OBJECTIVE: The serotonin system has been implicated in mood and appetite regulation, and the serotonin transporter gene (SLC6A4) is a commonly studied candidate gene for eating pathology. However, most studies have focused on a single polymorphism (5-HTTLPR) in SLC6A4; little research has utilized multiple single nucleotide polymorphisms (SNPs) to investigate associations between SLC6A4 and eating pathology more comprehensively. METHOD: Family-based association tests were conducted for seven polymorphisms in or near SLC6A4, using families from the Colorado Center for Antisocial Drug Dependence. Data were available for 135 families, with phenotypic data available for female twins and female nontwin siblings. Seven items assessed two disordered eating characteristics: weight and shape concerns and behaviors (WSCB) and binge eating (BE). RESULTS: No significant associations were found between any genetic variant and the two disordered eating characteristics. DISCUSSION: This study suggests that utilizing polymorphisms in and near SLC6A4, including 5-HTTLPR, may not be useful in identifying genetic risk factors for disordered eating.
OBJECTIVE: The serotonin system has been implicated in mood and appetite regulation, and the serotonin transporter gene (SLC6A4) is a commonly studied candidate gene for eating pathology. However, most studies have focused on a single polymorphism (5-HTTLPR) in SLC6A4; little research has utilized multiple single nucleotide polymorphisms (SNPs) to investigate associations between SLC6A4 and eating pathology more comprehensively. METHOD: Family-based association tests were conducted for seven polymorphisms in or near SLC6A4, using families from the Colorado Center for Antisocial Drug Dependence. Data were available for 135 families, with phenotypic data available for female twins and female nontwin siblings. Seven items assessed two disordered eating characteristics: weight and shape concerns and behaviors (WSCB) and binge eating (BE). RESULTS: No significant associations were found between any genetic variant and the two disordered eating characteristics. DISCUSSION: This study suggests that utilizing polymorphisms in and near SLC6A4, including 5-HTTLPR, may not be useful in identifying genetic risk factors for disordered eating.
Authors: Kirsty Kiezebrink; Evleen T Mann; Sarah R Bujac; Michael J Stubbins; David A Campbell; John E Blundell Journal: World J Biol Psychiatry Date: 2010-09 Impact factor: 4.132
Authors: K Wang; H Zhang; C S Bloss; V Duvvuri; W Kaye; N J Schork; W Berrettini; H Hakonarson Journal: Mol Psychiatry Date: 2010-11-16 Impact factor: 15.992
Authors: Melissa A Munn; Michael C Stallings; Soo Hyun Rhee; Laura E Sobik; Robin P Corley; Sally Ann Rhea; John K Hewitt Journal: Int J Eat Disord Date: 2010-12 Impact factor: 4.861
Authors: Camden E Matherne; Melissa A Munn-Chernoff; Laura M Thornton; Soo Hyun Rhee; Stacy Lin; Robin P Corley; Michael C Stallings; John K Hewitt Journal: Eat Behav Date: 2019-02-07