This prospective, single-center pilot study will evaluate metabolic flux dysregulation in adults with obesity and suspected or confirmed metabolic dysfunction-associated steatotic liver disease (MASLD) who are scheduled for protocol-eligible bariatric surgery at Vanderbilt University Medical Center. Participants will undergo research assessments before surgery, during the planned bariatric surgery encounter, and approximately 6 months after surgery. The study uses non-radioactive stable isotope tracer infusions, serial blood sampling, abdominal MRI/MRE, and research tissue specimens collected only during clinically planned bariatric surgery to quantify hepatic and extrahepatic metabolic fluxes. The primary objective is to determine how hepatic citric acid cycle flux and related metabolic pathways change after bariatric surgery and how these metabolic measures relate to liver fat, liver stiffness, and biopsy-graded MASLD/MASH severity.
MASLD and its progressive form MASH are associated with obesity, insulin resistance, altered hepatic substrate delivery, and changes in mitochondrial metabolism. However, the direction and significance of hepatic citric acid cycle flux changes in human MASLD remain unresolved. This study will apply in vivo metabolic flux analysis using non-radioactive stable isotope tracers to quantify hepatic and extrahepatic metabolic pathway activity in bariatric surgery participants before and after surgery. Participants will complete three study timepoints. Approximately one week before surgery, participants will undergo fasting physical measurements, questionnaires, research blood collection, and abdominal MRI/MRE to quantify liver fat and stiffness. On the day of surgery, participants will receive intravenous infusions of \[¹³C₃\]lactate, \[6,6-²H₂\]-D-glucose, and \[9,9-²H₂\]palmitate for approximately 120 minutes with serial blood collection. During the clinically planned bariatric surgery, research tissue specimens may be collected from liver, omentum, subcutaneous adipose tissue, and skeletal muscle only if the surgeon determines collection can be performed safely without interfering with clinical care. Approximately 6 months after surgery, participants will repeat fasting physical measurements, questionnaires, MRI/MRE, stable isotope tracer infusion, and blood collection; no follow-up tissue biopsies will be collected. Isotope enrichment patterns in plasma metabolites and tissue metabolites will be analyzed by mass spectrometry and modeled using metabolic flux analysis software to estimate hepatic citric acid cycle flux, gluconeogenesis, glucose turnover, free fatty acid turnover, lactate turnover, and selected extrahepatic metabolic fluxes. Liver fat and stiffness will be assessed by MRI/MRE, and intraoperative liver tissue will be scored for MASLD/MASH features using established histologic criteria.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
20
Clinically indicated bariatric surgery, such as Roux-en-Y gastric bypass or sleeve gastrectomy, performed as part of standard clinical care.
Intravenous non-radioactive stable isotope tracers administered for research measurement of metabolic flux: \[¹³C₃\]lactate, \[6,6-²H₂\]-D-glucose, and \[9,9-²H₂\]palmitate.
Abdominal MRI proton density fat fraction and magnetic resonance elastography to assess hepatic fat and stiffness before surgery and approximately 6 months after surgery.
Liver, omentum, subcutaneous adipose tissue, and skeletal muscle specimens collected only during clinically planned bariatric surgery and only if safe in the surgeon's judgment.
Change in hepatic citric acid cycle flux after bariatric surgery
Change in hepatic citric acid cycle flux estimated from stable isotope enrichment patterns, including \[¹³C₃\]lactate-based measurements, before bariatric surgery and approximately 6 months after surgery.
Time frame: Baseline/day of surgery to approximately 6 months post-surgery
Change in hepatic gluconeogenic flux
Estimated from plasma glucose isotope enrichment and metabolic flux modeling
Time frame: Baseline/day of surgery to ~6 months
Change in endogenous glucose production
Estimated using \[6,6-²H₂\]-D-glucose tracer dilution
Time frame: Baseline/day of surgery to ~6 months
Change in free fatty acid turnover
Estimated using \[9,9-²H₂\]palmitate tracer dilution
Time frame: Baseline/day of surgery to ~6 months
Change in lactate turnover / lactate-related flux
Estimated using stable isotope enrichment patterns
Time frame: Baseline/day of surgery to ~6 months
Liver fat by MRI-PDFF
Hepatic fat fraction quantified by MRI-PDFF
Time frame: Baseline to ~6 months
Liver stiffness by MRE
Liver stiffness quantified by magnetic resonance elastography
Time frame: Baseline to ~6 months
Histologic MASLD/MASH severity
Liver biopsy scored for steatosis, inflammation, ballooning, fibrosis, and MASLD activity score
Time frame: Intraoperative baseline only
Extrahepatic metabolic fluxes
Metabolic fluxes in skeletal muscle, omentum, and subcutaneous adipose tissue estimated from intraoperative tissue specimens
Time frame: Intraoperative baseline only
Serum inflammatory markers
Research measurement of inflammatory markers including CRP, cytokines, adhesion molecules, and related biomarkers
Time frame: Baseline/day of surgery; possibly ~6 months if collected
Metabolic hormone profile
Insulin, leptin, C-peptide, GLP-1, GIP, PYY, ghrelin
Time frame: Baseline/day of surgery; possibly ~6 months if collected
Bile acid profile
Bile acids measured by LC-IM-MS
Time frame: Baseline/day of surgery; possibly ~6 months if collected
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