Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 9 de 9
Filter
Add more filters










Database
Language
Publication year range
2.
Eur Arch Otorhinolaryngol ; 275(5): 1211-1218, 2018 May.
Article in English | MEDLINE | ID: mdl-29520499

ABSTRACT

BACKGROUND: Vocal fold (VF) scarring remains a therapeutic dilemma and challenge in modern laryngology. To facilitate corresponding research, we aimed to establish an in vitro fibrogenesis model employing human VF fibroblasts (hVFF) and the principles of macromolecular crowding (MMC). METHODS: Fibrogenesis was promoted by addition of transforming growth factor-ß1 to standard medium and medium containing inert macromolecules (MMC). Hepatocyte growth factor (HGF) and Botox type A were tested for their antifibrotic properties in various doses. Experiments were analyzed with respect to the biosynthesis of collagen, fibronectin, and α-smooth muscle actin using immunofluorescence, silver stain and western blot. RESULTS: MMC led to favourable enhanced deposition of collagen and other extracellular matrix components, reflecting fibrotic conditions. Low doses of HGF were able to dampen profibrotic effects. This could not be observed for higher HGF concentrations. Botox type A did not show any effects. CONCLUSION: Based on the principles of MMC we could successfully establish a laryngeal fibrogenesis model employing hVFF. Our finding of dose-dependent HGF effects is important before going into clinical trials in humans and has never been shown before. Our model provides a novel option to screen various potential antifibrotic compounds under standardized conditions in a short time.


Subject(s)
Cicatrix/pathology , Fibroblasts/pathology , Vocal Cords/pathology , Biomarkers/metabolism , Blotting, Western , Cells, Cultured , Cicatrix/metabolism , Fibroblasts/metabolism , Fibrosis , Fluorescent Antibody Technique , Hepatocyte Growth Factor/metabolism , Humans , In Vitro Techniques , Vocal Cords/metabolism
3.
Clin Otolaryngol ; 43(4): 1050-1056, 2018 Aug.
Article in English | MEDLINE | ID: mdl-29575651

ABSTRACT

OBJECTIVES: Reliable prognostic markers are lacking for tongue carcinoma. C-reactive protein (CRP) and a ratio from neutrophils/lymphocytes (NLR) are biomarkers, associated with prognosis in solid cancers. Aim of this work was to investigate the role of CRP and NLR in prognosis of patients with tongue carcinoma. DESIGN: Retrospective cohort study. SETTING: We retrospectively analysed data of patients treated for tongue carcinoma at our institution. Levels of CRP, Neutrophils and Lymphocytes were measured pretherapeutic. PARTICIPANTS: 197 patients treated for squamous cell carcinoma of the tongue between 2002 and 2015. MAIN OUTCOME MEASURES: Overall survival, disease-free survival. RESULTS: Elevated CRP was significantly associated with shorter overall survival in our cohort in uni- and multivariate analysis. NLR was not associated with prognosis. CONCLUSION: In the present study we could confirm the role of CRP as an independent prognostic marker in patients with tongue carcinoma. Incorporating this marker in prognostication could represent a valuable and moreover inexpensive tool for improved decisions making concerning therapy in the future.

4.
Clin Otolaryngol ; 41(5): 448-53, 2016 Oct.
Article in English | MEDLINE | ID: mdl-26460806

ABSTRACT

OBJECTIVE: Distribution of age of onset of recurrent respiratory papillomatosis (RRP) is generally described to be bimodal, with peaks at approximately 5 years and 30 years. This assumption has never been scientifically confirmed, and authors tend to refer to an article that does not describe distribution. Knowledge of the distribution of age of onset is important for virological and epidemiological comprehension. The objective of this study was to determine the distribution of age of onset of RRP in a large international sample. DESIGN: Cross-sectional distribution analysis. PARTICIPANTS: Laryngologists from 12 European hospitals provided information on date of birth and date of onset of all their RRP patients treated between 1998 and 2012. Centers that exclusively treated either patients with juvenile onset RRP or patients with adult onset RRP, or were less accessible for one of these groups, were excluded to prevent skewness. MAIN OUTCOME MEASURES: A mixture model was implemented to describe distribution of age of onset. The best fitting model was selected using the Bayesian information criterion. RESULTS: Six hundred and thirty-nine patients were included in the analysis. Age of onset was described by a three component mixture distribution with lognormally distributed components. Recurrent respiratory papillomatosis starts at three median ages 7, 35 and 64 years. CONCLUSIONS: Distribution of age of onset of RRP shows three peaks. In addition to the already adopted idea of age peaks at paediatric and adult age, there is an additional peak around the age of 64.


