What is chronic fatigue syndrome? Heterogeneity within an international multicentre study

被引:89
作者
Wilson, A
Hickie, I
Hadzi-Pavlovic, D
Wakefield, D
Parker, G
Straus, SE
Dale, J
McCluskey, D
Hinds, G
Brickman, A
Goldenberg, D
Demitrack, M
Blakely, T
Wessely, S
Sharpe, M
Lloyd, A
机构
[1] St George Hosp & Community Hlth Serv, Acad Dept Psychiat, Kogarah, NSW 2217, Australia
[2] Univ New S Wales, Sydney, NSW, Australia
[3] NIAID, Bethesda, MD 20892 USA
[4] Royal Victoria Hosp, Belfast BT12 6BA, Antrim, North Ireland
[5] Univ Miami, Coral Gables, FL 33124 USA
[6] Newton Wellesley Hosp, Arthrit Fibrositis Ctr, Boston, MA USA
[7] Univ Michigan, Ann Arbor, MI 48109 USA
[8] Kings Coll London, Sch Med, London WC2R 2LS, England
[9] Univ Edinburgh, Edinburgh, Midlothian, Scotland
关键词
chronic fatigue; somatization; latent class;
D O I
10.1046/j.1440-1614.2001.00888.x
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: We sought to compare the characteristics of patients presenting with chronic fatigue (CF) and related syndromes in eight international centres and to subclassify these subjects based on symptom profiles. The validity of the subclasses was then tested against clinical data. Method: Subjects with a clinical diagnosis of CF completed a 119-item self-report questionnaire to provide clinical symptom data and other information such as illness course and functional impairment. Subclasses were generated using a principal components-like analysis followed by latent profile analysis (LPA). Results: 744 subjects returned complete data sets (mean age 40.8 years, mean length of illness 7.9 years, female to male ratio 3:1). Overall, the subjects had a high rate of reporting typical CF symptoms (fatigue, neuropsychological dysfunction, sleep disturbance). Using LPA, two subclasses were generated. Class one (68% sample) was characterized by: younger age, lower female to male ratio; shorter episode duration; less premorbid, current and familial psychiatric morbidity; and, less functional disability. Class two subjects (32%) had features more consistent with a somatoform illness. There was substantial variation in subclass prevalences between the study centres (Class two range 6-48%). Conclusions: Criteria-based approaches to the diagnosis of CF and related syndromes do not select a homogeneous patient group. While substratification of patients is essential for further aetiological and treatment research, the basis for allocating such subcategories remains controversial.
引用
收藏
页码:520 / 527
页数:8
相关论文
共 28 条
[1]  
[Anonymous], 1987, DIAGNOSTIC STAT MANU, V4th
[2]  
Bartholomew DJ., 1987, LATENT VARIABLE MODE
[3]  
DAVIS JM, 1988, ARCH GEN PSYCHIAT, V45, P705
[4]   Is disabling fatigue in childhood influenced by genes? [J].
Farmer, A ;
Scourfield, J ;
Martin, N ;
Cardno, A ;
McGuffin, P .
PSYCHOLOGICAL MEDICINE, 1999, 29 (02) :279-282
[5]   THE CHRONIC FATIGUE SYNDROME - A COMPREHENSIVE APPROACH TO ITS DEFINITION AND STUDY [J].
FUKUDA, K ;
STRAUS, SE ;
HICKIE, I ;
SHARPE, MC ;
DOBBINS, JG ;
KOMAROFF, A ;
SCHLUEDERBERG, A ;
JONES, JF ;
LLOYD, AR ;
WESSELY, S ;
GANTZ, NM ;
HOLMES, GP ;
BUCHWALD, D ;
ABBEY, S ;
REST, J ;
LEVY, JA ;
JOLSON, H ;
PETERSON, DL ;
VERCOULEN, JHMM ;
TIRELLI, U ;
EVENGARD, B ;
NATELSON, BH ;
STEELE, L ;
REYES, M ;
REEVES, WC .
ANNALS OF INTERNAL MEDICINE, 1994, 121 (12) :953-959
[6]  
GIBBONS RD, 1984, BIOL PSYCHIAT, V19, P935
[7]   The genetic aetiology of somatic distress [J].
Gillespie, NA ;
Zhu, G ;
Heath, AC ;
Hickie, IB ;
Martin, NG .
PSYCHOLOGICAL MEDICINE, 2000, 30 (05) :1051-1061
[8]   HIGH-FREQUENCY OF FIBROMYALGIA IN PATIENTS WITH CHRONIC FATIGUE SEEN IN A PRIMARY CARE PRACTICE [J].
GOLDENBERG, DL ;
SIMMS, RW ;
GEIGER, A ;
KOMAROFF, AL .
ARTHRITIS AND RHEUMATISM, 1990, 33 (03) :381-387
[9]   Unique genetic and environmental determinants of prolonged fatigue: a twin study [J].
Hickie, I ;
Kirk, K ;
Martin, N .
PSYCHOLOGICAL MEDICINE, 1999, 29 (02) :259-268
[10]   Complex genetic and environmental relationships between psychological distress, fatigue and immune functioning: a twin study [J].
Hickie, I ;
Bennett, B ;
Lloyd, A ;
Heath, A ;
Martin, N .
PSYCHOLOGICAL MEDICINE, 1999, 29 (02) :269-277