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Vege, Santhi S

Mayo Clinic

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.

Citations 8

Association of Serum Endocannabinoid Levels with Pancreatitis and Pancreatitis-Related Pain
Goodman, Marc T. , Lombardi, Christina , Torrens, Alexa , Saloman, Jami L. , Yang, Yunlong, Fisher, William E., Fogel, Evan L. , Forsmark, Christopher E. , Conwell, Darwin L. , Hart, Phil A. , Park, Walter G. , Topazian, Mark, Vege, Santhi Swaroop , Andersen, Dana K. , Yadav, Dhiraj , Goodman, Marc T , Vege, Santhi S, Saloman, Jami L , Bresee, Catherine J. , Li, Liang , Forsmark, Chris E. , Conwell, Darwin L. , Van Den Eeden, Stephen K , Bellin, Melena D. , Serrano, José , Pandol, Stephen J. , Piomelli, Daniele

Cannabis & Cannabinoid Research | September 18, 2024 | Volume: 10 | Issue: 1 | Pages: 60-70

10.1089/can.2024.0079 Get It

Background and Aims: This investigation examined the association of pancreatitis and pancreatitis-related pain with serum levels of two endocannabinoid molecules such as anandamide (AEA) and 2-arachidonoylglycerol (2-AG) and two paracannabinoid molecules such as oleoylethanolamide (OEA) and palmitoylethanolamide (PEA). Methods: A case–control study was conducted within the Prospective Evaluation of Chronic Pancreatitis for Epidemiological and Translational Studies, including participants with no pancreas disease ( N = 56), chronic abdominal pain of suspected pancreatic origin or indeterminate chronic pancreatitis (CP) ( N = 22), acute pancreatitis ( N = 33), recurrent acute pancreatitis ( N = 57), and definite CP ( N = 63). Results: Circulating AEA concentrations were higher in women than in men ( p = 0.0499), and PEA concentrations were higher in obese participants than those who were underweight/normal or overweight ( p = 0.003). Asymptomatic controls with no pancreatic disease had significantly ( p = 0.03) lower concentrations of AEA compared with all disease groups combined. The highest concentrations of AEA were observed in participants with acute pancreatitis, followed by those with recurrent acute pancreatitis, chronic abdominal pain/indeterminant CP, and definite CP. Participants with pancreatitis reporting abdominal pain in the past year had significantly ( p = 0.04) higher concentrations of AEA compared with asymptomatic controls. Levels of 2-AG were significantly lower ( p = 0.02) among participants reporting abdominal pain in the past week, and pain intensity was inversely associated with concentrations of 2-AG and OEA. Conclusions: Endocannabinoid levels may be associated with stage of pancreatitis, perhaps through activation of the CB1 receptor. Validation of our findings would support the investigation of novel therapeutics, including cannabinoid receptor-1 antagonists, in this patient population.
Circulating immune signatures across clinical stages of chronic pancreatitis: a pilot study
Hagn-Meincke, Rasmus , Hart, Phil A. , Andersen, Dana K. , Vege, Santhi Swaroop , Fogel, Evan L. , Topazian, Mark , Conwell, Darwin L. , Li, Liang , Drewes, Asbjørn Mohr , Forsmark, Chris E. , Fisher, William E., Yadav, Dhiraj , Olesen, Søren Schou , Park, Walter G. , Vege, Santhi S, Serrano, José , Bellin, Melena D. , Van Den Eeden, Stephen K , Pandol, Stephen J.

