Key result
Homozygous T carriers of the SNP rs4846567 near the LYPLAL1 gene had a 7% higher excess BMI loss two years after Roux-en-Y gastric bypass surgery compared to GG/GT carriers (p=0.031).
Why the study?
Does the LYPLAL1 genotype affect excess BMI loss and eating behavior in obese patients following Roux-en-Y gastric bypass surgery?
Cohort (n=251)
Does the LYPLAL1 genotype affect excess BMI loss and eating behavior in obese patients following Roux-en-Y gastric bypass surgery?
Effect estimate: 7% higher
p-value: p=0.031
The LYPLAL1 genotype (rs4846567 TT) is associated with greater excess BMI loss and lower hunger scores two years after Roux-en-Y gastric bypass surgery, suggesting a genetic influence on bariatric surgery outcomes.
Variant near LYPLAL1 linked to modestly greater post-RYGB EBMIL; leaves open replication before any clinical genetic stratification.
OBJECTIVE: Bariatric surgery is the most efficient treatment of severe obesity. We investigated to what extent BMI- or waist-hip ratio (WHR)-related genetic variants are associated with excess BMI loss (EBMIL) two years after Roux-en-Y gastric bypass (RYGB) surgery, and elucidated the affected biological pathways. METHODS: Two-hundred fifty-one obese patients (age: 43 ± 10.7, preoperative BMI: 45.1 ± 6.1 kg/m(2), 186 women) underwent RYGB surgery and were followed up after two years with regard to BMI. Patients were genotyped for 32 single-nucleotide polymorphisms (SNPs) that were investigated with regard to their impact on response to RYGB and preoperatively measured Three Factor Eating Questionnaire (TFEQ) scores. RESULTS: Homozygous T carriers of the SNP rs4846567 in proximity to the Lysophospholipase-like 1 (LYPLAL1) gene showed a 7% higher EBMIL compared to wild-type and heterozygous carriers (p = 0.031). TT-allele carriers showed furthermore lower scores for Hunger (74%, p < 0.001), lower Disinhibition (53%, p < 0.001), and higher Cognitive restraint (21%, p = 0.017) than GG/GT carriers in the TFEQ. Patients within the lowest quartile of Hunger scores had a 32% greater EBMIL compared to patients in the highest quartile (p < 0.001). CONCLUSION: The LYPLAL1 genotype is associated with differences in eating behavior and loss of extensive body weight following RYGB surgery. Genotyping and the use of eating behavior-related questionnaires may help to estimate the RYGB-associated therapy success.
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Bandstein et al. (2016) conducted a cohort in severe obesity (n=251). Homozygous T carriers of SNP rs4846567 (LYPLAL1) vs. Wild-type and heterozygous carriers (GG/GT) was evaluated on excess BMI loss (EBMIL) (7% higher, p=0.031). Homozygous T carriers of the SNP rs4846567 near the LYPLAL1 gene had a 7% higher excess BMI loss two years after Roux-en-Y gastric bypass surgery compared to GG/GT carriers (p=0.031).
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