Evidence map›Paper›PMID 42953272›Full record

ArticleCureus2026

Trajectories of Glycemia Following Acute Pancreatitis: A Prospective Longitudinal Study.

Uppati V Krishna, Bommi Gowrishankar, Mutyala Trivenu V Chowdary, Vamsi D Yadav, Lrs Girinadh, Ravada Kinneresh

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Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Uppati V KrishnaDepartment of Gastroenterology, Great Eastern Medical School and Hospital, Srikakulam, IND.
Bommi GowrishankarDepartment of General Medicine, Great Eastern Medical School and Hospital, Srikakulam, IND.
Mutyala Trivenu V ChowdaryDepartment of Gastroenterology, Great Eastern Medical School and Hospital, Srikakulam, IND.
Vamsi D YadavDepartment of Gastroenterology, Andhra Medical College, Visakhapatnam, IND.
Lrs GirinadhDepartment of Gastroenterology, Andhra Medical College, Visakhapatnam, IND.
Ravada KinnereshDepartment of Dentistry, Great Eastern Medical School and Hospital, Srikakulam, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAcute pancreatitis (AP) may cause persistent disturbances in glucose metabolism that extend beyond the resolution of acute inflammatory episodes. However, the progression of glycemic abnormalities during the early recovery period remains insufficiently characterized, emphasizing the need for prospective longitudinal evaluation. We aimed to evaluate glycemia trajectories after an episode of AP over a 12-month follow-up by determining the cumulative incidence of new-onset prediabetes and diabetes and assessing longitudinal changes in glycemic parameters.

methodsThis prospective longitudinal observational study included 77 adults diagnosed with AP without preexisting diabetes who were followed up for 12 months. We recorded clinical characteristics, pancreatitis severity scores, laboratory investigations, and fasting blood glucose (FBG), postprandial blood glucose (PPBG), and glycated hemoglobin (HbA1c) levels at baseline, six months, and 12 months. Statistical analyses were performed using repeated-measures analysis of variance for longitudinal comparisons, Bonferroni-adjusted post hoc tests, and McNemar's test for categorical outcomes. Statistical significance was set at p < 0.05.

resultsAmong the 77 participants, 45 (58.4%) were male participants, and 39 (50.6%) had biliary pancreatitis. During follow-up, the incidence of prediabetes increased significantly from 12 (15.6%) at six months to 19 (24.7%) at 12 months (p = 0.023), while that of diabetes increased from three (3.9%) to five (6.5%); however, the difference was not statistically significant (p = 0.480). Overall, glycemic abnormalities increased significantly from 15 (19.5%) to 24 (31.2%) (p = 0.008). Repeated-measures analysis demonstrated a significant increase in FBG levels from 96 ± 9.5 to 106 ± 17.0 mg/dL (p < 0.001), PPBG from 127 ± 16.5 to 150 ± 35.0 mg/dL (p = 0.003), and HbA1c from 5.52% ± 0.11% to 6.06 ± 0.40% (p < 0.001) over the 12-month period. Glycemic trajectory analysis showed that 35 (45.5%) participants remained in the normal-stable group, 35 (45.5%) exhibited a moderately stable pattern, and seven (9.1%) demonstrated a high glycemic trajectory.

conclusionProgressive deterioration in glycemic control occurs during the first year following AP, with nearly one-third of the patients developing prediabetes or diabetes. HbA1c demonstrated the greatest longitudinal increase and may serve as a sensitive marker for identifying patients at risk for post-pancreatitis dysglycemia. These findings support routine metabolic surveillance after AP to facilitate early diagnosis and timely intervention.

Indexed as

acute pancreatitisdiabetes mellitusglycated hemoglobinlongitudinal studyprediabetestype 3c

Identifiers

PMID42953272
PMCPMC13714189

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.