European Journal of Gastroenterology & Hepatology | December 4, 2023 | Volume: 36 | Issue: 2 | Pages: 177-183

10.1097/meg.0000000000002691 Get It

Objective This pilot study seeks to identify serum immune signatures across clinical stages of patients with chronic pancreatitis (CP). Methods We performed a cross-sectional analysis of prospectively collected serum samples from the PROspective Evaluation of Chronic Pancreatitis for EpidEmiologic and Translation StuDies-study. CP subjects were categorised into three clinical stages based on the presence/absence of metabolic complications: (1) CP with no diabetes and exocrine pancreatic dysfunction (EPD), (2) CP with either diabetes or EPD, and (3) CP with diabetes and EPD. Blinded samples were analysed using an 80-plex Luminex assay of cytokines/chemokines/adhesion molecules. Group and pairwise comparisons were performed to characterise immune signatures across CP subgroups. Results A total of 135 CP subjects (evenly distributed between clinical stages) and 50 controls were studied. Interleukin-6 (IL-6), interleukin-8 (IL-8), and soluble intercellular adhesion molecule 1 (sICAM-1) were significantly elevated in CP subjects compared to controls. The levels of IL-6 and IL-8 increased with advancing disease stages, with the highest levels observed in CP with diabetes and EPD (clinical stage 3). Furthermore, hepatocyte growth factor and macrophage-derived chemokine were significantly increased in clinical stage 3 compared to controls. Conclusion Our study reveals a progressive elevation in pro-inflammatory cytokines and chemokines with advancing clinical stages of CP. These findings indicate potential targets for the development of disease-modifying interventions.
Perception versus reality: A National Cohort Analysis of the surgery‐first approach for resectable pancreatic cancer
Thiels, Cornelius A. , Habermann, Elizabeth B. , Vege, Santhi Swaroop , Smoot, Rory L. , Kendrick, Michael L. , Nagorney, David M. , Truty, Mark J. , Bergquist, John R , Thiels, Cornelius A , Shubert, Christopher R. , Ivanics, Tommy , Vege, Santhi S, Cleary, Sean P. , Smoot, Rory L , Habermann, Elizabeth , Bergquist, John R. , Grotz, Travis E.

Cancer Medicine | July 21, 2021 | Volume: 10 | Issue: 17 | Pages: 5925-5935

10.1002/cam4.4144 Get It

AbstractIntroductionAlthough surgical resection is necessary, it is not sufficient for long‐term survival in pancreatic ductal adenocarcinoma (PDAC). We sought to evaluate survival after up‐front surgery (UFS) in anatomically resectable PDAC in the context of three critical factors: (A) margin status; (B) CA19‐9; and (C) receipt of adjuvant chemotherapy.MethodsThe National Cancer Data Base (2010–2015) was reviewed for clinically resectable (stage 0/I/II) PDAC patients. Surgical margins, pre‐operative CA19‐9, and receipt of adjuvant chemotherapy were evaluated. Patient overall survival was stratified based on these factors and their respective combinations. Outcomes after UFS were compared to equivalently staged patients after neoadjuvant chemotherapy on an intention‐to‐treat (ITT) basis.ResultsTwelve thousand and eighty‐nine patients were included (n = 9197 UFS, n = 2892 ITT neoadjuvant). In the UFS cohort, only 20.4% had all three factors (median OS = 31.2 months). Nearly 1/3rd (32.7%) of UFS patients had none or only one factor with concomitant worst survival (median OS = 14.7 months). Survival after UFS decreased with each failing factor (two factors: 23 months, one factor: 15.5 months, no factors: 7.9 months) and this persisted after adjustment. Overall survival was superior in the ITT‐neoadjuvant cohort (27.9 vs. 22 months) to UFS.ConclusionDespite the perceived benefit of UFS, only 1‐in‐5 UFS patients actually realize maximal survival when known factors highly associated with outcomes are assessed. Patients are proportionally more likely to do worst, rather than best after UFS treatment. Similarly staged patients undergoing ITT‐neoadjuvant therapy achieve survival superior to the majority of UFS patients. Patients and providers should be aware of the false perception of ‘optimal’ survival benefit with UFS in anatomically resectable PDAC.
Utilisation of artificial intelligence for the development of an EUS-convolutional neural network model trained to enhance the diagnosis of autoimmune pancreatitis
Marya, Neil B. , Powers, Patrick, Chari, Suresh T. , Gleeson, Ferga C. , Leggett, Cadman L. , Dayyeh, Barham K. Abu , Iyer, Prasad G. , Majumder, Shounak , Pearson, Randall K., Petersen, Bret T. , Rajan, Elizabeth , Sawas, Tarek , Vege, Santhi Swaroop, Chen, Shigao , Long, Zaiyang , Hough, David M., Mara, Kristin C. , Levy, Michael J. , Abu Dayyeh, Barham K , Iyer, P G , Majumder, Shounak , Sawas, T , Vege, Santhi S, Mara, Kristin, Mara, Kristin C , Leggett, Cadman L , Chari, Suresh T , Marya, Neil B. , Chandrasekhara, Vinay , Storm, Andrew C. , Vege, Santhi Swaroop , Levy, Michael J.

