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1.
J Endocrinol Invest ; 42(7): 815-824, 2019 Jul.
Article in English | MEDLINE | ID: mdl-30474798

ABSTRACT

PURPOSE: Periostin is highly expressed in craniopharyngioma (CP)-associated fibroblasts and has been identified as a marker for non-alcoholic fatty liver disease (NAFLD). Half of CP patients with hypothalamic syndrome develop NAFLD. We hypothesized that periostin concentration is elevated in biological fluids of CP and associated with pathological hepatic parameters, indicating increased risk for NAFLD. METHODS: A cross-sectional study on 35 patients with sellar masses (SMP) recruited in the German Childhood Craniopharyngioma Registry (32 CP, 2 xanthogranuloma, 1 pilocytic astrocytoma), three short-statured patients with isolated growth hormone deficiency, five short-statured patients with normal findings in GH-stimulating tests and decreased insulin-like growth factor (IGF)-1 and seven healthy controls. Periostin was measured by Elisa in serum, urine and saliva. RESULTS: Periostin serum, urine and saliva concentrations in CP were similar to concentrations of the other groups. Hypothalamic involvement/hypothalamic lesions, degree of obesity as well as hepatic enzymes were not associated with elevated periostin concentrations. Due to low patient numbers with pathological hepatic parameters, missing imaging data on the degree of steatosis hepatis and the lack of histological proof of NAFLD, no definitive conclusions can be drawn from measured periostin concentrations in serum. Interestingly, the subgroup of patients with decreased IGF-1 levels showed elevated concentrations of serum periostin when compared with other groups. CONCLUSIONS: In CP, periostin concentrations are not associated with known risk factors for NAFLD such as hepatic and metabolic parameters, obesity and hypothalamic lesions. Accordingly, periostin does not seem to be a suitable marker for NAFLD in CP.


Subject(s)
Biomarkers/metabolism , Cell Adhesion Molecules/metabolism , Craniopharyngioma/pathology , Non-alcoholic Fatty Liver Disease/epidemiology , Pituitary Neoplasms/pathology , Adolescent , Adult , Age of Onset , Case-Control Studies , Child , Child, Preschool , Cohort Studies , Craniopharyngioma/metabolism , Cross-Sectional Studies , Female , Humans , Incidence , Infant , Male , Non-alcoholic Fatty Liver Disease/metabolism , Pituitary Neoplasms/metabolism , Prognosis , Young Adult
2.
Infect Control Hosp Epidemiol ; 35(12): 1505-10, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25419773

ABSTRACT

OBJECTIVE: This study aimed to monitor the microbiological effect of cleaning near-patient sites over a 48-hour period with a novel disinfectant, electrolyzed water. SETTING: One ward dedicated to acute care of the elderly population in a district general hospital in Scotland. METHODS: Lockers, left and right cotsides, and overbed tables in 30 bed spaces were screened for aerobic colony count (ACC), methicillin-susceptible Staphylococcus aureus (MSSA), and methicillin-resistant S. aureus (MRSA) before cleaning with electrolyzed water. Sites were rescreened at varying intervals from 1 to 48 hours after cleaning. Microbial growth was quantified as colony-forming units (CFUs) per square centimeter and presence or absence of MSSA and MRSA at each site. The study was repeated 3 times at monthly intervals. RESULTS: There was an early and significant reduction in average ACC (360 sampled sites) from a before-cleaning level of 4.3 to 1.65 CFU/cm(2) at 1 hour after disinfectant cleaning ( P < .0001). Average counts then increased to 3.53 CFU/cm(2) at 24 hours and 3.68 CFU/cm(2) at 48 hours. Total MSSA/MRSA (34 isolates) decreased by 71% at 4 hours after cleaning but then increased to 155% (53 isolates) of precleaning levels at 24 hours. CONCLUSIONS: Cleaning with electrolyzed water reduced ACC and staphylococci on surfaces beside patients. ACC remained below precleaning levels at 48 hours, but MSSA/MRSA counts exceeded original levels at 24 hours after cleaning. Although disinfectant cleaning quickly reduces bioburden, additional investigation is required to clarify the reasons for rebound contamination of pathogens at near-patient sites.


Subject(s)
Cross Infection , Disease Transmission, Infectious/prevention & control , Electrolysis , Equipment Contamination/prevention & control , Methicillin-Resistant Staphylococcus aureus , Water , Colony Count, Microbial , Cross Infection/microbiology , Cross Infection/prevention & control , Disinfectants/chemistry , Disinfectants/pharmacology , Disinfection/methods , Equipment and Supplies, Hospital/microbiology , Humans , Methicillin-Resistant Staphylococcus aureus/drug effects , Methicillin-Resistant Staphylococcus aureus/isolation & purification , Treatment Outcome , Water/chemistry , Water/pharmacology
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