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Anderson, Michelle A.

https://orcid.org/0000-0002-8416-4218

Mayo Clinic

Mayo Clinic in Arizona

Citations 6

S41 Predictive Yield of Targeted Endoscopic Ultrasound-Guided - Fine Needle Aspiration in Diagnosing Incidental Pancreatic Cysts
Hentz, Joseph G. , Anderson, Michelle A. , Faigel, Douglas O. , Pannala, Rahul , Jue, Terry L., Gurram, Priyatham , Mohammed, Adil Sarvar , Chen, Longwen , Fukami, Norio , Nguyen, Cuong Cao

American Journal of Gastroenterology | October 24, 2024 | Volume: 119 | Issue: 10S | Pages: S31-S32

10.14309/01.ajg.0001028532.15843.fc Get It

S2533 A Rare Metastatic Presentation of Leiomyosarcoma Every Gastroenterologist Should Know
Worden, Astin, Anderson, Michelle A. , Shaikh, Danial

American Journal of Gastroenterology | October 24, 2024 | Volume: 119 | Issue: 10S | Pages: S1786-S1787

10.14309/01.ajg.0001039500.91713.25 Get It

S2534 A Rare Case of Solitary Fibrous Tumor of the Pancreas
Worden, Astin, Anderson, Michelle A. , Pannala, Rahul , Shaikh, Danial , Fong, Zhi Ven

American Journal of Gastroenterology | October 24, 2024 | Volume: 119 | Issue: 10S | Pages: S1787-S1787

10.14309/01.ajg.0001039504.22679.87 Get It

S1967 A Rare Case of IgG4 Related Disease Masquerading as Pancreatic Cancer
Pisipati, Sailaja , Sileno, Sean, Pannala, Rahul , Anderson, Michelle A.

American Journal of Gastroenterology | October 18, 2023 | Volume: 118 | Issue: 10S | Pages: S1450-S1450

10.14309/01.ajg.0000957508.17580.17 Get It

Chronic Pancreatitis
Schwarzenberg, Sarah Jane , Uç, Aliye , Zimmerman, Bridget, Wilschanski, Michael , Wilcox, C. Mel , Werlin, Steven L. , Troendle, David M. , Tang, Gong , Slivka, Adam, Sherman, Stuart , Shah, Uzma , Sandhu, Bimaljit S., Romagnuolo, Joseph , Rhee, Sue, Pohl, John F. , Perito, Emily R. , Ooi, Chee Y. , Nathan, Jaimie D. , Muniraj, Thiruvengadam , Morinville, Véronique D., McFerron, Brian A. , Mascarenhas, Maria R., Maqbool, Asim , Liu, Quin , Lin, Tom K. , Lewis, Michele D. , Husain, Sohail Z. , Heyman, Melvin B. , Guda, Nalini M. , Gonska, Tanja , Giefer, Matthew J. , Gelrud, Andrés , Gariepy, Cheryl E. , Gardner, Timothy B. , Freedman, Steven D., Forsmark, Christopher E., Fishman, Douglas S., Coté, Gregory A. , Conwell, Darwin L. , Barth, Bradley, Banks, Peter A. , Anderson, Michelle A. , Amann, Stephen T. , Alkaade, Samer, Abu‐El‐Haija, Maisam , Abberbock, Judah , Lowe, Mark E. , Yadav, Dhiraj , Lewis, Michele, Lewis, Michele D , Whitcomb, David C. , Singh, Vikesh K. , Himes, Ryan , Brand, Randall E. , Bellin, Melena D.