Gut | October 7, 2020 | Volume: 70 | Issue: 7 | Pages: 1335-1344

10.1136/gutjnl-2020-322821 Get It

Objective The diagnosis of autoimmune pancreatitis (AIP) is challenging. Sonographic and cross-sectional imaging findings of AIP closely mimic pancreatic ductal adenocarcinoma (PDAC) and techniques for tissue sampling of AIP are suboptimal. These limitations often result in delayed or failed diagnosis, which negatively impact patient management and outcomes. This study aimed to create an endoscopic ultrasound (EUS)-based convolutional neural network (CNN) model trained to differentiate AIP from PDAC, chronic pancreatitis (CP) and normal pancreas (NP), with sufficient performance to analyse EUS video in real time. Design A database of still image and video data obtained from EUS examinations of cases of AIP, PDAC, CP and NP was used to develop a CNN. Occlusion heatmap analysis was used to identify sonographic features the CNN valued when differentiating AIP from PDAC. Results From 583 patients (146 AIP, 292 PDAC, 72 CP and 73 NP), a total of 1 174 461 unique EUS images were extracted. For video data, the CNN processed 955 EUS frames per second and was: 99% sensitive, 98% specific for distinguishing AIP from NP; 94% sensitive, 71% specific for distinguishing AIP from CP; 90% sensitive, 93% specific for distinguishing AIP from PDAC; and 90% sensitive, 85% specific for distinguishing AIP from all studied conditions (ie, PDAC, CP and NP). Conclusion The developed EUS-CNN model accurately differentiated AIP from PDAC and benign pancreatic conditions, thereby offering the capability of earlier and more accurate diagnosis. Use of this model offers the potential for more timely and appropriate patient care and improved outcome.
Impact of disconnected pancreatic duct syndrome on endoscopic ultrasound-guided drainage of pancreatic fluid collections
Wang, Lillian , Elhanafi, Sherif , Topazian, Mark , Majumder, Shounak , Levy, Michael J. , Petersen, Bret T. , Martin, John A. , Chari, Suresh T. , Vege, Santhi Swaroop , Abu Dayyeh, Barham K, Vege, Santhi S, Majumder, Shounak , Chari, Suresh T , Storm, Andrew C. , Dayyeh, Barham K. Abu , Levy, Michael J. , Chandrasekhara, Vinay

