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1.
Water Res ; 233: 119805, 2023 Apr 15.
Artigo em Inglês | MEDLINE | ID: mdl-36868119

RESUMO

Rapid sand filters (RSF) are an established and widely applied technology for groundwater treatment. Yet, the underlying interwoven biological and physical-chemical reactions controlling the sequential removal of iron, ammonia and manganese remain poorly understood. To resolve the contribution and interactions between the individual reactions, we studied two full-scale drinking water treatment plant configurations, namely (i) one dual-media (anthracite and quartz sand) filter and (ii) two single-media (quartz sand) filters in series. In situ and ex situ activity tests were combined with mineral coating characterization and metagenome-guided metaproteomics along the depth of each filter. Both plants exhibited comparable performances and process compartmentalization, with most of ammonium and manganese removal occurring only after complete iron depletion. The homogeneity of the media coating and genome-based microbial composition within each compartment highlighted the effect of backwashing, namely the complete vertical mixing of the filter media. In stark contrast to this homogeneity, the removal of the contaminants was strongly stratified within each compartment, and decreased along the filter height. This apparent and longstanding conflict was resolved by quantifying the expressed proteome at different filter heights, revealing a consistent stratification of proteins catalysing ammonia oxidation and protein-based relative abundances of nitrifying genera (up to 2 orders of magnitude difference between top and bottom samples). This implies that microorganisms adapt their protein pool to the available nutrient load at a faster rate than the backwash mixing frequency. Ultimately, these results show the unique and complementary potential of metaproteomics to understand metabolic adaptations and interactions in highly dynamic ecosystems.


Assuntos
Compostos de Amônio , Água Subterrânea , Purificação da Água , Manganês/química , Ferro , Compostos de Amônio/química , Amônia , Quartzo , Ecossistema , Água Subterrânea/química , Filtração/métodos , Purificação da Água/métodos
2.
Anticancer Res ; 38(3): 1585-1593, 2018 03.
Artigo em Inglês | MEDLINE | ID: mdl-29491089

RESUMO

BACKGROUND/AIM: In this retrospective study, we compared breast cancer patients treated with and without mistletoe lectin I (ML-I) in addition to standard breast cancer treatment in order to determine a possible effect of this complementary treatment. PATIENTS AND METHODS: This study included 18,528 patients with invasive breast cancer. Data on additional ML-I treatments were reported for 164 patients. We developed a "similar case" method with a distance measure retrieved from the beta variable in Cox regression to compare these patients, after stage adjustment, with their non-ML-1 treated counterparts in order to answer three hypotheses concerning overall survival, recurrence free survival and life quality. RESULTS: Raw data analysis of an additional ML-I treatment yielded a worse outcome (p=0.02) for patients with ML treatment, possibly due to a bias inherent in the ML-I-treated patients. Using the "similar case" method (a case-based reasoning approach) we could not confirm this harm for patients using ML-I. Analysis of life quality data did not demonstrate reliable differences between patients treated with ML-I treatment and those without proven ML-I treatment. CONCLUSION: Based on a "similar case" model we did not observe any differences in the overall survival (OS), recurrence-free survival (RFS), and quality of life data between breast cancer patients with standard treatment and those who in addition to standard treatment received ML-I treatment.


Assuntos
Neoplasias da Mama/tratamento farmacológico , Proteínas Inativadoras de Ribossomos Tipo 2/uso terapêutico , Toxinas Biológicas/uso terapêutico , Idoso , Neoplasias da Mama/patologia , Intervalo Livre de Doença , Humanos , Pessoa de Meia-Idade , Invasividade Neoplásica , Qualidade de Vida , Estudos Retrospectivos , Resultado do Tratamento
3.
Dermatology ; 232(4): 444-52, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27322385

