Key result
Preoperative µ-opioid receptor availability in the amygdala was associated with subject weight at 24 months following bariatric surgery.
Why the study?
Factors driving individual variability in weight loss or weight regain after bariatric surgery remain elusive, and whether preoperative brain receptor perturbations predict outcomes is unknown.
Does preoperative μ-opioid and dopamine D2 receptor availability predict weight loss following bariatric surgery in morbidly obese women?
Cohort (n=19)
No
Does preoperative μ-opioid and dopamine D2 receptor availability predict weight loss following bariatric surgery in morbidly obese women?
Preoperative μ-opioid receptor availability in the amygdala predicts long-term weight loss outcomes following bariatric surgery, suggesting a role for the opioid system in postoperative weight regain.
Answers are grounded in this paper and cite their sources.
May predict post-bariatric weight variability; hypothesis-generating for reward-system interventions.
Background Bariatric surgery is the most effective method for weight loss in morbid obesity. There is significant individual variability in the weight loss outcomes, yet factors leading to postoperative weight loss or weight regain remain elusive. Alterations in the µ-opioid receptor (MOR) and dopamine D 2 receptor (D 2 R) systems are associated with obesity, appetite control, and reward processing. The magnitude of initial brain receptor system perturbation is a plausible predictor of long-term surgical weight loss outcomes. The aim was to test this hypothesis by measuring obese subjects’ MOR and D 2 R availability with positron emission tomography (PET) preoperatively before bariatric surgery and then assessing their weight development association with regional MOR and D 2 R availabilities at 2-year follow-up. Methods We studied 19 morbidly obese women (mean BMI 40, mean age 43) scheduled to undergo bariatric surgery, i.e. Roux-en-Y gastric bypass or sleeve gastrectomy, according to their standard clinical treatment. Preoperative MOR and D 2 R availabilities were measured using PET with [ 11 C]carfentanil and [ 11 C]raclopride, respectively. Subject weight was recorded at 3, 6, 12, and 24 months after surgery. Radiotracer binding potentials ( BP ND ) were extracted and correlated with patient weight at different time points. ROIs were delineated in the striatum and in limbic and paralimbic components of the emotion and reward networks. Results MOR availabilities were not correlated with preoperative weight. MOR availabilities in the amygdala ( r = −0.54), insula ( r = −0.46), ventral striatum ( r = −0.48) and putamen ( r = −0.49) were associated with subject weight at 3 months. Significant association was found in the amygdala at 6 months ( r = −0.53), 12 ( r = −0.49), and 24 months ( r = −0.50). D 2 R availabilities were associated with neither preoperative weight nor weight loss at any follow-up time point. Conclusions To our knowledge, this is the first study to demonstrate that neuroreceptor markers prior to bariatric surgery in patients with morbid obesity are associated with the postoperative weight loss. Preoperative MOR availability in the amygdala was associated with long-term postoperative weight development after surgery suggesting that postoperative weight regain may derive from dysfunction in the opioid system. Postoperative weight loss outcomes after bariatric surgery may be partially predicted based on preoperative receptor availability opening up new potential for treatment possibilities. Clinical Trials Registration SleevePET2, NCT01373892 , http://www.clinicaltrials.gov
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Karlsson et al. (2021) conducted a cohort in Morbid obesity (n=19). Preoperative µ-opioid receptor (MOR) availability was evaluated on Correlation between preoperative MOR availability in the amygdala and subject weight at 24 months (r = -0.50). Preoperative µ-opioid receptor availability in the amygdala was significantly associated with subject weight at 24 months following bariatric surgery (r = -0.50).
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