Brain free fatty acid uptake is elevated in morbid obesity, and is irreversible 6 months after bariatric surgery: A positron emission tomography study. Issue 7 (24th February 2020)

• Record Type: Journal Article
• Authors: Rebelos, Eleni; Hirvonen, Jussi; Bucci, Marco; Pekkarinen, Laura; Nyman, Mikko; Hannukainen, Jarna C.; Iozzo, Patricia; Salminen, Paulina; Nummenmaa, Lauri; Ferrannini, Ele; Nuutila, Pirjo
• Is Part Of: Diabetes, obesity & metabolism. Volume 22:Issue 7(2020)
• Page Start: 1074
• Page End: 1082
• Publication Date: 2020-02-24
• Subjects: bariatric surgery -- brain metabolism -- free fatty acids -- obesity -- positron emission tomography; Diabetes -- Periodicals; Obesity -- Periodicals; Metabolism -- Disorders -- Periodicals; Clinical pharmacology -- Periodicals; 616.462
• DOI: 10.1111/dom.13996
• Languages: English
• ISSNs: 1462-8902

Abstract

Abstract: Aim: To investigate whether there are differences in brain fatty acid uptake (BFAU) between morbidly obese and lean subjects, and the effect of weight loss following bariatric surgery. Materials and methods: We measured BFAU with 14( R, S)‐[ 18 F]fluoro‐6‐thia‐heptadecanoic acid and positron emission tomography in 24 morbidly obese and 14 lean women. Obese subjects were restudied 6 months after bariatric surgery. We also assessed whether there was hypothalamic neuroinflammation in the obese subjects using fluid‐attenuated inversion recovery (FLAIR) magnetic resonance imaging. Results: Obese subjects had a higher BFAU than lean subjects (1.12 [0.61] vs. 0.72 [0.50] μmol 100 g −1 min −1, P = 0.0002), driven by higher fatty acid uptake availability. BFAU correlated positively with BMI ( P = 0.006, r = 0.48), whole body fatty acid oxidation ( P = 0.006, r = 0.47) and leptin levels (P = 0.001, r = 0.54). When BFAU, leptin and body mass index (BMI) were included in the same model, the association between BFAU and leptin was the strongest. BFAU did not correlate with FLAIR‐derived estimates of hypothalamic inflammation. Six months after bariatric surgery, obese subjects achieved significant weight loss (−10 units of BMI). BFAU was not significantly changed (1.12 [0.61] vs. 1.09 [0.39] μmol 100 g −1 min −1, ns), probably because of the ongoing catabolic state. Finally, baseline BFAU predicted worse plasma glucose levels at 2 years of follow‐up. Conclusions: BFAU is increased in morbidly obese compared with lean subjects, and is unchanged 6 months after bariatric surgery. Baseline BFAU predicts worse plasma glucose levels at follow‐up, supporting the notion that the brain participates in the control of whole‐body homeostasis.