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1.
J Clin Virol ; 111: 29-32, 2019 02.
Article in English | MEDLINE | ID: mdl-30639844

ABSTRACT

BACKGROUND: For infection control measures, rapid accurate diagnostics on admission of patients with suspected seasonal influenza is crucial. OBJECTIVE: Prospective comparison of three rapid molecular tests for detection of influenza A/B RNA. STUDY DESIGN: Outpatients presenting at the Medical emergency department of Graz University Hospital with influenza-like illness and a requirement for hospitalization (n = 312) were studied. Nasopharyngeal swabs were collected with the 3 mL-version of the UTM™ Viral Transport Medium (Copan). Specimens were tested for influenza A and B RNA using the Alere™ i Influenza A & B (Abbott), the cobas® Influenza A/B (Roche), and the Xpert® Xpress Flu/RSV (Cepheid) tests. Results were compared to those obtained from the same specimen by the Influenza A/B R-GENE® (bioMerieux) test based on real-time PCR as reference method. RESULTS: Overall sensitivities of the Abbott, Roche, and Cepheid tests were 90.5%, 96.0%, and 97.0%, overall specificities 99.4%, 97.6%, and 98.2% respectively. With the Abbott and the Cepheid tests, all specimens gave valid results, while the Roche test showed invalid results in 37 (12.1%) specimens. Total time to result for the Abbott, Roche, and Cepheid tests was 18 min, 22 min, and 32 min respectively. CONCLUSIONS: The Abbott test lacked sensitivity, the Roche test was impaired by a high number of invalid results. Overall, despite the longest total time to result, the Cepheid test showed the best performance to detect influenza virus RNA in symptomatic patients presenting at an emergency unit in this study.


Subject(s)
Influenza, Human/diagnosis , Molecular Diagnostic Techniques/methods , RNA, Viral/isolation & purification , Emergency Service, Hospital , Humans , Influenza A virus/isolation & purification , Influenza B virus/isolation & purification , Influenza, Human/virology , Nasopharynx/virology , Point-of-Care Systems , Prospective Studies , Reagent Kits, Diagnostic , Sensitivity and Specificity
2.
Cutan Ocul Toxicol ; 37(3): 210-217, 2018 Sep.
Article in English | MEDLINE | ID: mdl-29216751

ABSTRACT

CONTEXT: Contact with pollen is the major reason for the development of allergic symptoms on the ocular surface leading to a significant increase of allergic diseases worldwide. Environmental changes such as increased ultraviolet (UV) radiation and air pollution are discussed as contributory causes for this increase. OBJECTIVE: We investigated the effect of UV light on the histamine content of pollen and examined if an irradiation of pollen affects the viability and proliferation of conjunctival cells. MATERIALS AND METHODS: Alder (Alnus glutinosa) and hazel (Corylus avellana) pollen were irradiated for different time periods with sunlight, UV-A or UV-B light and the histamine content was analysed and compared with non-irradiated pollen. Conjunctival epithelial cells (CHANG cells) were exposed to irradiated and non-irradiated pollen followed by an assessment of cell viability with the colorimetric MTS test and the impedance-based measurement of cell proliferation using the xCELLigence real-time analysis system. RESULTS: UV light irradiation increased the histamine level of alder and hazel pollen in a dose-dependent manner. CHANG cells treated with irradiated pollen induced a statistically significant higher decrease of cell viability than treatment with non-irradiated pollen. DISCUSSION AND CONCLUSIONS: Our results indicate that UV light is able to alter pollen thus making them more harmful for conjunctival cells.