RESUMO

BACKGROUND/AIMS: Topical corticosteroid concerns (TCC) are an important issue in patients with atopic dermatitis, leading to non-adherence with poor disease control and increased health care costs. However, neither the prevalence of TCC in a more comprehensible dermatological population nor the impact of patient information on topical corticosteroids given by clinicians is known. Therefore, we assessed the prevalence, characteristics, and sources of TCC in a dermatological population and the impact of written and oral patient information on TCC. METHODS: A total of 643 outpatients with various skin diseases answered a 12-item questionnaire while waiting for the doctor's visit. Patients with TCC quantified their concerns on a discrete visual analogue scale before and after patient information, which consisted of written and oral information about topical corticosteroids (TCS) given by dermatologists. RESULTS: The prevalence of TCC was 41.5%, and that of TCC-related non-adherence was 28.3%. TCC was positively associated with age <60 years, female gender, use of complementary and alternative medicine (CAM) and non-physician health care profession. The leading concerns were skin atrophy, systemic effects, and impairment of the immune system. The most frequent sources of TCC were negative reports by media, family, or friends. Both written and oral patient information significantly reduced TCC. The number needed to benefit from patient information was approximately 2. Non-responders were more often female, TCS-inexperienced, and users of CAM with an intermediate level of education. CONCLUSIONS: TCC are highly prevalent in dermatological patients. Patient information may lower TCC in almost every second patient.


Assuntos
Dermatite Atópica/tratamento farmacológico , Glucocorticoides/administração & dosagem , Cooperação do Paciente , Pele/patologia , Administração Tópica , Adolescente , Adulto , Idoso , Criança , Pré-Escolar , Estudos Transversais , Dermatite Atópica/diagnóstico , Dermatite Atópica/epidemiologia , Relação Dose-Resposta a Droga , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Prevalência , Inquéritos e Questionários , Suíça/epidemiologia , Fatores de Tempo , Adulto Jovem
4.
Liver Transpl ; 21(6): 792-800, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-25772848

RESUMO

Major hepatectomy or small-for-size liver transplantation may result in postoperative liver failure. So far, no treatment is available to improve liver regeneration. Herein, we studied whether cilostazol, a selective phosphodiesterase III inhibitor, is capable of improving liver regeneration after major hepatectomy. Sprague-Dawley rats (n = 74) were treated with cilostazol (5 mg/kg daily) or a glucose solution and underwent either 70% liver resection or a sham operation. Before and after surgery, hepatic arterial and portal venous blood flow and hepatic microvascular perfusion were analyzed. Liver morphology, function, and regeneration were studied with histology, immunohistochemistry, western blotting, and bile excretion analysis. Cilostazol significantly increased hepatic blood flow and microcirculation before and after hepatectomy in comparison with sham-operated controls. This was associated with an elevation of hepatic vascular endothelial growth factor expression, an increase of hepatocellular proliferation, and an acceleration of liver regeneration. Furthermore, cilostazol protected the tissue of the remnant liver as indicated by an attenuation of hepatocellular disintegration. In conclusion, cilostazol increases hepatic blood perfusion, microcirculation, and liver regeneration after a major hepatectomy. Thus, cilostazol may represent a novel strategy to reduce the rate of liver failure after both extended hepatectomy and small-for-size liver transplantation.


Assuntos
Circulação Hepática/efeitos dos fármacos , Falência Hepática/prevenção & controle , Regeneração Hepática/efeitos dos fármacos , Inibidores da Fosfodiesterase 3/uso terapêutico , Tetrazóis/uso terapêutico , Animais , Apoptose/efeitos dos fármacos , Bile/metabolismo , Cilostazol , Avaliação Pré-Clínica de Medicamentos , Feminino , Fígado/efeitos dos fármacos , Fígado/metabolismo , Modelos Animais , Inibidores da Fosfodiesterase 3/farmacologia , Ratos Sprague-Dawley , Tetrazóis/farmacologia , Fator de Crescimento Transformador beta/metabolismo , Fator A de Crescimento do Endotélio Vascular/metabolismo
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