Endoscopy | July 6, 2020 | Volume: 53 | Issue: 06 | Pages: 603-610

10.1055/a-1213-1489 Get It

Abstract Background Endoscopic intervention for pancreatic fluid collections (PFCs) with disconnected pancreatic duct syndrome (DPDS) has been associated with failures and increased need for additional endoscopic and non-endoscopic interventions. The primary aim of this study was to determine the outcomes of endoscopic ultrasound (EUS)-guided transmural drainage of PFCs in patients with DPDS. Methods In patients undergoing EUS-guided drainage of PFCs from January 2013 to January 2018, demographic profiles, procedural indications and details, adverse events, outcomes, and subsequent interventions were retrospectively collected. Overall treatment success was determined by PFC resolution on follow-up imaging or stent removal without recurrence. Results EUS-guided drainage of PFCs was performed in 141 patients. DPDS was present in 57 of them (40 %) and walled-off necrosis was the most frequent type of PFC (55 %). DPDS was not associated with lower clinical success, increased number of repeat interventions, or increased time to PFC resolution. Patients with DPDS were more likely to be treated with permanent transmural plastic double-pigtail stents (odds ratio [OR] 6.4; 95 % confidence interval [CI] 2.5 – 16.5; P < 0.001). However, when stents were removed, DPDS was associated with increased PFC recurrence after stent removal (OR 8.0; 95 %CI 1.2 – 381.8; P = 0.04). Conclusions DPDS frequently occurs in patients with PFCs but does not negatively impact successful resolution. DPDS is associated with increased PFC recurrence after stent removal.
Recurrent Acute Pancreatitis
Guda, Nalini M. , Muddana, Venkata , Lévy, Philippe, Garg, Pramod Kumar , Coté, Gregory A. , Uç, Aliye , Varadarajulu, Shyam , Vege, Santhi Swaroop , Chari, Suresh T. , Forsmark, Chris E. , Yadav, Dhiraj , Reddy, D. Nageshwar , Tenner, Scott, Johnson, Colin, Akisik, Fatih , Saluja, Ashok K. , Lerch, Markus M. , Mallery, J. Shawn, Freeman, Martin L. , Vege, Santhi S, Whitcomb, David C. , Chari, Suresh T

Pancreas | June 12, 2018 | Volume: 47 | Issue: 6 | Pages: 653-666

10.1097/mpa.0000000000001053 Get It

Abstract Recurrent acute pancreatitis (RAP) is a clinically significant problem globally. The etiology remains unclear in approximately 10% to 15% of patients despite a thorough workup. Data on natural history and efficacy of treatments are limited. We aimed to establish criteria for diagnosis, evaluate the causative factors, and arrive at a consensus on the appropriate workup and management of patients with RAP. The organizing committee was formed, and a set of questions was developed based on the current evidence, controversies, and topics that needed further research. After a vetting process, these topics were assigned to a group of experts from around the world with special interest in RAP. Data were presented as part of a workshop on RAP organized as a part of the annual meeting of the America Pancreatic Association. Pretest and Posttest questions were administered, and the responses were tabulated by the current Grades of Recommendation Assessment, Development and Evaluation system. The consensus guidelines were established in the format of a diagnostic algorithm. Several deficiencies were identified with respect to data on etiology, treatment efficacies, and areas that need immediate research.
Fukuoka criteria accurately predict risk for adverse outcomes during follow-up of pancreatic cysts presumed to be intraductal papillary mucinous neoplasms
Mukewar, Saurabh , Pretis, Nicolò de , Aryal-Khanal, Anupama, Ahmed, Nazir , Sah, Raghuwansh P., Larson, Joseph J. , Levy, Michael J. , Takahashi, Naoki , Topazian, Mark , Pearson, Randall K., Vege, Santhi Swaroop , Chari, Suresh T. , de Pretis, Nicolo, Sah, Raghuwansh, Enders, Felicity , Pearson, Randall, Vege, Santhi S, Takahashi, Naoki , Chari, Suresh T

