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- Ensaio Clínico NCT01688349
Pattern of Gene Expression in Adipose Tissue From Patients With Cushing Syndrome (LIPOCUSH)
Comparative Study of Subcutaneous and Visceral Adipose Tissue in Patients Affected by Cushing Syndrome Versus 2 Controls Population
The purpose of this trial is to investigate the impact of cortisol on adipose tissue functions, distribution and morphology. Patient with endogenous blood cortisol excess exhibit changes in adipose tissue, with fat gain in the upper trunk, face and neck leading to visceral obesity and features of the metabolic syndrome. The aims of this study will be
- to compare the pattern of gene expression between visceral and subcutaneous adipose tissue in Cushing patients requiring an adrenalectomy as cortisol adenoma treatment;
- to compare these patterns of gene expression with those of two control populations:1/ healthy metabolic subjects having a partial nephrectomy, 2/obese patients with similar degree of insulin resistance.
Visão geral do estudo
Status
Intervenção / Tratamento
Descrição detalhada
Cushing's syndrome is a rare disease resulting from chronic exposure to glucocorticoids (endogenous or iatrogenic) with abnormal fat distribution (lipodystrophy). Glucocorticoids regulate the functions of adipose tissue (AT) targeting adipocyte differentiation as well as anabolic, catabolic and secretory pathways of the adipocyte. However, the mechanisms by which glucocorticoids differentially disrupt the development or metabolism of AT between deep and superficial deposits remain unknown. Among the main effectors of the glucocorticoid signaling pathway, 11 beta-hydroxysteroid deshydrogenase (11beta-HSD1) , that regenerate cortisol from cortisone, is likely a key step in the biological effect of glucocorticoids in AT. Identifying these mechanisms of action of glucocorticoids on different fat depots requires the comparison with fatty deposits derived from two types of control populations: 1/ normal weight individuals without inflammatory or metabolic disorder (controls1); 2/individuals obese matched for the level of insulin resistance (controls2).
Hypothesis: Excess glucocorticoids cause abnormal fat distribution via a direct effect on the various deposits of AT, leading secondarily to insulin resistance.
Primary endpoint: To compare gene expression of glucocorticoid signaling between the visceral AT (VAT) of Cushing patients with that of controls1 (matched for age and sex).
Secondary endpoints:
For patients with Cushing and controls1, to compare their respective subcutaneous AT (SCAT) and VAT for:
- The expression of genes involved in differentiation and inflammation of the AT,
- Morphological aspects: adipocyte size, fibrosis, inflammation, immunohistochemistry.
- Same parameters for Cushing patients and controls2 (matched for sex, age + / -5, HOMA-R + / -1), to differentiate the specific effects of glucocorticoid from the effects of insulin resistance,
- To compare these parameters between SCAT and VAT from Cushing patients. Methodology and experimental design: non-randomized comparative multicenter study with constitution of a biological collection.
Patients will be recruited in endocrinology before adrenalectomy and controls1 in urology. They will have a preoperative assessment and sampling of perirenal AT and SCAT at surgery. Controls2 are already included in the CRC2007-P050318 and will be drawn for matching.
Number of patients needed: We assume the relative gene expression of 11β-HSD1 in the VAT not exposed to glucocorticoids = 0.81 ± 0.121. Our recruitment potential of Cushing patients is 30 patients. With 30 patients per group, we will be able to detect a difference in 11β-HSD1 gene expression in the VAT of Cushing patients at least 15% higher compared to controls1.
Tipo de estudo
Inscrição (Real)
Estágio
- Não aplicável
Contactos e Locais
Locais de estudo
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Paris, França, 75012
- Hôpital Saint-Antoine, service d'Endocrinologie
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
Inclusion Criteria:
- Cases: Adults with Cushing's syndrome secondary to adrenal adenoma.
- Controls1: Adults with normal weight: BMI <25, having partial nephrectomy
- Controls2 adults with common obesity treated by bariatric surgery, BMI> 35kg/m2
Exclusion Criteria:
- Diabetes, renal or hepatic impairment, pregnancy, menopause, HIV or HCV, Cushing's syndrome due to other causes than cortisol adenoma
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Ciência básica
- Alocação: Não randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Solteiro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
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Experimental: Cushing group
AT biopsy during partial nephrectomy
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The purpose of this trial is to investigate the impact of cortisol on adipose tissue functions, distribution and morphology. Patient with endogenous blood cortisol excess exhibit changes in adipose tissue, with fat gain in the upper trunk, face and neck leading to visceral obesity and features of the metabolic syndrome. The aims of this study will be
|
|
Outro: Controls1
normal weight metabolic healthy patients having partial nephrectomy with small AT Biopsy.
|
The purpose of this trial is to investigate the impact of cortisol on adipose tissue functions, distribution and morphology. Patient with endogenous blood cortisol excess exhibit changes in adipose tissue, with fat gain in the upper trunk, face and neck leading to visceral obesity and features of the metabolic syndrome. The aims of this study will be
|
|
Outro: Controls2
obese individuals already included and having biopsies of VAT and SCAT stocked.
|
The purpose of this trial is to investigate the impact of cortisol on adipose tissue functions, distribution and morphology. Patient with endogenous blood cortisol excess exhibit changes in adipose tissue, with fat gain in the upper trunk, face and neck leading to visceral obesity and features of the metabolic syndrome. The aims of this study will be
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Comparison between visceral adipose tissue of Cushing patients and that of normal weight controls.
Prazo: 1 day (gene expression will be tested on AT withdraw the day of surgical adrenalectomy)
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Comparison of glucocorticoid pathway genes expression between visceral adipose tissue of Cushing patients and that of normal weight controls matched on sex and age.
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1 day (gene expression will be tested on AT withdraw the day of surgical adrenalectomy)
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Comparison of the respective SCAT and VAT between Cushing patients and normal weight controls.
Prazo: 1 day (gene expression will be tested on AT withdraw the day of surgical adrenalectomy)
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For patients with Cushing and controls1, to compare their respective SCAT and VAT for:
|
1 day (gene expression will be tested on AT withdraw the day of surgical adrenalectomy)
|
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Comparison of the respective SCAT and VAT between Cushing patients and obese controls.
Prazo: 1 day (gene expression will be tested on AT withdraw the day of surgical adrenalectomy)
|
Comparison of these same parameters(secondary outcome n°1) between Cushing patients and controls2 (matched for sex, age + / -5, HOMA-R + / -1), to differentiate the specific effects of glucocorticoid from the effects of insulin resistance
|
1 day (gene expression will be tested on AT withdraw the day of surgical adrenalectomy)
|
|
comparison between SCAT and VAT from Cushing patients
Prazo: 1 day (gene expression will be tested on AT withdraw the day of surgical adrenalectomy)
|
To compare these parameters between SCAT and VAT from Cushing patients
|
1 day (gene expression will be tested on AT withdraw the day of surgical adrenalectomy)
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Bruno Feve, PhD, Assistance Publique
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo
Conclusão Primária (Real)
Conclusão do estudo (Real)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Estimativa)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
- Processos Patológicos
- Neoplasias por Tipo Histológico
- Neoplasias
- Neoplasias Glandulares e Epiteliais
- Doenças do Sistema Endócrino
- Doença
- Hiperfunção Adrenocortical
- Doenças da Glândula Adrenal
- Síndrome
- Adenoma
- Síndrome de Cushing
- Efeitos Fisiológicos das Drogas
- Hormônios
- Hormônios, Substitutos Hormonais e Antagonistas Hormonais
- Glicocorticóides
Outros números de identificação do estudo
- P110906
- CRC11001 (Outro identificador: Assistance Publique)
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