Computational modeling enables individual assessment of postprandial glucose and insulin responses after bariatric surgery

Onur Poyraz*, Sini Heinonen*, S. T. John, Tuure Saarinen, Anne Juuti, Pekka Marttinen, Kirsi H. Pietiläinen

*Corresponding author for this work

Research output: Contribution to journalArticleScientificpeer-review

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Abstract

Background: Bariatric surgery enhances glucose metabolism, yet the detailed postprandial joint glucose and insulin responses, variability in individual outcomes, and differences in surgical approaches remain poorly understood. Methods: We used hierarchical multi-output Gaussian process (HMOGP) regression to reveal clinically relevant patterns between persons undergoing two types of bariatric surgery by modeling the individual postprandial glucose and insulin responses and estimating the average response curves from individual data. 44 participants with obesity underwent either Roux-en-Y gastric bypass (RYGB; n = 24) or One-Anastomosis gastric bypass (OAGB; n = 20) surgery. The participants were followed up at the 6th and 12th months after the operation, during which they underwent an oral glucose tolerance test (OGTT) and a mixed meal test (MMT). Results: A marked reduction in glycemia, an earlier glucose peak, and an increase and sharpening in the postprandial glucose and insulin responses are evident in both metabolic tests post-operation. MMT results in higher postprandial glucose and insulin peaks compared with OGTT. Higher glucose and insulin responses are observed after RYGB compared with OAGB, suggesting differences between the procedures that may influence the clinical practice. Conclusions: Computational modeling with HMOGP regression can thus be used to, in detail, predict the combined responses of patient cohorts to ingested glucose or a mixed meal and help in assessing individual metabolic improvement after weight loss. This can lead to new knowledge in personalized metabolic interventions.

Original languageEnglish
Article number434
Pages (from-to)1-11
Number of pages11
JournalCommunications Medicine
Volume5
Issue number1
DOIs
Publication statusPublished - Dec 2025
MoE publication typeA1 Journal article-refereed

Funding

The study was supported by the Research Council of Finland (272376, 266286, 314383, and 335443 to K.H.P., 314457 to A.J., 361956 and 338417 to S.H.), the Finnish Medical Foundation (K.H.P., S.H., and A.J.), the Finnish Diabetes Research Foundation (S.H. and K.H.P.), the Orion Foundation (S.H.), the Novo Nordisk Foundation (NNF10OC1013354, NNF17OC0027232, and NNF20OC0060547 to K.H.P. NNF23SA0083953 for S.H.), European Foundation for the Diabetes Research (S.H.), the Paulo Foundation (S.H.), the Gyllenberg Foundation (K.H.P.), Paavo Nurmi Foundation (S.H.), the Sigrid Juselius Foundation (K.H.P.), Helsinki University Hospital Research Funds (S.H., K.H.P., A.J.), Government Research Funds (K.H.P., S.H.), the Research Council of Finland (Flagship program: Finnish Center for Artificial Intelligence FCAI, and grants 352986, 358246 to P.M.) and EU (H2020 grant 101016775 and NextGenerationEU to P.M.).

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