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1.
Nat Commun ; 15(1): 3344, 2024 Apr 18.
Article in English | MEDLINE | ID: mdl-38637492

ABSTRACT

Coordinated cell interactions within the esophagus maintain homeostasis, and disruption can lead to eosinophilic esophagitis (EoE), a chronic inflammatory disease with poorly understood pathogenesis. We profile 421,312 individual cells from the esophageal mucosa of 7 healthy and 15 EoE participants, revealing 60 cell subsets and functional alterations in cell states, compositions, and interactions that highlight previously unclear features of EoE. Active disease displays enrichment of ALOX15+ macrophages, PRDM16+ dendritic cells expressing the EoE risk gene ATP10A, and cycling mast cells, with concomitant reduction of TH17 cells. Ligand-receptor expression uncovers eosinophil recruitment programs, increased fibroblast interactions in disease, and IL-9+IL-4+IL-13+ TH2 and endothelial cells as potential mast cell interactors. Resolution of inflammation-associated signatures includes mast and CD4+ TRM cell contraction and cell type-specific downregulation of eosinophil chemoattractant, growth, and survival factors. These cellular alterations in EoE and remission advance our understanding of eosinophilic inflammation and opportunities for therapeutic intervention.


Subject(s)
Eosinophilic Esophagitis , Humans , Eosinophilic Esophagitis/genetics , Eosinophilic Esophagitis/pathology , Endothelial Cells/metabolism , Interleukin-13 , Inflammation/genetics
5.
Dig Dis Sci ; 67(1): 14-15, 2022 01.
Article in English | MEDLINE | ID: mdl-34623579

ABSTRACT

Over the course of their careers, gastroenterologists not infrequently move from one practice setting to another. Perhaps the most uncommon path is for a gastroenterologist well established in private practice to transition to a high-powered academic setting in late career. Below is a description of the career path that I chose, written in part to provide career and personal guidance to the next generation of gastroenterologists.


Subject(s)
Career Choice , Career Mobility , Faculty, Medical , Gastroenterologists , Private Practice , Academic Medical Centers , Decision Making , Gastroenterologists/education , Gastroenterologists/psychology , Hospitals, Teaching , Humans
9.
ACG Case Rep J ; 8(1): e00520, 2021 Jan.
Article in English | MEDLINE | ID: mdl-33457439

ABSTRACT

Autoimmune enteropathy (AIE) is a rare autoimmune disorder that has been described both in pediatric and adult patients and usually causes intractable watery diarrhea. The management of AIE is not standardized because the disease shows variable response to different immunosuppressive regimens including corticosteroids, azathioprine, cyclophosphamide, 6-mercaptopurine, tacrolimus, cyclosporine-A, infliximab, vedolizumab, and abatacept. We present a patient with adult-onset AIE and intractable high-volume diarrhea resulting in numerous hospitalizations and temporary parenteral nutrition, who is now successfully maintained on ustekinumab. Therefore, ustekinumab should be considered for further evaluation as a therapeutic option in cases of refractory AIE.

10.
Am J Gastroenterol ; 116(2): 427-428, 2021 02 01.
Article in English | MEDLINE | ID: mdl-32956074
11.
BMC Gastroenterol ; 20(1): 221, 2020 Jul 11.
Article in English | MEDLINE | ID: mdl-32652931

ABSTRACT

BACKGROUND: Previous studies of the relationship between dietary factors and risk of diverticulosis have yielded inconsistent results. We therefore sought to investigate the association between consumption of fruit and vegetables and prevalent diverticulosis. METHODS: Our study population included participants in the Gastrointestinal Disease and Endoscopy Registry (GIDER), a colonoscopy-based longitudinal cohort at the Massachusetts General Hospital, who provided comprehensive information on dietary intake and lifestyle factors using validated questionnaires prior to colonoscopy. Information on presence and location of diverticula was obtained from the endoscopist at the end of each procedure. We used Poisson regression modeling to calculate the prevalence ratios (PRs) and 95% confidence intervals (CIs). RESULTS: Among 549 participants with a mean age of 61 years enrolled in GIDER, we confirmed diverticulosis in 245 (44.6%). The prevalence of diverticulosis appeared to decrease with higher consumption of fruit and vegetables (Ptrend = 0.007 for fruit and 0.008 for vegetables, respectively). Compared to participants with less than five servings of vegetables per week, the multivariable-adjusted PRs of diverticulosis were 0.84 (95% CI, 0.60-1.17) with five to seven servings per week and 0.62 (95% CI, 0.44-0.89) with greater than one serving per day. Similarly, compared to participants with less than five servings per week of fruit, the multivariable-adjusted PR of diverticulosis was 0.60 (95% CI, 0.41-0.87) with greater than one serving per day. These associations were not modified by age, BMI, smoking, or red meat intake (All Pinteraction > 0.055). CONCLUSION: In a colonoscopy-based longitudinal cohort study, we show that higher consumption of fruit and vegetables is associated with lower risk of prevalent diverticulosis.