Subject(s)
Papillomavirus Infections/epidemiology , Respiratory Tract Infections/epidemiology , Adolescent , Adult , Age of Onset , Bayes Theorem , Child , Cross-Sectional Studies , Europe/epidemiology , Female , Humans , Male , Middle Aged
5.
Eur Arch Otorhinolaryngol ; 273(9): 2279-84, 2016 Sep.
Article in English | MEDLINE | ID: mdl-26108198

ABSTRACT

Vocal fold scarring is a relatively small field in scar research with prerequisites found nowhere else. The deterioration of the delicate tri-layered micro-structure of the epithelium of the vocal folds leads to impaired vibration characteristics resulting in a permanent hoarse and breathy voice. Tissue engineering approaches could help to restore the pre-injury status. Despite a considerable progress in this field during the last years, routine clinical applications are not available so far. One reason might be that vocal fold fibroblasts, as the responsible cell type for fibrogenesis, have very particular properties that are only poorly characterized. Moreover, in vivo trials are costly and time consuming and a representative in vitro model does not exist so far. These particular circumstances lead to innovative in vitro strategies and concepts such as macro-molecular crowding that can also be applied in adjacent fields.


Subject(s)
Cicatrix/therapy , Hoarseness/therapy , Postoperative Complications/therapy , Tissue Engineering , Vocal Cords/surgery , Cicatrix/etiology , Fibroblasts , Hoarseness/etiology , Humans , Postoperative Complications/etiology
6.
Andrology ; 1(4): 590-4, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23696116

ABSTRACT

Osteocalcin (OC) - released by osteoblasts and known as a marker of bone turnover - has been suggested to influence male fertility in murine models by enhancing testosterone production and sperm count. Results from clinical studies are scarce, however. The aim of this cross-sectional study was to investigate the proposed association of OC, undercarboxylated osteocalcin (ucOC) or carboxylated osteocalcin (cOC) with testosterone and sperm count in a cohort of 159 young male adults from infertile couples. Semen analysis was performed. Testosterone, free testosterone, LH, OC and ucOC were measured in serum samples after an overnight fast. cOC and OC correlated weakly but significantly with testosterone (OC: r = 0.165, p = 0.040, cOC: r = 0.193, p = 0.017), but not after adjusting for age and body mass index (BMI) or waist-hip ratio (WHR). %ucOC (ucOC levels expressed as percentage of total OC) correlated inversely with LH (r = -0.184, p = 0.023) and remained significant after the same adjustment. No significant correlations were observed between OC, cOC, ucOC, %ucOC and sperm count, semen volume and number of vital spermatozoa. In binary logistic regression analyses, none of the parameters of OC were predictors of oligozoospermia after adjusting for age and BMI or WHR. The weak association between %ucOC and LH has marginal clinical importance because of the lack of associations of parameters of OC with testosterone and sperm count. The current data thus cannot support the notion that OC is associated with male fertility in young men from infertile couples.


Subject(s)
Fertility , Infertility, Male/diagnosis , Oligospermia/diagnosis , Osteocalcin/blood , Sperm Count , Testosterone/blood , Adult , Biomarkers/blood , Cross-Sectional Studies , Humans , Infertility, Male/blood , Infertility, Male/pathology , Infertility, Male/physiopathology , Linear Models , Logistic Models , Luteinizing Hormone/blood , Male , Oligospermia/blood , Oligospermia/pathology , Oligospermia/physiopathology , Predictive Value of Tests , Risk Factors
7.
Eur Arch Otorhinolaryngol ; 270(5): 1679-87, 2013 May.
Article in English | MEDLINE | ID: mdl-23377227

ABSTRACT

Intralesional use of cidofovir (Vistide(®)) has been one of the mainstays of adjuvant therapy in patients with recurrent respiratory papillomatosis (RRP) since 1998. In 2011, a communication provided by the producer of cidofovir addressed very serious side effects concerning its off-label use. As this was a general warning, it was inconclusive whether this would account for its use in RRP. The aim of this study is to determine whether nephrotoxic, neutropenic, or oncogenic side effects have occurred after intralesional use of cidofovir in patients with RRP. Update of recent developments in RRP, a multicentre questionnaire and a multicentre retrospective chart review. Sixteen hospitals from eleven countries worldwide submitted records of 635 RRP patients, of whom 275 were treated with cidofovir. RRP patients received a median of three intralesional injections (interquartile range 2-6). There were no statistical differences in occurrence of neutropenia or renal dysfunction before and after cidofovir. There was no statistical difference in occurrence of upper airway and tracheal malignancies between the cidofovir and the non-cidofovir group. In this retrospective patient chart review, no clinical evidence was found for more long-term nephrotoxicity, neutropenia or laryngeal malignancies after the administration of intralesional cidofovir in RRP patients.