Journal of Pediatric Gastroenterology and Nutrition | February 2, 2019 | Volume: 68 | Issue: 4 | Pages: 566-573

10.1097/mpg.0000000000002279 Get It

ABSTRACTObjectives:The aim of the present study was to investigate the natural history of chronic pancreatitis (CP); patients in the North American Pancreatitis Study2 (NAPS2, adults) and INternational Study group of Pediatric Pancreatitis: In search for a cuRE (INSPPIRE, pediatric) were compared.Methods:Demographics, risk factors, disease duration, management and outcomes of 224 children and 1063 adults were compared using appropriate statistical tests for categorical and continuous variables.Results:Alcohol was a risk in 53% of adults and 1% of children (P < 0.0001); tobacco in 50% of adults and 7% of children (P < 0.0001). Obstructive factors were more common in children (29% vs 19% in adults, P = 0.001). Genetic risk factors were found more often in children. Exocrine pancreatic insufficiency was similar (children 26% vs adult 33%, P = 0.107). Diabetes was more common in adults than children (36% vs 4% respectively, P < 0.0001). Median emergency room visits, hospitalizations, and missed days of work/school were similar across the cohorts. As a secondary analysis, NAPS2 subjects with childhood onset (NAPS2‐CO) were compared with INSPPIRE subjects. These 2 cohorts were more similar than the total INSPPIRE and NAPS2 cohorts, including for genetic risk factors. The only risk factor significantly more common in the NAPS2‐CO cohort compared with the INSPPIRE cohort was alcohol (9% NAPS2‐CO vs 1% INSPPIRE cohorts, P = 0.011).Conclusions:Despite disparity in age of onset, children and adults with CP exhibit similarity in demographics, CP treatment, and pain. Differences between groups in radiographic findings and diabetes prevalence may be related to differences in risk factors associated with disease and length of time of CP.
Nutrition and Inflammatory Biomarkers in Chronic Pancreatitis Patients
Greer, Julia B., Greer, Phil J. , Sandhu, Bimaljit S., Alkaade, Samer, Wilcox, C. Mel , Anderson, Michelle A. , Sherman, Stuart , Gardner, Timothy B. , Lewis, Michele D. , Guda, Nalini M. , Muniraj, Thiruvengadam , Conwell, Darwin L. , Coté, Gregory A. , Forsmark, Christopher E., Banks, Peter A. , Tang, Gong , Stello, Kim, Gelrud, Andrés , Slivka, Adam, Whitcomb, David C. , Yadav, Dhiraj , Whitcomb, David C , Lewis, Michele D , Brand, Randall E.

Nutrition in Clinical Practice | August 13, 2018 | Volume: 34 | Issue: 3 | Pages: 387-399

10.1002/ncp.10186 Get It

Abstract Background Chronic pancreatitis (CP) patients frequently experience malabsorption and maldigestion, leading to micronutrient and macronutrient deficiencies. Comorbid diabetes and lifestyle habits, such as alcohol consumption, may impact nutrition status. Methods We compared micronutrient antioxidant, bone metabolism, serum protein, and inflammatory marker levels in 301 CP patients and 266 controls with no known pancreatic disease. We analyzed serum prealbumin and retinol binding protein; vitamins A, D, E, and B12; osteocalcin; tumor necrosis factor‐α; and C‐reactive protein (CRP). We also evaluated biomarkers among subsets of patients, examining factors including time since diagnosis, body mass index, alcohol as primary etiology, diabetes mellitus, vitamin supplementation, and pancreatic enzyme replacement. Results After correcting for multiple comparisons, CP patients had significantly lower levels than controls of the following: vitamin A (40.9 vs 45.4 μg/dL) and vitamin E (α‐tocopherol [8.7 vs 10.3 mg/L] and γ‐tocopherol [1.8 vs 2.2 mg/L]), as well as osteocalcin (7.9 vs 10 ng/mL) and serum prealbumin (23 vs 27 mg/dL). Both patients and controls who took vitamin supplements had higher serum levels of vitamins than those not taking supplements. Compared with controls, in controlled analyses, CP patients had significantly lower levels of vitamins A, D, and E (both α‐tocopherol and γ‐tocopherol). CP patients also had significantly lower levels of osteocalcin, serum prealbumin, and retinol binding protein, and higher CRP. Conclusions CP patients demonstrated lower levels of selected nutrition and bone metabolism biomarkers than controls. Diabetes and alcohol did not impact biomarkers. Vitamin supplements and pancreatic enzyme replacement therapy improved nutrition biomarkers in CP patients.