Subject(s)
Diverticulum , Vegetables , Colonoscopy , Cross-Sectional Studies , Diet , Diverticulum/epidemiology , Fruit , Humans , Longitudinal Studies , Middle Aged , Prevalence , Surveys and Questionnaires
12.
Cancer Prev Res (Phila) ; 13(10): 877-888, 2020 10.
Article in English | MEDLINE | ID: mdl-32718943

ABSTRACT

Low-dose aspirin is recommended by the U.S. Preventive Services Task Force for primary prevention of colorectal cancer in certain individuals. However, broader implementation will require improved precision prevention approaches to identify those most likely to benefit. The major urinary metabolite of PGE2, 11α-hydroxy-9,15-dioxo-2,3,4,5-tetranor-prostane-1,20-dioic acid (PGE-M), is a biomarker for colorectal cancer risk, but it is unknown whether PGE-M is modifiable by aspirin in individuals at risk for colorectal cancer. Adults (N = 180) who recently underwent adenoma resection and did not regularly use aspirin or NSAIDs were recruited to a double-blind, placebo-controlled, randomized trial of aspirin at 81 or 325 mg/day for 8-12 weeks. The primary outcome was postintervention change in urinary PGE-M as measured by LC/MS. A total of 169 participants provided paired urine samples for analysis. Baseline PGE-M excretion was 15.9 ± 14.6 (mean ± S.D, ng/mg creatinine). Aspirin significantly reduced PGE-M excretion (-4.7 ± 14.8) compared with no decrease (0.8 ± 11.8) in the placebo group (P = 0.015; mean duration of treatment = 68.9 days). Aspirin significantly reduced PGE-M levels in participants receiving either 81 (-15%; P = 0.018) or 325 mg/day (-28%; P < 0.0001) compared with placebo. In 40% and 50% of the individuals randomized to 81 or 325 mg/day aspirin, respectively, PGE-M reduction reached a threshold expected to prevent recurrence in 10% of individuals. These results support that aspirin significantly reduces elevated levels of PGE-M in those at increased colorectal cancer risk to levels consistent with lower risk for recurrent neoplasia and underscore the potential utility of PGE-M as a precision chemoprevention biomarker. The ASPIRED trial is registered as NCT02394769.


Subject(s)
Adenoma/pathology , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Aspirin/therapeutic use , Colorectal Neoplasms/pathology , Dinoprostone/metabolism , Adenoma/drug therapy , Adenoma/metabolism , Adolescent , Adult , Aged , Aged, 80 and over , Colorectal Neoplasms/drug therapy , Colorectal Neoplasms/metabolism , Double-Blind Method , Female , Humans , Male , Middle Aged , Young Adult
13.
Clin Gastroenterol Hepatol ; 18(4): 984-986, 2020 04.
Article in English | MEDLINE | ID: mdl-31254673

ABSTRACT

The critical role of the gut microbiome in microscopic colitis (MC) is evident by the observation that fecal diversion is associated with resolution of mucosal inflammation while restoration of fecal stream is associated with recurrence of disease.1 Characterization of the composition and function of the gut microbiome in MC therefore could provide insights into disease pathogenesis.


Subject(s)
Colitis, Microscopic , Colitis , Gastrointestinal Microbiome , Colitis, Microscopic/diagnosis , Dysbiosis , Feces , Humans
15.
BMC Gastroenterol ; 19(1): 200, 2019 Nov 27.
Article in English | MEDLINE | ID: mdl-31775655

ABSTRACT

BACKGROUND: Cerebrospinal fluid ascites is a rare complication of ventriculoperitoneal shunting and is the result of infection and subsequent peritonitis in the majority of cases. Sterile cerebrospinal fluid ascites in which no known infectious etiology is identified, is even more unusual. CASE PRESENTATION: A 26-year-old female with Loeys-Dietz syndrome and congenital hydrocephalus treated with a ventriculoperitoneal shunt, was evaluated after developing new-onset ascites of unclear etiology after abdominal surgery for repair of an aortic aneurysm requiring multiple therapeutic paracenteses. Her serum ascites albumin gradient (SAAG) was greater than 1.1, suggestive of a portal hypertensive etiology. Gram stain as well as multiple cultures of her ascites fluid were both negative. Extensive investigation including hepatic venous portal gradient measurement and liver biopsy revealed no evidence of hepatic disease or portal hypertension. She was ultimately found to have sterile cerebrospinal fluid ascites which was treated successfully with a peritoneovenous shunt. CONCLUSION: Sterile cerebrospinal fluid ascites is a rare clinical entity that has only been reported approximately 50 times in the medical literature. In this report, we also highlight it as a rare cause of high SAAG ascites. Moreover, we describe the use of a peritoneovenous shunt as a novel therapeutic option in the management of this condition.


Subject(s)
Ascites/etiology , Ventriculoperitoneal Shunt/adverse effects , Adult , Ascites/diagnosis , Ascites/therapy , Ascitic Fluid/metabolism , Female , Humans , Hydrocephalus/therapy , Loeys-Dietz Syndrome , Peritoneovenous Shunt , Serum Albumin/metabolism
17.
Gastrointest Endosc ; 88(1): 204-205, 2018 07.
Article in English | MEDLINE | ID: mdl-29935621
18.
Am J Gastroenterol ; 113(6): 914-915, 2018 06.
Article in English | MEDLINE | ID: mdl-29720715
19.
N Engl J Med ; 375(12): 1197, 2016 09 22.
Article in English | MEDLINE | ID: mdl-27653582
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