07 June 2026 : Clinical Research
[In Press] Computed Tomography and Plasma Proteomics for Early Discrimination of Post-Pancreatitis Diabetes Mellitus
Ran Hu12ACEG, Xiao Zeng3ACE, Gangjing Li1AEG, Jin Ma1AEG, Huiping Yang1AEG, Fang Jiang4B, Zenghui Li5CE, Xiaoming Zhang3AD, Hua Yang1ADDOI: 10.12659/MSM.952904
Med Sci Monit In Press; DOI: 10.12659/MSM.952904
Available online: 2026-06-07, In Press, Corrected Proof
Publication in the "In-Press" formula aims at speeding up the public availability of the pending manuscript while waiting for the final publication. The assigned DOI number is active and citable. The availability of the article in the Medline, PubMed and PMC databases as well as Web of Science will be obtained after the final publication according to the journal schedule
Abstract
BACKGROUND
There is a lack of effective predictive methods for post-pancreatitis diabetes mellitus (PPDM-A) in clinical practice. This exploratory study aimed to identify candidate computed tomography (CT) and plasma proteomic features associated with subsequent PPDM-A and to assess their preliminary discriminatory performance.
MATERIAL AND METHODS
This retrospective single-center study compared CT imaging features and clinical data between post-pancreatitis normal glucose (PPNG-A, n=10) and PPDM-A (n=9) groups. Differential plasma protein expression was analyzed using proteomics. Correlations between CT features and protein features in patients with PPDM-A were also assessed.
RESULTS
The PPDM-A group showed higher incidences of pancreatic necrosis and elevated plasma complement factor I (CFI) levels compared with the PPNG-A group. Plasma coagulation factor XII (F12) and immunoglobulin heavy chain (IgH) levels were significantly decreased in the PPDM-A group. Enzyme-linked immunosorbent assay findings validated CFI; F12 and IgH remain proteomics-derived candidate markers. The combined 3-index model achieved an area under the curve of 0.989 for PPDM-A discrimination in the same discovery cohort. CFI was positively correlated with pancreatic necrosis (P=0.02, R=0.527).
CONCLUSIONS
Plasma CFI, F12, and IgH demonstrated potential predictive value for PPDM-A and may help identify at-risk patients. CFI and F12 were significantly correlated with pancreatic necrosis, suggesting a link between plasma molecular markers and imaging manifestations of PPDM-A. These exploratory findings provide a preliminary experimental basis for early discrimination of PPDM-A. Clinical utility requires confirmation in multicenter studies with larger sample sizes and both internal and external validation.
Keywords: Pancreatitis; Diabetes Mellitus; Proteomics; Computed Tomography
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