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Métodos Terapêuticos e Terapias MTCI
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1.
J Trace Elem Med Biol ; 44: 241-246, 2017 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-28965582

RESUMO

Polycystic ovary syndrome (PCOS) is the most common endocrine disorder in women of reproductive age. To date, no systematic study of interactions between selenium status parameters (SSPs: serum selenium concentration, plasma glutathione peroxidase, GPX3, plasma selenoprotein P, SELENOP), sex hormones, thyroid function parameters, and other laboratory parameters in patients with PCOS has been undertaken. Therefore we aimed to compare such parameters in women with PCOS and in the control groups, and to investigate the multidimensional interactions between various parameters in PCOS patients and in controls. The subjects were diagnosed either with PCOS (n=28, 25.4±5.2 y) or with PCOS+Hashimoto disease (n=13, 27.3±5.6 y). Female patients having normal menses were recruited into the first control group (n=70, 26.8±7.3 y) or to the second control group comprising women only with Hashimoto disease (n=10, 26.2±6.9 y). No apparent differences in SSPs between control subjects and patients with PCOS, also complicated with Hashimoto disease, were identified, though such differences were noticeable for total testosterone (tT), sex hormone binding globulin, free androgen index, dehydroepiandrosterone sulfate (DHEAS), and insulin profile. The correlation between tT and DHEAS was found the strongest. The other group of mutually highly and positively correlated parameters consisted of GPX3, follicle stimulating hormone, free triiodothyronine and free thyroxine. All the latter parameters correlated negatively with vitamin D3. SSPs took part in interactions with thyroid hormones, sex hormones and some other parameters, but only for GPX3 such interactions were statistically significant. The significance of these findings remains open for further investigation, particularly in patients with PCOS and/or Hashimoto disease.


Assuntos
Síndrome do Ovário Policístico/sangue , Selênio/sangue , Adulto , Estudos de Casos e Controles , Sulfato de Desidroepiandrosterona/sangue , Feminino , Humanos , Insulina/sangue , Resistência à Insulina , Análise dos Mínimos Quadrados , Globulina de Ligação a Hormônio Sexual/metabolismo , Testosterona/sangue
2.
Przegl Lek ; 56(1): 86-8, 1999.
Artigo em Polonês | MEDLINE | ID: mdl-10375935

RESUMO

For several years there has been the association between the persistent HPV infection (especially with high oncogenic potency i.e. 16, 18) and the cervical intraepithelial neoplasia. The pathomechanism is probably considered with spread of the early virus gene E1, E2 and the suppressor protein p53 complexes. Further on these complexes cause the neoplastic cell transformation. There has also been described the role of impaired immune response in these cases. The abnormalities cover malformation of antigen presenting system APC, decrease of MHC-I and MHC-II heavy chains rate, decrease of the Langer-hans cells and decrease of count and cytotoxic activities of lymphocytes B and NK cells. The invasive and destructive techniques of HPV associated CIN treatment do not respect its pathogenesis. Therefore the new non surgical methods of treatment would play a major role in treatment and prevention of women especially in their reproductive period. The aim of this work was the evaluation of the Iscador QuS and Intron A role in the management of HPV associated CIN. The 60 patients with CIN and HPV have been diagnosed and treated in our clinic for 12 months. Early results present increase of regression and significant decrease of progression rates in both groups of examined women, comparing to the control group. The stationery state rates in this groups of women were similar to the control group.


Assuntos
Antineoplásicos Fitogênicos/uso terapêutico , Antivirais/uso terapêutico , Interferon-alfa/uso terapêutico , Extratos Vegetais/uso terapêutico , Proteínas de Plantas , Displasia do Colo do Útero/tratamento farmacológico , Neoplasias do Colo do Útero/tratamento farmacológico , Feminino , Humanos , Interferon alfa-2 , Infecções por Papillomavirus/complicações , Infecções por Papillomavirus/tratamento farmacológico , Proteínas Recombinantes , Infecções Tumorais por Vírus/complicações , Infecções Tumorais por Vírus/tratamento farmacológico , Neoplasias do Colo do Útero/imunologia , Displasia do Colo do Útero/imunologia
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