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1.
Arch. endocrinol. metab. (Online) ; 62(4): 410-415, July-Aug. 2018. tab, graf
Article in English | LILACS | ID: biblio-950086

ABSTRACT

ABSTRACT Objective: The association between coronary artery disease (CAD) and thyroid function remains controversial. We evaluated the thyroid function and graduated well-defined CAD as confirmed by quantitative coronary angiography (CA). Subjects and methods: We evaluated the serum TSH, free thyroxine, free triiodothyronine and thyroid antibody levels in 300 consecutive patients (age 61.6 ± 9.9 years and 54% were male) undergoing CAD diagnosis as confirmed by CA. Plaques with ≥ 50% stenosis being indicative of obstructive CAD, and patients were divided into groups according to main epicardial coronary arteries with plaques (0, 1, 2, 3). Lipid profiles and a homeostasis model assessment (HOMA-IR) were determined. Results: Serum median (25% and 75% percentile) TSH levels in patients with group 2 and 3 (2.25; 1.66-3.12 mU/L and 4.99; 4.38-23.60 mU/L, respectively) had significantly higher TSH concentrations (p < 0.0001) than the group 0 (1.82; 1.35-2.51 mU/L). Furthermore, patients of group 3 had higher TSH concentration (p < 0.0001) than those of group 1 (1.60; 0.89-2.68 mU/L). Group 3 were older (64 ± 8.5 vs. 59 ± 9.5, p = 0.001), had more patients with dyslipidemia (84% versus 58%, p < 0.001), male (54% versus 44%, p = 0.01), hypertension (100% versus 86%, p < 0.001), and smoking (61% versus 33%, p < 0.001) than group 0. Multivariate stepwise logistic analysis showed TSH, age, HbA1c, and HOMA-IR were the CAD associated variables. Conclusions: In this cohort, elevated TSH levels in the high normal range or above are associated with the presence and severity of CAD besides may represent a weak CAD risk factor.


Subject(s)
Humans , Male , Middle Aged , Aged , Coronary Artery Disease/blood , Thyrotropin/blood , Thyroid Function Tests , Thyroxine/blood , Triiodothyronine/blood , Coronary Artery Disease/diagnostic imaging , Glycated Hemoglobin/analysis , Insulin Resistance , Cholesterol/blood , Cross-Sectional Studies , Risk Factors , Age Factors , Coronary Angiography , Coronary Stenosis/diagnostic imaging
3.
Arq. bras. endocrinol. metab ; 56(3): 153-158, Apr. 2012. ilus
Article in English | LILACS | ID: lil-626265

ABSTRACT

Despite recent advances in pharmacological treatment of psychiatric disorders, lithium salts remain frequently used, as they are effective and inexpensive alternatives, especially in the treatment of bipolar disorders. Their use is commonly associated with various endocrine disorders, mainly in thyroid and parathyroid function, and in mineral metabolism. This article aims at reviewing these potential endocrinopathies related to the use of lithium to make health care professionals aware and familiar with these possible complications when they follow up patients using this drug, and to make them able to monitor, identify and institute early and appropriate treatment.


Apesar dos recentes avanços farmacológicos no tratamento dos transtornos psiquiátricos, os sais de lítio permanecem como uma alternativa eficaz e de menor custo, sendo usados com frequência principalmente no tratamento dos transtornos bipolares. O seu uso é comumente relacionado com diversas alterações endocrinológicas, principalmente nas funções tiroidiana, paratiroidiana e do metabolismo iônico. Este artigo tem por objetivo fazer uma revisão dessas potenciais endocrinopatias relacionadas ao uso do lítio, para que, no seguimento de pacientes em uso dessa medicação, os profissionais de saúde estejam atentos e familiarizados com essas possíveis complicações, conseguindo identificar e instituir tratamento precocemente.


Subject(s)
Humans , Endocrine System Diseases/chemically induced , Lithium Compounds/adverse effects , Parathyroid Glands/drug effects , Thyroid Gland/drug effects , Blood Glucose/metabolism , Diabetes Insipidus, Nephrogenic/chemically induced , Mental Disorders/drug therapy
5.
Arq. bras. endocrinol. metab ; 52(5): 854-860, jul. 2008.
Article in Portuguese | LILACS | ID: lil-491853

ABSTRACT

Além de estimular o crescimento estatural, o hormônio de crescimento (GH) promove outros efeitos benéficos nos pacientes com deficiência de GH (DGH). A suspensão do GH em pacientes com DGH, durante o período de transição da criança para a vida adulta, induz a alterações metabólicas desfavoráveis na composição corporal, na integridade óssea, na capacidade para desempenhar atividade física, e também aumenta fatores de risco cardiovasculares. Estes parâmetros melhoram quando a reposição do GH é reiniciada em adultos com DGH. Com base nestas evidências, a reposição do GH não deveria ser suspensa quando o paciente atingisse sua altura final e, sim, mantida durante a vida adulta. Entretanto, considerando que muitos pacientes com diagnóstico de DGH, quando criança, não tem este diagnóstico confirmado no início da vida adulta, é necessário reavaliar a secreção de GH quando o paciente atingir a altura final. A história clínica do paciente, a resposta ao tratamento com GH, a ressonância magnética da região hipotalâmica-hipofisária e a concentração de IGF-1 podem ajudar nesta reavaliação. A realização de testes de estímulo para liberação do GH é necessária, a menos que o paciente apresente lesão estrutural ou genética que justifiquem a deficiência deste hormônio.


Growth hormone (GH) has many beneficial effects in patients with childhood-onset GH deficiency (GHD) in addition to its promotion of linear growth. The discontinuation of GH treatment in GHD patients, during the transition from childhood to adulthood, induces significant unfavorable changes in body composition, skeletal integrity, exercise capacity, and an adverse cardiovascular risk profile. These changes are reversed after the resumption of GH treatment. As the benefits of continuing GH therapy into adulthood has been well established, it is possible that GH replacement therapy will not be stopped once growth has been completed, but it will continue into adult life. Considering that a high proportion of patients with diagnosis of DGH in childhood are no longer GHD in adolescence, the GH status must be retested when growth is completed. Other factors such as clinical history, GH response in childhood, hipotalamic-pituitary MRI and IGF-1 concentration must be considered. Reconfirmation of GHD diagnosis through stimulation testing is usually required, unless there is a proven genetic or structural lesion persistent from childhood.


Subject(s)
Adult , Child , Humans , Dwarfism, Pituitary/drug therapy , Human Growth Hormone/therapeutic use , Cardiovascular Diseases/etiology , Human Growth Hormone/adverse effects , Human Growth Hormone/deficiency , /analysis , Insulin-Like Growth Factor I/analysis , Recombinant Proteins/therapeutic use
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