Subject(s)
Allergens/immunology , Conjunctivitis, Allergic/immunology , Histamine/immunology , Pollen/immunology , Ultraviolet Rays/adverse effects , Allergens/radiation effects , Alnus/chemistry , Alnus/immunology , Alnus/radiation effects , Cell Line , Cell Proliferation , Cell Survival/immunology , Conjunctiva/cytology , Conjunctiva/immunology , Corylus/chemistry , Corylus/immunology , Corylus/radiation effects , Dose-Response Relationship, Radiation , Epithelial Cells/immunology , Histamine/radiation effects , Humans , Pollen/chemistry , Pollen/radiation effects
3.
Biofactors ; 42(4): 376-87, 2016 Jul 08.
Article in English | MEDLINE | ID: mdl-27093900

ABSTRACT

Using the menstrual cycle as a model, this study focused on longitudinal changes and associations within a physiological network known to play a role in female fertility, including, as biologically active nodes, NF-κB, leptin and adiponectin, ß-carotene, adipose tissue, and progesterone. In 28 women, leptin, adiponectin, ß-carotene, and progesterone concentrations, NF-κB p65 and p50 activation in peripheral blood mononuclear cells (known to possess estrogen, progesterone and leptin receptors), total body fat (TBF) and subcutaneous adipose tissue (SAT) mass were determined at early (T1) and late follicular (T2) and mid (T3) and late (T4) luteal phase. Leptin and adiponectin concentrations were higher, while NF-κB p65 activation was lower at T3 compared with T1. NF-κB p65 activation was inversely related to leptin concentrations at T1, T3, and T4. ß-Carotene was inversely related to leptin (T1,T2,T4) and SAT (T1,T3,T4). NF-κB p50 activation was inversely related to TBF (T4) and SAT (T3,T4), and leptin was positively related to TBF and SAT (T1-T4). Progesterone was inversely related to leptin (T2,T3), adiponectin (T3), TBF (T3,T4), and SAT (T2,T3,T4). By providing evidence of luteal phase-specific reduced NF-κB p65 activation in women under physiological conditions, this study bridges the gap between existing evidence of a Th1-Th2 immune response shift induced by reduced NF-κB p65 activation and a Th1-Th2 shift previously observed at luteal phase. For the first time, inverse regressions suggest inhibitory effects of leptin on NF-κB p65 activation at luteal phase, along with inhibitory effects of leptin as well as adiponectin on progesterone production in corpus luteum. © 2016 The Authors BioFactors published by Wiley Periodicals, Inc. on behalf of International Union of Biochemistry and Molecular Biology. 24(4):376-387, 2016.


Subject(s)
Follicular Phase/blood , Leptin/blood , Leukocytes, Mononuclear/metabolism , Luteal Phase/blood , Transcription Factor RelA/blood , Adipokines/blood , Adiposity , Adult , Cells, Cultured , Female , Humans , Longitudinal Studies , Progesterone/blood , beta Carotene/blood
4.
Int J Mol Sci ; 16(7): 15776-84, 2015 Jul 10.
Article in English | MEDLINE | ID: mdl-26184174

ABSTRACT

Clotting abnormalities are discussed both in the context with thyroid dysfunctions and obesity caused by a high fat diet. This study aimed to investigate the impact of hypo-, or hyperthyroidism on the endogenous thrombin potential (ETP), a master indicator of clotting activation, on Sprague Dawley rats fed a normal or high fat diet. Female Sprague Dawley rats (n = 66) were grouped into normal diet (ND; n = 30) and high-fat diet (HFD; n = 36) groups and subdivided into controls, hypothyroid and hyperthyroid groups, induced through propylthiouracil or triiodothyronine (T3) treatment, respectively. After 12 weeks of treatment ETP, body weight and food intake were analyzed. Successfully induced thyroid dysfunction was shown by T3 levels, both under normal and high fat diet. Thyroid dysfunction was accompanied by changes in calorie intake and body weight. In detail, compared to euthyroid controls, hypothyroid rats showed significantly increased-and hyperthyroid animals significantly decreased-ETP levels. High fat diet potentiated these effects in both directions. In summary, we are the first to show that hypothyroidism and high fat diet potentiate the thrombotic capacity of the clotting system in Sprague Dawley rats. This effect may be relevant for cardiovascular disease where thyroid function is poorly understood as a pathological contributor in the context of clotting activity and obesogenic nutrition.