Gut | July 7, 2016 | Volume: 66 | Issue: 10 | Pages: 1811-1817

10.1136/gutjnl-2016-311615 Get It

Objective Fukuoka consensus guidelines classify pancreatic cystic lesions (PCLs) presumed to be intraductal papillary mucinous neoplasms (IPMNs) into Fukuoka positive (FP) (subgroups of high-risk (HR) and worrisome features (WFs)) and Fukuoka negative (FN) (non-HR feature/WF cysts). We retrospectively estimated 5-year risk of pancreatic cancer (PC) in FN, WF and HR cysts of patients with PCL-IPMN. Design From Mayo Clinic databases, we randomly selected 2000 patients reported to have a PCL; we excluded inflammatory or suspected non-IPMN cysts and those without imaging follow-up. We re-reviewed cross-sectional imaging and abstracted clinical and follow-up data on PCL-IPMNs. The study contained 802 patients with FN cysts and 358 with FP cysts. Results Patients with PCL-IPMN had median (IQR) follow-up of 4.2 (1.8–7.1) years. Among FN cysts, 5-year PC risk was low (2–3%) regardless of cyst size (p=0.67). After excluding events in the first 6 months, 5-year PC risk remained low (0–2%) regardless of cyst size (p=0.61). Among FP cysts, HR cysts (n=66) had greater 5-year PC risk than WF cysts (n=292) (49.7% vs 4.1%; p<0.001). In HR cysts, 3-year PC risk was greatest for obstructive jaundice versus enhancing solid component or main pancreatic duct >10 mm (79.8% vs 37.3% vs 39.4%, respectively; p=0.01). Conclusions Fukuoka guidelines accurately stratify PCL-IPMNs for PC risk, with FN cysts having lowest and HR cysts having greatest risk. After 6-month follow-up, WF and FN cysts had a low 5-year PC risk. Surveillance strategies should be tailored appropriately.
Clinical profiles and outcomes in idiopathic duct-centric chronic pancreatitis (type 2 autoimmune pancreatitis): the Mayo Clinic experience
Hart, Phil A. , Levy, Michael J. , Smyrk, Thomas C. , Takahashi, Naoki , Clain, Jonathan E., Gleeson, Ferga C. , Pearson, Randall K., Petersen, Bret T. , Topazian, Mark , Vege, Santhi Swaroop, Zhang, Lizhi , Chari, Suresh T. , Abu Dayyeh, Barham K, Vege, Santhi S, Levy, Michael J. , Dayyeh, Barham K. Abu , Vege, Santhi Swaroop , Takahashi, Naoki , Chari, Suresh T

Gut | June 17, 2015 | Volume: 65 | Issue: 10 | Pages: 1702-1709

10.1136/gutjnl-2015-309275 Get It

Objective Idiopathic duct-centric chronic pancreatitis (IDCP), also known as type 2 autoimmune pancreatitis (AIP), is an uncommon subtype of AIP. International Consensus Diagnostic Criteria for IDCP propose that the diagnosis requires pancreatic histology and/or concurrent IBD. We examined our experience with IDCP (type 2 AIP) to assess the appropriateness of these criteria, and identify unique characteristics in patients presenting with acute pancreatitis. Design We reviewed the Mayo Clinic AIP database through May 2014 to identify subjects with either definitive (n=31) or probable (n=12) IDCP. We compared demographic and clinical factors based on strength of diagnostic confidence (definitive versus probable), presence of IBD, and acute pancreatitis as the presenting manifestation. Relapse-free survival was determined using the Kaplan-Meier method. Results The clinical profiles were similar irrespective of the diagnostic criteria fulfilled. Common clinical presentations included acute pancreatitis (n=25, 58.1%, 12 of whom (27.9%) had recurrent pancreatitis) and pancreatic mass/obstructive jaundice (n=15, 34.9%). The cumulative relapse rate was 10.6% at 3 years (median follow-up 2.9 years). Relapse-free survival was similar for the different diagnostic categories, but was decreased in those initially presenting with acute pancreatitis (p=0.047) or treated with steroids (vs surgery, p=0.049). Conclusions The current diagnostic classification of probable IDCP and the inclusion of IBD as a supportive criterion appear valid, because patients have similar clinical profiles and disease-related outcomes to those with definitive IDCP. Concurrent IBD, especially in young patients, may suggest when IDCP is the underlying cause of recurrent acute pancreatitis, but additional studies are needed for validation.