The impact of screening for Type 2 diabetes in siblings of patients with established diabetes

被引:17
作者
Farmer, AJ [1 ]
Doll, H
Levy, JC
Salkovskis, PM
机构
[1] Univ Oxford, Dept Primary Hlth Care, Inst Hlth Sci, Oxford OX3 7LF, England
[2] Univ Oxford, Hlth Serv Res Unit, Oxford OX3 7LF, England
[3] Oxford Churchill Hosp, Oxford Ctr Diabet Endocrinol & Metab, Oxford, England
[4] Kings Coll London, Dept Psychol, Inst Psychiat, London WC2R 2LS, England
关键词
diabetes; screening; questionaires; psychology;
D O I
10.1046/j.1464-5491.2003.01042.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Targeted screening for Type 2 diabetes has been proposed as a method of identifying people with, or at risk of, the disease in order to implement preventive care. Aim To assess the changes in anxiety, well-being, and cognitions associated with screening for Type 2 diabetes in people at increased risk of diabetes after 1 year; and to identify potential predictors of increased anxiety and lower well being over this period. Design and setting One-year follow up of a cohort of non-diabetic siblings of those with Type 2 diabetes registered with general practitioners in Oxfordshire and Northamptonshire who were identified for participation in a programme to undertake sib-pair genetic analysis. Methods Potential families were selected through identification of people with Type 2 diabetes. Family members aged 35-74 years, who did not have diabetes and who were willing to participate in the study, completed measures before receiving the results of a fasting plasma glucose test, and 1 year later. Measures included the Spielberger State Anxiety Scale-short form (SSAI-SF), the Well-Being Questionnaire 12 item scale (WBQ-12), and measures of cognitions about developing diabetes. The Health Anxiety Inventory (HAI) was completed before receiving the results of the tests to assess its relationship with anxiety at 1 year. Results A cohort of 431 individuals was identified, of whom 328 (76%) returned fully completed WBQ scales both initially and at 1 year. State anxiety measured with the SSAI-SF fell from 34.5 (95% CI 33.4-35.6) to 32.3 (31.2-33.4) at 1 year (P < 0.0001). Mean WBQ-12 scores rose (i.e. improved) from 26.8 (26.0-27.4) to 27.4 (26.7-28.1) (P = 0.008). SSAI-SF and WBQ-12 mean scores over 1 year did not differ between participants receiving a normal or an at-risk test result. However, those receiving an at-risk test result were more likely, at 1 year, to consider themselves at increased likelihood of developing diabetes (P < 0.001) and to report thinking about what it would be like to develop diabetes (P = 0.006). A score in the upper tertile of the initial HAI was associated with an increased level of anxiety at 1 year (adjusted odds ratio 2.0, 95% CI 1.2-3.4, P = 0.006). Conclusions There is no evidence that an 'at-risk' test result leads to sustained anxiety or reduced well being at 1 year compared with those receiving a normal test result. However, further studies are required to clarify levels of anxiety prior to screening to assess the overall impact of the process.
引用
收藏
页码:996 / 1004
页数:9
相关论文
共 30 条
[1]  
*AM DIAB ASS, 1996, DIABETES CARE S1, V19, pS4
[2]  
[Anonymous], 1997, REC MAN DIAB PRIM CA
[3]  
BECK A T, 1976, P356
[4]  
Beeney L.J., 1994, HDB PSYCHOL DIABETES, P159
[5]  
BRADLEY C, 1993, DIABETIC MED, V10, pS50
[6]  
Bradley C., 1994, HDB PSYCHOL DIABETES
[7]   A COMPARISON OF COGNITIVE THERAPY, APPLIED RELAXATION AND IMIPRAMINE IN THE TREATMENT OF PANIC DISORDER [J].
CLARK, DM ;
SALKOVSKIS, PM ;
HACKMANN, A ;
MIDDLETON, H ;
ANASTASIADES, P ;
GELDER, M .
BRITISH JOURNAL OF PSYCHIATRY, 1994, 164 :759-769
[8]   AVAILABILITY OF TYPE-II DIABETIC FAMILIES FOR DETECTION OF DIABETES SUSCEPTIBILITY GENES [J].
COOK, JTE ;
PAGE, RCL ;
ORAHILLY, S ;
LEVY, J ;
HOLMAN, R ;
BARROW, B ;
HATTERSLEY, AT ;
SHAW, JAG ;
WAINSCOAT, JS ;
TURNER, RC .
DIABETES, 1993, 42 (10) :1536-1543
[9]   QUALITY-OF-LIFE FOLLOWING A FALSE POSITIVE MAMMOGRAM [J].
GRAM, IT ;
LUND, E ;
SLENKER, SE .
BRITISH JOURNAL OF CANCER, 1990, 62 (06) :1018-1022
[10]  
GRIFFIN S, 2001, BMJ-BRIT MED J, V322, P986