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1.
Pituitary ; 19(4): 448-57, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27279011

ABSTRACT

INTRODUCTION: Acromegaly is a rare, insidious disease resulting from the overproduction of growth hormone (GH) and insulin-like growth factor 1 (IGF-1), and is associated with a range of comorbidities. The extent of associated complications and mortality risk is related to length of exposure to the excess GH and IGF-1, thus early diagnosis and treatment is imperative. Unfortunately, acromegaly is often diagnosed late, when patients already have a wide range of comorbidities. The presence of comorbid conditions contributes significantly to patient morbidity/mortality and impaired quality of life. METHODS: We conducted a retrospective literature review for information relating to the diagnosis of acromegaly, and its associated comorbidities using PubMed. The main aim of this review is to highlight the issues of comorbidities in acromegaly, and to reinforce the importance of early diagnosis and treatment. FINDINGS AND CONCLUSIONS: Successful management of acromegaly goes beyond treating the disease itself, since many patients are diagnosed late in disease evolution, they present with a range of comorbid conditions, such as cardiovascular disease, diabetes, hypertension, and sleep apnea. It is important that patients are screened carefully at diagnosis (and thereafter), for common associated complications, and that biochemical control does not become the only treatment goal. Mortality and morbidities in acromegaly can be reduced successfully if patients are treated using a multimodal approach with comprehensive comorbidity management.


Subject(s)
Adenoma/diagnosis , Growth Hormone-Secreting Pituitary Adenoma/diagnosis , Adenoma/complications , Adenoma/epidemiology , Adenoma/therapy , Cardiovascular Diseases/epidemiology , Carpal Tunnel Syndrome/epidemiology , Comorbidity , Diabetes Mellitus/epidemiology , Disease Management , Growth Hormone-Secreting Pituitary Adenoma/complications , Growth Hormone-Secreting Pituitary Adenoma/epidemiology , Growth Hormone-Secreting Pituitary Adenoma/therapy , Headache/etiology , Heart Failure/epidemiology , Humans , Hypertension/epidemiology , Hypertrophy, Left Ventricular/epidemiology , Macroglossia/epidemiology , Osteoarthritis/epidemiology , Prognosis , Sleep Apnea Syndromes/epidemiology , Vision Disorders/etiology
2.
Front Horm Res ; 38: 70-76, 2010.
Article in English | MEDLINE | ID: mdl-20616497

ABSTRACT

Pituitary tumors can be morphologically classified as microadenomas (diameter<1 cm) or macroadenomas (>1 cm), which can be enclosed, invasive and/or expansive. Functionally, they are classified as secreting tumors and clinically non-secreting or 'non-functioning' tumors. Several molecular mechanisms have been studied acting in uncontrolled cell proliferation and the acquisition of resistance to apoptosis. A potential mechanism related to apoptosis control has been found following the isolation and characterization of the ASPP proteins family. All these proteins share sequence similarities in their C-termini, which contains their signature sequences of Ankyrin repeats, SH3 domain and proline-rich region. Recent investigations reported that the expression of iASPP mRNA and protein was increased in non-transformed cells induced to undergo apoptosis and inhibition of iASPP expression in these cells by siRNA reduced apoptosis. Thus, modulation of iASPP expression seems to be an integral part of the apoptotic response. The ASPP proteins family binds to proteins that are key players in controlling apoptosis (P53 and NFkappaB p65 subunit). It has been speculated that the iASPP protein product induces apoptosis by blocking NFkappaB or inhibits apoptosis by blocking P53. By either mechanism, the gene could influence the survival of precancerous lesions.


Subject(s)
Intracellular Signaling Peptides and Proteins/physiology , Pituitary Neoplasms/etiology , Repressor Proteins/physiology , Humans , NF-kappa B/physiology , Tumor Suppressor Protein p53/physiology
3.
Pituitary ; 13(3): 199-206, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20107911

ABSTRACT

Dopamine agonists are the treatment of choice for prolactinomas. However, there are still controversies concerning dose, treatment duration and criteria for drug withdrawal in different clinical situations. The aim of this study was to assess diagnostic and therapeutic approaches to prolactinomas among members of the Brazilian Society of Endocrinology and Metabolism (SBEM). SBEM members answered a questionnaire sent by e-mail that included 18 questions related to controversial issues about the management of prolactinomas. Among SBEM members, 721 (approximately 24% of total) answered the questionnaire. Concerning the diagnosis, 38% of the respondents stated that prolactin levels < 100 ng/ml would exclude the presence of a prolactinoma. Most of them favored the screening for macroprolactin in asymptomatic individuals instead of a routine screening (74% vs. 26%). Regarding the treatment, 70% of the respondents chose cabergoline as the drug of choice to treat macroprolactinomas whereas similar proportions advised cabergoline or bromocriptine as the best treatment for microprolactinomas (52% vs. 48%). Only 20% and 34% of respondents favored treatment withdrawal 2-3 years after prolactin normalization in patients with macroprolactinomas and microprolactinomas, respectively. In case of pregnancy, only 58 and 70% of respondents advocated discontinuation of treatment with dopamine agonists in patients with macroprolactinomas and microprolactinomas, respectively. Finally, only 36% would allow breast-feeding without restriction, 44% would restrict it to patients with microprolactinomas and 20% would not recommend it for women with prolactinomas There are several points of disagreement among SBEM members regarding the management of prolactinomas.


Subject(s)
Prolactinoma/drug therapy , Brazil , Bromocriptine/therapeutic use , Cabergoline , Data Collection , Dopamine Agonists/therapeutic use , Ergolines/therapeutic use , Female , Humans , Pregnancy
4.
In. Sociedade de Cardiologia do Estado de Säo Paulo. SOCESP: cardiologia. Rio de Janeiro, Atheneu, 1996. p.426-32, tab.
Monography in Portuguese | LILACS | ID: lil-263996

ABSTRACT

A obesidade é um distúrbio metabólico com grande prevalência e difusäo por todo o planeta, e certamente relacionada a hábitos sedentários e erros alimentares das populaçöes. Embora seja raramente secundária a causas endócrinas, como hipercortisolismo e hipotiroidismo, na maioria das vezes ela é decorrente do excesso de ingestäo calórica em relaçäo aos gastos energéticos. A influência genética na prevalência familiar do distúrbio (antes atribuída apenas à transmissäo de hábitos alimentares) tem sido cada vez mais valorizada, tanto em relaçäo ao padräo da obesidade como à menor eficiência metabólica: indivíduos acumulam quantidades diferentes de tecido adiposo com o mesmo aporte calórico. Além do comprometimento estético, a obesidade está relacionada a maior morbidade e mortalidade por várias causas. Desta forma, este distúrbio metabólico merece atençäo médica, tanto no diagnóstico diferencial como no tratamento adequado. Neste capítulo vamos focalizar aspectos da fisiopatologia e epidemiologia da obesidade relacionados ao comprometimento cardiovascular, e mostrar a nossa visäo sobre o seu tratamento, incluindo aquele dirigido a pacientes com cardiopatias.


Subject(s)
Humans , Cardiovascular Diseases , Obesity/etiology , Obesity/therapy
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