Subject(s)
Diet, High-Fat , Hypothyroidism/pathology , Thrombophilia/etiology , Animals , Body Weight , Eating , Female , Hyperthyroidism/chemically induced , Hyperthyroidism/complications , Hyperthyroidism/pathology , Hypothyroidism/chemically induced , Hypothyroidism/complications , Propylthiouracil/toxicity , Rats , Rats, Sprague-Dawley , Triiodothyronine/toxicity
5.
Int J Mol Sci ; 16(5): 11689-98, 2015 May 21.
Article in English | MEDLINE | ID: mdl-26006242

ABSTRACT

Metabolic dysfunctions might play a crucial role in the pathophysiology of thyroid dysfunctions. This study aimed to investigate the impact of a controlled diet (normal versus high fat feeding) on hypothyroid and hyperthyroid Sprague Dawley rats. Female Sprague Dawley rats (n = 66) were grouped into normal diet (n = 30) and high-fat diet (n = 36) groups and subdivided into controls, hypothyroid and hyperthyroid groups, induced through propylthiouracil or triiodothyronine (T3) treatment, respectively. After 12 weeks of treatment metabolic parameters, such as oxidized LDL (oxLDL), malondialdehyde (MDA), 4-hydroxynonenal (HNE), the lipid profile, body weight and food intake parameters were analyzed. Successfully induced thyroid dysfunctions were shown by T3 levels, both under normal and high fat diet. Thyroid dysfunctions were accompanied by changes in calorie intake and body weight as well as in the lipid profile. In detail, hypothyroid rats showed significantly decreased oxLDL levels, whereas hyperthyroid rats showed significantly increased oxLDL levels. These effects were seen under high fat diet and were less pronounced with normal feeding. Taken together, we showed for the first time in female SD rats that only hyper-, but not hypothyroidism, is associated with high atherogenic oxidized LDL irrespective of normal or high-fat diet in Sprague Dawley rats.


Subject(s)
Hyperthyroidism/metabolism , Lipoproteins, LDL/metabolism , Thyroid Gland/physiopathology , Aldehydes/blood , Aldehydes/metabolism , Animals , Body Weight , Diet, High-Fat , Female , Hyperthyroidism/blood , Hyperthyroidism/physiopathology , Hypothyroidism/blood , Hypothyroidism/metabolism , Hypothyroidism/physiopathology , Lipid Metabolism , Lipids/blood , Lipoproteins, LDL/blood , Malondialdehyde/blood , Malondialdehyde/metabolism , Rats , Rats, Sprague-Dawley , Thyroid Gland/metabolism
6.
J Voice ; 28(4): 420-3, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24495429

ABSTRACT

INTRODUCTION: Vocal fold (VF) fibroblasts (VFFs) are the central target in developing new strategies for treatment of VF injury and scarring. Nevertheless, only little is known about the basic biological characteristics of these cells. The aim of this study was to explore the impact of age of VFFs on the response to external growth factor stimulation. STUDY DESIGN: In vitro cell study using a rat model. METHODS: VFFs were extracted from young and aged rat VF 3 months after establishing unilateral injury. Resulting scar fibroblasts (SFs) and normal fibroblasts (NFs) were subsequently cultured separately with or without the addition of hepatocyte growth factor (HGF). After 24 and 72 hours, the production of hyaluronic acid (HA) was examined in the supernatant culture media using enzyme-linked immunosorbent assay. RESULTS: Only cultured SF and NF from young animals could be stimulated significantly in the production of HA by HGF. Within these, average percentage increase was higher in NF compared with SF. CONCLUSION: The response of VFFs in cell culture to growth factors stimulation is highly depending on the age of the animals. This is another step in a nearer characterization of scar VFF and could furthermore be an important point when estimating the success of an intervention. Age-depending effects must be considered as an important factor in developing possible therapeutic agents for VF scarring.


