Narahari Samudrala, Vidya S. Farook, Gerald D. Dodd, Sobha Puppala, Jennifer Schneider, Sharon Fowler, Richard Granato, Thomas D. Dyer, Rector Arya, Laura Almasy, Christopher P. Jenkinson, Andrew K. Diehl, John Blangero, Ravindranath Duggirala
Human Biology 80 (1), 11-28, (1 February 2008) https://doi.org/10.3378/1534-6617(2008)80[11:AGLATI]2.0.CO;2
KEYWORDS: gallbladder disease, cholelithiasis, cholecystitis, family study, variance components analysis, Mexican Americans, San Antonio Family Diabetes/Gallbladder Study (SAFDGS)
The significance of gallbladder wall thickness (GBWT) in regard to gallbladder disease (GBD) is not completely understood. Thickening of the gallbladder wall has been observed in patients with acute calculous and acalculous cholecystitis and chronic cholecystitis. However, various pathologic processes, such as gallbladder cancer and nonbiliary disorders such as liver cirrhosis and viral hepatitis, could also cause thickening of the gallbladder wall. To date, there is no report available on the genetic factors influencing GBWT. Therefore we sought to estimate the heritability (h2) of GBWT and to perform a genome-wide search to identify the susceptibility genes for GBWT, using data from the San Antonio Family Diabetes/Gallbladder Study (SAFDGS), a family study of Mexican Americans. GBWT was measured by ultrasound. After adjusting for the significant effects of age, sex, GBD (i.e., asymptomatic gallstones), metabolic syndrome, and duration of type 2 diabetes (T2DM), GBWT was found to be under significant and appreciable additive genetic influences (h2 ± SE = 0.38 ± 0.09, P ≤ 0.0001). The strongest evidence for linkage occurred between markers D11S912 and D11S968 on chromosome 11q24–q25 (LOD = 2.7), where we have already shown suggestive evidence for linkage of GBD (LOD = 2.7) in a subset of our SAFDGS data. Potential evidence for linkage occurred at markers D1S1728 (1p31.1; LOD = 1.4) and D16S748 (16p13.1; LOD = 1.4), respectively. In conclusion, our study provides suggestive evidence for linkage of GBWT on chromosome 11q in Mexican Americans, and future tasks of mapping susceptibility gene(s) for GBD and its related traits, such as GBWT, in this chromosomal region can be fruitful.