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1.
Am J Gastroenterol ; 116(11): 2296-2299, 2021 11 01.
Article En | MEDLINE | ID: mdl-34732676

INTRODUCTION: Vulvar involvement is a rare complication of Crohn's disease (CD). The optimal treatment of vulvar CD is unknown. METHODS: We conducted a 25-year retrospective cohort study of vulvar CD from 3 referral centers. Clinical features and outcomes were studied. RESULTS: Fifty patients were identified. The most common vulvar symptoms were pain (74%), edema (60%), ulcerations (46%), nodules (36%), and abscess (34%). Medical management leading to symptomatic improvement varied, and 5 patients ultimately required surgery. DISCUSSION: Vulvar CD manifests with a broad spectrum of symptoms. Aggressive medical management was frequently effective, although surgery was required in 10% of cases.


Crohn Disease/complications , Vulvar Diseases/etiology , Adolescent , Adult , Child , Child, Preschool , Cohort Studies , Female , Humans , Middle Aged , Retrospective Studies , Vulvar Diseases/diagnosis , Vulvar Diseases/therapy , Young Adult
2.
Gastroenterology ; 160(3): 941-945.e8, 2021 02.
Article En | MEDLINE | ID: mdl-33197449

The increasing incidence of primary and recurring Clostridioides difficile infections (CDI), which evade current treatment strategies, reflects the changing biology of C difficile. Here, we describe a putative plasmid-mediated mechanism potentially driving decreased sensitivity of C difficile to vancomycin treatment. We identified a broad host range transferable plasmid in a C difficile strain associated with lack of adequate response to vancomycin treatment. The transfer of this plasmid to a vancomycin-susceptible C difficile isolate decreased its susceptibility to vancomycin in vitro and resulted in more severe disease in a humanized mouse model. Our findings suggest plasmid acquisition in the gastrointestinal tract to be a possible mechanism underlying vancomycin treatment failure in patients with CDI, but further work is needed to characterize the mechanism by which plasmid genes determine vancomycin susceptibility in C difficile.


Anti-Bacterial Agents/pharmacology , Clostridioides difficile/genetics , Clostridium Infections/drug therapy , Plasmids/genetics , Vancomycin/pharmacology , Animals , Anti-Bacterial Agents/therapeutic use , Clostridioides difficile/drug effects , Clostridioides difficile/isolation & purification , Clostridium Infections/microbiology , Disease Models, Animal , Drug Resistance, Bacterial/genetics , Germ-Free Life , Humans , Mice , Microbial Sensitivity Tests , Plasmids/isolation & purification , Vancomycin/therapeutic use , Whole Genome Sequencing
3.
Mayo Clin Proc ; 95(4): 758-769, 2020 04.
Article En | MEDLINE | ID: mdl-32247350

Clostridioides difficile infection (CDI) is the leading cause of health care-associated infections in the United States. The increasing incidence and recurrence rates of CDI together with its associated morbidity and mortality are great concerns. Newer treatment methods, such as narrow-spectrum antibiotics, monoclonal antibodies, and microbial replacement therapies, are being developed and implemented. We searched PubMed to identify published literature from 2010 to 2018 using the following keywords: Clostridium difficile, treatment, and therapy. Cited references were also used to identify relevant literature. This review focuses on the current standard of therapy and emerging therapies for CDI and summarizes the updated guidelines on treatment of CDI.


Clostridioides difficile , Clostridium Infections/therapy , Anti-Bacterial Agents/therapeutic use , Clostridium Infections/drug therapy , Clostridium Infections/microbiology , Fecal Microbiota Transplantation , Humans , Probiotics/therapeutic use , Recurrence
5.
Nat Commun ; 10(1): 2012, 2019 05 01.
Article En | MEDLINE | ID: mdl-31043597

Small intestinal bacterial overgrowth (SIBO) has been implicated in symptoms associated with functional gastrointestinal disorders (FGIDs), though mechanisms remain poorly defined and treatment involves non-specific antibiotics. Here we show that SIBO based on duodenal aspirate culture reflects an overgrowth of anaerobes, does not correspond with patient symptoms, and may be a result of dietary preferences. Small intestinal microbial composition, on the other hand, is significantly altered in symptomatic patients and does not correspond with aspirate culture results. In a pilot interventional study we found that switching from a high fiber diet to a low fiber, high simple sugar diet triggered FGID-related symptoms and decreased small intestinal microbial diversity while increasing small intestinal permeability. Our findings demonstrate that characterizing small intestinal microbiomes in patients with gastrointestinal symptoms may allow a more targeted antibacterial or a diet-based approach to treatment.


Dysbiosis/microbiology , Gastrointestinal Diseases/microbiology , Gastrointestinal Microbiome/physiology , Intestinal Mucosa/metabolism , Intestine, Small/microbiology , Adolescent , Adult , Aged , Aged, 80 and over , Anti-Bacterial Agents , DNA, Bacterial/isolation & purification , Dietary Fiber/administration & dosage , Dietary Sugars/adverse effects , Dysbiosis/diet therapy , Dysbiosis/drug therapy , Dysbiosis/physiopathology , Female , Gastrointestinal Diseases/diet therapy , Gastrointestinal Diseases/drug therapy , Gastrointestinal Diseases/physiopathology , Healthy Volunteers , Humans , Intestinal Mucosa/microbiology , Intestinal Mucosa/physiopathology , Intestine, Small/metabolism , Intestine, Small/physiopathology , Male , Middle Aged , Permeability , Pilot Projects , Young Adult
7.
Int J Dermatol ; 57(3): 313-316, 2018 Mar.
Article En | MEDLINE | ID: mdl-29243817

BACKGROUND: Conflicting data have been published on whether an association exists between atopic dermatitis (AD) and nonmelanoma skin cancer. This study aimed to determine whether individuals with AD had an increased risk of squamous cell carcinoma (SCC) development. METHODS: We conducted a retrospective, case-control study of patients residing in Olmsted County, Minnesota. Cases were selected from patients seen at Mayo Clinic (Rochester, Minnesota) who had an initial SCC diagnosis (either invasive SCC or SCC in situ) from January 1, 1996, through December 23, 2010. Age- and sex-matched controls were selected from patients seen at Mayo Clinic with no history of SCC before the case event date. RESULTS: Three hundred ninety-nine individuals with a documented history of SCC were identified and matched with 780 controls who did not have a history of SCC. After adjusting for race, smoking history, ionizing radiation exposure, corticosteroid and cyclosporine use, and non-SCC skin cancers, the odds ratio for SCC development between patients with history of AD versus patients without history of AD was 1.75 (95% CI, 1.05-2.93). CONCLUSIONS: Our findings support an increased risk of SCC development in the setting of AD.


Carcinoma, Squamous Cell/epidemiology , Dermatitis, Atopic/epidemiology , Skin Neoplasms/epidemiology , Aged , Aged, 80 and over , Case-Control Studies , Female , Humans , Male , Middle Aged , Minnesota/epidemiology , Retrospective Studies , Risk Assessment
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