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1.
J Adolesc Health ; 58(1): 24-32, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26707227

ABSTRACT

PURPOSE: Health research that includes youth and family stakeholders increases the contextual relevance of findings, which can benefit both the researchers and stakeholders involved. The goal of this study was to identify youth and family adolescent health priorities and to explore strategies to address these concerns. METHODS: Stakeholders identified important adolescent health concerns, perceptions of which were then explored using concept mapping. Concept mapping is a mixed-method participatory research approach that invites input from various stakeholders. In response to prompts, stakeholders suggested ways to address the identified health conditions. Adolescent participants then sorted the statements into groups based on content similarity and rated the statements for importance and feasibility. Multidimensional scaling and cluster analysis were then applied to create the concept maps. RESULTS: Stakeholders identified sexually transmitted infections (STIs) and obesity as the health conditions they considered most important. The concept map for STIs identified 7 clusters: General sex education, support and empowerment, testing and treatment, community involvement and awareness, prevention and protection, parental involvement in sex education, and media. The obesity concept map portrayed 8 clusters: Healthy food choices, obesity education, support systems, clinical and community involvement, community support for exercise, physical activity, nutrition support, and nutrition education. Ratings were generally higher for importance than for feasibility. CONCLUSIONS: The concept maps demonstrate stakeholder-driven ideas about approaches to target STIs and obesity in this context. Strategies at multiple social ecological levels were emphasized. The concept maps can be used to generate discussion regarding these topics and to identify interventions.


Subject(s)
Adolescent Health , Community Participation/methods , Community-Based Participatory Research , Program Development/methods , Adolescent , Cluster Analysis , Ethnicity , Female , Health Education , Humans , Male , Obesity , Patient Care Team , Sexually Transmitted Diseases , Young Adult
2.
Int J Eat Disord ; 47(1): 112-5, 2014 Jan.
Article in English | MEDLINE | ID: mdl-24323528

ABSTRACT

Males comprise a minority of patients with eating disorders (ED). However, men who have sex with men, males with gender identity disorder, and transsexual (TS) males are at increased risk for ED. Little has been published about the unique treatment needs of TS patients with ED. A 19-year-old male-to-female TS patient presented with restrictive eating, purging, and weight loss. History revealed that her ED ideation and behaviors were strongly intertwined with her gender identity. She was admitted and during her hospitalization both her ED and TS status were addressed medically. Physicians treating patients with ED should be aware of patients' gender identities and the ways in which gender identity may impact management and recovery. When appropriate, providers should consider addressing medical treatment toward gender transition concurrently with treatment for ED to facilitate medical stabilization and weight restoration in the manner most consistent with the patient's identified gender.


Subject(s)
Anorexia Nervosa/therapy , Gender Identity , Transgender Persons/psychology , Transsexualism/therapy , Adult , Anorexia Nervosa/complications , Anorexia Nervosa/psychology , Female , Hospitalization , Humans , Male , Risk Factors , Transsexualism/complications , Transsexualism/psychology , Weight Loss
3.
Antimicrob Agents Chemother ; 53(11): 4733-9, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19687234

ABSTRACT

A combination of phenotypic and genotypic methods was used to investigate 70 unique Escherichia coli clinical isolates identified as producing extended-spectrum beta-lactamases (ESBLs) at a medical center in Pittsburgh, PA, between 2007 and 2008. Fifty-seven isolates (81%) produced CTX-M-type ESBLs, among which CTX-M-15 was predominant (n = 46). Isolates producing CTX-M-2, -9, -14, and -65 were also identified. One CTX-M-producing isolate coproduced CMY-2 cephalosporinase. Ten isolates (14%) produced SHV-type ESBLs, either SHV-5 or SHV-7. Two isolates produced only CMY-2 or -32. Pulsed-field gel electrophoresis revealed the presence of two major clusters of CTX-M-15-producing E. coli isolates, one in phylotype B2 (n = 15) and the other in phylotype A (n = 19). Of four phylotype B2 isolates that were able to transfer the bla(CTX-M-15)-carrying plasmids, three showed fingerprints related (>60%) to those of plasmids from phylotype A isolates. In phylotype B2, all CTX-M-15-producing isolates, as well as three isolates producing CTX-M-14, two producing SHV-5, and one producing SHV-7, belonged to the international epidemic clone defined by serotype O25:H4 and sequence type 131. The plasmids from eight of nine CTX-M-15-producing E. coli isolates of phylotype A that were examined were highly related to each other and were also found in two isolates belonging to phylotype D, suggesting horizontal transfer of this bla(CTX-M-15)-carrying plasmid between phylotypes. Our findings underscore the need to further investigate the epidemiology and virulence of CTX-M-producing E. coli in the United States.


Subject(s)
Escherichia coli Infections/microbiology , Escherichia coli/genetics , beta-Lactamases/biosynthesis , Drug Resistance, Bacterial/genetics , Electrophoresis, Gel, Pulsed-Field , Escherichia coli/classification , Escherichia coli/drug effects , Escherichia coli/enzymology , Gene Transfer, Horizontal , Humans , Microbial Sensitivity Tests , Plasmids
5.
Ann Neurol ; 59(4): 700-8, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16532490

ABSTRACT

OBJECTIVE: To understand the mechanisms of skeletal muscle destruction and resistance to enzyme replacement therapy in Pompe disease, a deficiency of lysosomal acid alpha-glucosidase (GAA), in which glycogen accumulates in lysosomes primarily in cardiac and skeletal muscles. METHODS: We have analyzed compartments of the lysosomal degradative pathway in GAA-deficient myoblasts and single type I and type II muscle fibers isolated from wild-type, untreated, and enzyme replacement therapy-treated GAA knock-out mice. RESULTS: Studies in myoblasts from GAA knock-out mice showed a dramatic expansion of vesicles of the endocytic/autophagic pathways, decreased vesicular movement in overcrowded cells, and an acidification defect in a subset of late endosomes/lysosomes. Analysis by confocal microscopy of isolated muscle fibers demonstrated that the consequences of the lysosomal glycogen accumulation are strikingly different in type I and II muscle fibers. Only type II fibers, which are the most resistant to therapy, contain large regions of autophagic buildup that span the entire length of the fibers. INTERPRETATION: The vastly increased autophagic buildup may be responsible for skeletal muscle damage and prevent efficient trafficking of replacement enzyme to lysosomes.


Subject(s)
Autophagy/physiology , Endocytosis/physiology , Lysosomal Storage Diseases/physiopathology , Age Factors , Animals , Blotting, Western/methods , Cells, Cultured , Disease Models, Animal , Fluorescent Antibody Technique/methods , Glucan 1,4-alpha-Glucosidase/deficiency , Green Fluorescent Proteins/metabolism , In Vitro Techniques , Lysosomal Storage Diseases/genetics , Lysosomal Storage Diseases/metabolism , Lysosomal-Associated Membrane Protein 1/metabolism , Mice , Mice, Knockout , Microscopy, Electron, Transmission/methods , Muscle Fibers, Skeletal/metabolism , Muscle Fibers, Skeletal/ultrastructure , Myoblasts/metabolism , Myoblasts/ultrastructure , Time Factors , Transfection/methods , Transport Vesicles/metabolism , Transport Vesicles/ultrastructure , Tubulin/metabolism
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