Subject(s)
Antiviral Agents/adverse effects , Cytosine/analogs & derivatives , Head and Neck Neoplasms/chemically induced , Neutropenia/chemically induced , Organophosphonates/adverse effects , Papillomavirus Infections/drug therapy , Renal Insufficiency/chemically induced , Respiratory Tract Infections/drug therapy , Cidofovir , Combined Modality Therapy , Cytosine/adverse effects , Female , Humans , Injections, Intralesional , Male , Off-Label Use , Papillomavirus Infections/surgery , Papillomavirus Infections/virology , Respiratory Tract Infections/surgery , Respiratory Tract Infections/virology , Retrospective Studies , Treatment Outcome
8.
Eur Arch Otorhinolaryngol ; 270(2): 641-6, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23070260

ABSTRACT

Recurrent respiratory papillomatosis (RRP) is a viral induced disease, associated with exophytic epithelial lesions affecting the upper airways. Problem of treatment is the high recurrence of papilloma growth after surgical removal; therefore adjuvant therapy schemes have been established. Cidofovir was one of the agents used off-label in adjuvant therapy in the last years. However, there is ongoing discussion about the effectiveness and possible side effects. Aim of our study was to share our experience in treatment of RRP with cidofovir during the last 11 years. We analyzed all the data of patients treated for RRP at the Department for Phoniatrics of the Medical University of Graz between 1999 and 2011. 25 out of the 34 treated patients are at the moment under complete remission, in six patients partial remission could be achieved and two patients showed poor response to therapy, therefore the treatment with cidofovir was stopped. 21 patients received one cycle of monthly cidofovir, 11 patients received two and one patient three cycles of therapy. Number of procedures reached from one to six during each cycle. Average cumulative dose of one cycle was 79.7 mg (15-277.5 mg), in one patient 435 mg were used. One patient developed temporary, borderline neutropenia without symptoms. Despite the retrospective approach of this study with the limitation of several incomplete records, our results show promising long-term effects of adjuvant use of cidofovir. During this period, we did not observe any relevant side effects.


Subject(s)
Antiviral Agents/therapeutic use , Cytosine/analogs & derivatives , Organophosphonates/therapeutic use , Papillomavirus Infections/drug therapy , Respiratory Tract Infections/drug therapy , Adolescent , Adult , Aged , Aged, 80 and over , Antiviral Agents/adverse effects , Child , Child, Preschool , Cidofovir , Cytosine/adverse effects , Cytosine/therapeutic use , Female , Humans , Infant , Male , Middle Aged , Organophosphonates/adverse effects , Recurrence , Remission Induction , Young Adult
9.
Eur J Obstet Gynecol Reprod Biol ; 157(2): 175-9, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21530059

ABSTRACT

OBJECTIVE: Given its role in converting testosterone to dihydrotestosterone and cortisol to dihydrocortisol, 5α-reductase may be important in the pathophysiology of the polycystic ovary syndrome (PCOS). Increased activity of this enzyme has already been demonstrated in ovaries of affected women, and might be caused by genetic alterations. The aim of this study was to analyze representative genetic variants of both isoforms of 5α-reductase with regard to PCOS parameters in lean and obese women. STUDY DESIGN: We analyzed one single nucleotide polymorphism (SNP) (rs523349) of the isoform 2 (SRD5A2) and one haplotype of the isoform 1 (SRD5A1), consisting of the two SNPs rs39848 and rs3797179, in 249 women with PCOS and 226 healthy women using a 5'-exonuclease-assay. The genotypes were associated with anthropometric, metabolic and hormonal as well as functional tests in these women. RESULTS: In the investigated haplotype of SRD5A1, the TA variant was associated with an increased frequency of PCOS (P=0.022) and an increased Ferriman-Gallwey Score (hirsutism) (P=0.016) in women with normal weight. The G allele at the examined position of the SRD5A2 showed a decreased frequency of PCOS (P=0.03) in women with normal weight. CONCLUSION: One of the keys in the development of the PCOS is hyperandrogenism, which might be caused by an increased 5α-reductase activity, as it is often seen in obesity. This mechanism might therefore be of importance in lean PCOS patients and contribute to the clinical findings.


Subject(s)
3-Oxo-5-alpha-Steroid 4-Dehydrogenase/genetics , Cholestenone 5 alpha-Reductase/genetics , Membrane Proteins/genetics , Polycystic Ovary Syndrome/genetics , Polymorphism, Single Nucleotide/genetics , Thinness/genetics , Adult , Body Weight/genetics , Case-Control Studies , Female , Genotype , Haplotypes/genetics , Humans , Isoenzymes/genetics , Obesity/epidemiology , Obesity/genetics , Polycystic Ovary Syndrome/epidemiology , Prevalence , Thinness/epidemiology
SELECTION OF CITATIONS
SEARCH DETAIL
...