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Endocrine Abnormalities in Hereditary Disorders of Connective Tissue

Endocrine Abnormalities in Hereditary Disorders of Connective Tissue
结缔组织遗传性疾病的内分泌异常
批准号:
8552498
负责人:
Nazli Mcdonnell
金额:
$10.16万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至

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中文摘要
翻译
我们分析了参加IRB批准的2003-086方案的大约200名参与者的血浆样本,这些患者被诊断为埃勒斯-丹洛斯综合征、纤维肌肉发育不良和马凡综合征。这些诊断与不良心血管事件和导致过早死亡的早期血管老化有关。感兴趣的内分泌标志物包括游离和总睾酮、性激素结合球蛋白、雌酮、雌二醇、IGF-1、黄体生成素和卵泡刺激素。大约30%患有埃勒斯-丹洛斯综合征和马凡综合征的男性睾酮水平异常低下。相应的黄体生成素和卵泡刺激素水平较低,表明垂体腺功能异常,而不是性腺功能障碍。性激素结合球蛋白升高见于女性,将以上所有诊断。结缔组织疾病儿童的IGF-1循环值较低。此外,与年龄和性别匹配的对照组相比,脉管型Ehler Danlos患者的瘦素水平升高。内分泌异常与骨密度降低和心血管预后不良有关。我们计划研究这些发现的病理机制。目前尚不清楚这些异常是否是对潜在血管病理的保护性反应,而不是与不良血管事件的发展相关的因果关系。纠正这些异常的决定取决于对这些发现的机制的更好理解。
英文摘要
We have analyzed plasma samples from approximately 200 of the participants enrolled in IRB-approved protocol 2003-086 with diagnoses of Ehlers Danlos Syndrome, Fibromuscular Dysplasia and Marfan Syndrome. These diagnoses are associated with adverse cardiovascular events and early vascular aging causing premature death. The endocrine markers of interest include free and total testosterone, sex hormone binding globulin, estrone, estrodiol, IGF-1, LH and FSH. Approximately 30% of men with Ehlers Danlos syndrome and Marfan syndrome have abnormally low testosterone levels. Corresponding LH and FSH values are low, indicating abnormal pituitary function as opposed to gonadal dysfunction. Elevated Sex Hormone Binding Globulin is seen in women will all the above diagnoses. Children with connective tissue disorders have low circulating values of IGF-1. In addition, patients with the vascular form of Ehlers Danlos have elevated leptin levels as compared to age and sex matched controls. The endocrine abnormalities are correlated with low bone density and poor cardiovascular prognosis. We plan to investigate the pathological mechanisms of these findings. It is not yet clear that these abnormalities are protective responses to the underlying vascular pathology versus causally involved in the development of the adverse vascular events. The decision to correct the abnormalities is dependent on better understanding of the mechanisms of these findings.
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Genetics of Fibromuscular Dysplasia
  • 批准号:
    8552497
  • 项目类别:
  • 资助金额:
    $24.41万
  • 财政年份:
    --
  • 负责人:
    Nazli Mcdonnell
  • 依托单位:
Proteomics and Gene Expression in Hereditary Disorders of Connective Tissue
  • 批准号:
    8335950
  • 项目类别:
  • 资助金额:
    $16.25万
  • 财政年份:
    --
  • 负责人:
    Nazli Mcdonnell
  • 依托单位:
Genetics of Stickler Syndrome
  • 批准号:
    8335951
  • 项目类别:
  • 资助金额:
    $11.61万
  • 财政年份:
    --
  • 负责人:
    Nazli Mcdonnell
  • 依托单位:
Neurological Aspects of Hereditary Disorders of Connective Tissue
  • 批准号:
    8552500
  • 项目类别:
  • 资助金额:
    $13.11万
  • 财政年份:
    --
  • 负责人:
    Nazli Mcdonnell
  • 依托单位:
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