Subject(s)
Cicatrix/drug therapy , Dysphonia/drug therapy , Fibroblasts/drug effects , Hepatocyte Growth Factor/pharmacology , Vocal Cords/growth & development , Vocal Cords/injuries , Age Factors , Animals , Cells, Cultured , Cicatrix/pathology , Cicatrix/physiopathology , Disease Models, Animal , Dysphonia/pathology , Dysphonia/physiopathology , Fibroblasts/cytology , Fibroblasts/metabolism , Hyaluronic Acid/metabolism , Male , Rats, Sprague-Dawley , Vocal Cords/drug effects
7.
Eur Arch Otorhinolaryngol ; 271(5): 1107-12, 2014 May.
Article in English | MEDLINE | ID: mdl-24077847

ABSTRACT

Vocal fold (VF) fibroblasts are the central subject of interest in fibrogenesis and wound healing after VF injury. Scar fibroblasts (SF) exhibit an aberrant production of several extracellular matrix (ECM) components which lead either to VF fibrosis or scarless wound healing. This study aimed to investigate the role of age at the time of injury on ECM production of SF. This is designed as an animal study. VF injury was established unilaterally in eight male Sprague-Dawley rats [3 months of age (n = 4), 11 months of age (n = 4)], while the other side was left intact. Three months after injury the larynges were excised and fibroblasts were extracted from VF [normal fibroblasts (NF)­scar fibroblasts (SF)] and cultured in vitro. After first passage, VF fibroblasts were plated in 24-well plates and levels of hyaluronic acid (HA) and collagen type I were determined enzymatically from supernatant after 24 and 72 h. Cultured SF from younger animals produced significantly higher levels of HA compared to NF fibroblasts from the same animals. HA concentrations of the older animals did not differ significantly between the NF and SF cultures, but the range in SF cultures was large. In contrast to previous studies, we found that even 3 months after VF injury cultured SF from young animals expressed higher levels of HA in comparison to SF from older animals. No difference in collagen levels were observed between the younger and older animals. Age of animals is an essential factor during VF healing and has to be considered for study design.


Subject(s)
Cicatrix/pathology , Disease Models, Animal , Extracellular Matrix/pathology , Fibroblasts/pathology , Vocal Cords/pathology , Wound Healing/physiology , Age Factors , Animals , Collagen Type I/analysis , Hyaluronic Acid/analysis , In Vitro Techniques , Male , Rats
8.
Cephalalgia ; 30(11): 1366-74, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20959431

ABSTRACT

OBJECTIVE: Impaired insulin metabolism has been implicated in migraine. However, to date only some putative effects, especially regarding the involvement of adipocytokines and glucagon-like peptides (GLPs), have been described. The aim of the present study was to investigate adipocytokines and GLPs in non-obese female migraineurs. METHODS: Various parameters of the insulin metabolism and body measurements were determined in 84 non-obese female subjects. RESULTS: We found highly significantly increased insulin levels with an odds ratio of 10.62 for migraine. Leptin and GLP-2 levels were also increased and correlated with insulin. Logistic regression analysis of leptin and GLP-2 revealed odds ratios of 3.79 and 4.26 for migraine, respectively, when comparing the lowest with the highest quartile of the test variable in the complete study cohort. DISCUSSION: We show that non-obese female migraineurs suffer from hyperinsulinemia, which is associated with elevated leptin and GLP-2 levels. Increased leptin and GLP-2 are risk factors for migraine. Our data suggest that migraine is associated with a higher risk for insulin resistance and its clinical consequences.


Subject(s)
Glucagon-Like Peptide 2/blood , Hyperinsulinism/complications , Hyperinsulinism/metabolism , Leptin/blood , Migraine Disorders/complications , Migraine Disorders/metabolism , Adult , Body Mass Index , Enzyme-Linked Immunosorbent Assay , Female , Humans , Risk Factors
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