Genetic studies of late diabetic complications - The overlooked importance of diabetes duration before complication onset

被引:48
作者
Rogus, JJ
Warram, JH
Krolewski, AS
机构
[1] Joslin Diabet Ctr, Sect Genet & Epidemiol, Div Res, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
[3] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
关键词
D O I
10.2337/diabetes.51.6.1655
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Genes play a role in many processes underlying late diabetic complications, but efforts to identify genetic variants have produced disappointing and contradictory results. Here, we evaluate Whether the study designs and analytic methods commonly being used are optimal for finding susceptibility genes for diabetic complications. We do so by generating plausible genetic models and assessing the performance of case-control and family-based trio study designs. What emerges as a key determinant of success is duration of diabetes. This perspective focuses on duration of diabetes before complication onset and its influence on the ability to detect major and minor gene effects. It does not delve into the distinct effect of duration after complication onset, which can enrich case subjects with genotypes conferring survival advantage. We use clinically diagnosed nephropathy in type I diabetes to show how ignoring duration can result in considerable power loss in both case-control and family-based trio designs. We further show how, under certain circumstances, disregard for duration information can paradoxically lead to implicating nonrisk alleles as causative. Our results indicate that problems can be minimized by selecting case subjects with short diabetes duration and, to a lesser extent, control subjects with long duration or, perhaps, by adjusting for duration during analysis.
引用
收藏
页码:1655 / 1662
页数:8
相关论文
共 23 条
[1]   APOE polymorphisms and the development of diabetic nephropathy in type 1 diabetes -: Results of case-control and family-based studies [J].
Araki, S ;
Moczulski, DK ;
Hanna, L ;
Scott, LJ ;
Warram, JH ;
Krolewski, AS .
DIABETES, 2000, 49 (12) :2190-2195
[2]  
Diabet Control Complications Trial Res Grp, 1997, DIABETES, V46, P1829
[3]  
EWENS WJ, 1995, AM J HUM GENET, V57, P455
[4]   Segregation analysis of urinary albumin excretion in families with type 2 diabetes [J].
Fogarty, DG ;
Hanna, LS ;
Wantman, M ;
Warram, JH ;
Krolewski, AS ;
Rich, SS .
DIABETES, 2000, 49 (06) :1057-1063
[5]   Effects of novel polymorphisms in the RAGE gene on transcriptional regulation and their association with diabetic retinopathy [J].
Hudson, BI ;
Stickland, MH ;
Futers, TS ;
Grant, PJ .
DIABETES, 2001, 50 (06) :1505-1511
[6]   Segregation analysis of diabetic nephropathy in Pima Indians [J].
Imperatore, G ;
Knowler, WC ;
Pettitt, DJ ;
Kobes, S ;
Bennett, PH ;
Hanson, RL .
DIABETES, 2000, 49 (06) :1049-1056
[7]   Promoter polymorphism T(-107)C of the paraoxonase PON1 gene is a risk factor for coronary heart disease in type 2 diabetic patients [J].
James, RW ;
Leviev, I ;
Ruiz, J ;
Passa, P ;
Froguel, P ;
Garin, MCB .
DIABETES, 2000, 49 (08) :1390-1393
[8]   RISK OF PROLIFERATIVE DIABETIC-RETINOPATHY IN JUVENILE-ONSET TYPE-I DIABETES - A 40-YR FOLLOW-UP-STUDY [J].
KROLEWSKI, AS ;
WARRAM, JH ;
RAND, LI ;
CHRISTLIEB, AR ;
BUSICK, EJ ;
KAHN, CR .
DIABETES CARE, 1986, 9 (05) :443-452
[9]   Genetics of diabetic nephropathy: Evidence for major and minor gene effects [J].
Krolewski, AS .
KIDNEY INTERNATIONAL, 1999, 55 (04) :1582-1596
[10]   THE CHANGING NATURAL-HISTORY OF NEPHROPATHY IN TYPE-I DIABETES [J].
KROLEWSKI, AS ;
WARRAM, JH ;
CHRISTLIEB, AR ;
BUSICK, EJ ;
KAHN, CR .
AMERICAN JOURNAL OF MEDICINE, 1985, 78 (05) :785-794