NAME = anonymous; PASSWORD = (your Internet e-mail address); read the INSTRUCTIONS file for details about how to upload the NCS documents.
PY - 1996/5
Y1 - 1996/5
N2 - Age of onset reports obtained retrospectively for each symptom of DSM-III-R alcohol dependence (AD) are used to study patterns of lifetime symptom progression in a large general-population survey of people in the United States. It is shown that symptom progression among a substantial majority of respondents can be summarized as movement across three clusters. Cluster A is defined by symptoms of role impairment/hazardous use (A4), use despite social, psychological or physical problems (A6), and drinking larger amounts or over a longer period of time than intended (A1). Cluster B is defined by tolerance (A7) and impaired control (A2, A3). Cluster C is defined by withdrawal (A8, A9) and giving up activities in order to drink (A5). Clusters are shown to follow a time sequence, with at least one symptom in Cluster A usually occurring first, followed by symptoms in Clusters B and C. In all, 83.4% of the symptom cluster transitions estimated from retrospective age of onset reports are consistent with this progression. Progression to AD is differentially predicted by symptom profiles reported at the age of first symptom onset, with persons reporting Cluster C symptoms most likely to progress subsequently to AD. Furthermore, profiles of AD defined by the highest symptom cluster present at AD onset are differentially predicted by prior personal and parental histories of psychopathology and, among men, are predictive of diagnosis persistence.
AB - Age of onset reports obtained retrospectively for each symptom of DSM-III-R alcohol dependence (AD) are used to study patterns of lifetime symptom progression in a large general-population survey of people in the United States. It is shown that symptom progression among a substantial majority of respondents can be summarized as movement across three clusters. Cluster A is defined by symptoms of role impairment/hazardous use (A4), use despite social, psychological or physical problems (A6), and drinking larger amounts or over a longer period of time than intended (A1). Cluster B is defined by tolerance (A7) and impaired control (A2, A3). Cluster C is defined by withdrawal (A8, A9) and giving up activities in order to drink (A5). Clusters are shown to follow a time sequence, with at least one symptom in Cluster A usually occurring first, followed by symptoms in Clusters B and C. In all, 83.4% of the symptom cluster transitions estimated from retrospective age of onset reports are consistent with this progression. Progression to AD is differentially predicted by symptom profiles reported at the age of first symptom onset, with persons reporting Cluster C symptoms most likely to progress subsequently to AD. Furthermore, profiles of AD defined by the highest symptom cluster present at AD onset are differentially predicted by prior personal and parental histories of psychopathology and, among men, are predictive of diagnosis persistence.
UR - http://www.scopus.com/inward/record.url?scp=0029923820&partnerID=8YFLogxK
U2 - 10.1017/s0033291700035534
DO - 10.1017/s0033291700035534
M3 - Article
C2 - 8733204
AN - SCOPUS:0029923820
SN - 0033-2917
VL - 26
SP - 449
EP - 460
JO - Psychological medicine
JF - Psychological medicine
IS - 3
ER -