TY - JOUR
T1 - An Exploratory Investigation of Genetic Linkage with Body Composition and Fatness Phenotypes
T2 - The Québec Family Study
AU - Borecki, Ingrid B.
AU - Rice, Treva
AU - Pérusse, Louis
AU - Bouchard, Claude
AU - Rao, D. C.
PY - 1994/5
Y1 - 1994/5
N2 - In the present investigation, we have attempted to identify regions of the genome in which “obesity genes” potentially reside using robust sib‐pair linkage analysis. Data were collected on 1,628 individuals in 301 nuclear families residing in the environs of Québec City during the period 1978–1981. In addition to traditional blood group antigens and enzyme polymorphisms, several phenotypes in the obesity domain that are associated with increased morbidity were assessed, including measures relating to heaviness (i.e., the body mass index), body composition and nutrient partitioning (i.e., % body fat), and regional fat distribution without and with standardization for total fat mass (i.e., the sum of six skinfold thicknesses, and the ratio of the sums of trunk to extremity skinfold thicknesses). Three consistent patterns of potential linkage relationships with obesity phenotypes were revealed in these data, involving the marker loci adenosine deaminase, the Kell blood group antigen, and esterase D, which identify chromosomal regions 20q13, 7q33, and 13q14, respectively. Other potential linkages also were identified in the short arm of chromosome 1, interesting because of the presence of the db and fa loci on homologous regions of chromosome 1 in mouse and rat models of obesity, respectively. Each of the tentative linkage relationships reported here warrant follow‐up using alternative methods and require replication in independent studies. 1994 North American Association for the Study of Obesity (NAASO)
AB - In the present investigation, we have attempted to identify regions of the genome in which “obesity genes” potentially reside using robust sib‐pair linkage analysis. Data were collected on 1,628 individuals in 301 nuclear families residing in the environs of Québec City during the period 1978–1981. In addition to traditional blood group antigens and enzyme polymorphisms, several phenotypes in the obesity domain that are associated with increased morbidity were assessed, including measures relating to heaviness (i.e., the body mass index), body composition and nutrient partitioning (i.e., % body fat), and regional fat distribution without and with standardization for total fat mass (i.e., the sum of six skinfold thicknesses, and the ratio of the sums of trunk to extremity skinfold thicknesses). Three consistent patterns of potential linkage relationships with obesity phenotypes were revealed in these data, involving the marker loci adenosine deaminase, the Kell blood group antigen, and esterase D, which identify chromosomal regions 20q13, 7q33, and 13q14, respectively. Other potential linkages also were identified in the short arm of chromosome 1, interesting because of the presence of the db and fa loci on homologous regions of chromosome 1 in mouse and rat models of obesity, respectively. Each of the tentative linkage relationships reported here warrant follow‐up using alternative methods and require replication in independent studies. 1994 North American Association for the Study of Obesity (NAASO)
KW - animal models
KW - body fat content
KW - regional fat distribution
KW - sib‐pair linkage
UR - http://www.scopus.com/inward/record.url?scp=0000082145&partnerID=8YFLogxK
U2 - 10.1002/j.1550-8528.1994.tb00050.x
DO - 10.1002/j.1550-8528.1994.tb00050.x
M3 - Article
C2 - 16355479
AN - SCOPUS:0000082145
SN - 1071-7323
VL - 2
SP - 213
EP - 219
JO - Obesity research
JF - Obesity research
IS - 3
ER -