Cardiac Amyloidosis in Aging African Americans
老年非裔美国人的心脏淀粉样变性
基本信息
- 批准号:6321660
- 负责人:
- 金额:$ 56.39万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2001
- 资助国家:美国
- 起止时间:2001-07-01 至 2006-06-30
- 项目状态:已结题
- 来源:
- 关键词:African American age difference amyloidosis cardiovascular disorder epidemiology clinical research comorbidity congenital cardiovascular disorder congestive heart failure diagnosis design /evaluation disease /disorder etiology electrocardiography genetic markers genetic polymorphism genetic screening genetic susceptibility heterozygote human genetic material tag human mortality human old age (65+) human subject nucleic acid sequence patient care planning racial /ethnic difference serum albumin statistics /biometry
项目摘要
DESCRIPTION (Verbatim from the application): If factors related to access to
care are not considered, the increased mortality from cardiovascular disease in
African-Americans relative to other groups is due to the increased frequency of
some diseases, a qualitatively different cardiac response to disorders
affecting all ethnic groups and a relatively poor response to treatment of
congestive heart failure. An undiagnosed, coexistent, relatively prevalent,
treatment-resistant cardiomyopathy is a possible partial explanation. Late
onset amyloidotic cardiomyopathy is fourfold more common in African-Americans
than Caucasians. It causes congestive heart failure and arrhythmias, however
these features are relatively non-specific and the clinical diagnosis is not
always obvious. Digoxin and calcium channel blockers are toxic in patients with
amyloid, thus, treatment of concomitant heart disease of other etiologies may
be compromised; moreover misdiagnosis of amyloid heart disease may result in
possibly harmful therapy. Unrecognized amyloidosis, in individuals over age 60,
could contribute to some of the refractoriness seen in studies of congestive
heart failure and to the higher cardiovascular morbidity and mortality in
African-Americans.
Our proposal examines a genetically determined form of late-onset amyloidosis
due to a substitution of ILE for VAL at position 122 in the serum protein
transthyretin (TTR). Approximately 4% of African-Americans are heterozygous for
the allele that has an absolute risk for anatomic amyloid deposition after age
60 resulting in 154,000 African-Americans with some degree of cardiac
amyloidosis. In a collaborative effort with two studies of cardiovascular risk
in the community (ARIC and CFIS), with a combined African-American cohort of
5200, we will test the hypothesis that heterozygosity for the amyloidogenic
allele is associated with clinical evidence of cardiac amyloidosis and a
related increase in mortality. We will also assess the role of the allele in
clinical heart disease by determining its prevalence in a cohort of
African-American veterans, over 60, who are recognized as having heart disease,
although their providers have not considered amyloidosis as a specific
diagnosis. We will characterize the natural history of late onset cardiac
amyloidosis in African-Americans, define its role in cardiovascular morbidity
and mortality in this ethnic group and define guidelines for supportive
treatment at present and specific therapy when available.
描述(来自申请的逐字描述):如果与获得
不考虑护理,心血管疾病的死亡率增加,
非洲裔美国人相对于其他群体的增加是由于
一些疾病,对疾病的心脏反应有质的不同,
影响到所有种族群体,
充血性心力衰竭一种未确诊的,共存的,相对普遍的,
难治性心肌病是一种可能的部分解释。晚
非裔美国人中淀粉样心肌病发病率是
比高加索人。然而,它会导致充血性心力衰竭和心律失常,
这些特征是相对非特异性的,
总是显而易见的。地高辛和钙通道阻滞剂在以下患者中具有毒性:
因此,淀粉样蛋白治疗其他病因的伴随心脏病可
此外,淀粉样心脏病的误诊可能导致
可能有害的治疗不明淀粉样变性,在60岁以上的人,
可能导致充血性心力衰竭研究中观察到的一些不应性,
心力衰竭和较高的心血管发病率和死亡率,
非裔美国人
我们的提案检查了由基因决定的迟发性淀粉样变性形式
由于血清蛋白中122位的瓦尔被ILE取代
甲状腺素运载蛋白(TTR)。大约4%的非洲裔美国人是杂合子,
该等位基因在年龄增长后具有淀粉样蛋白沉积的绝对风险
60导致154,000名非洲裔美国人患有某种程度的心脏病
淀粉样变性在两项关于心血管风险的研究中,
在社区(ARIC和CFIS),与非洲裔美国人的组合队列,
5200,我们将检验淀粉样蛋白基因的杂合性
等位基因与心脏淀粉样变性的临床证据相关,
相关死亡率上升。我们还将评估等位基因在以下方面的作用:
通过确定其在一个队列中的患病率,
60岁以上的非裔美国退伍军人被认为患有心脏病,
尽管他们的提供者还没有将淀粉样变性视为一种特异性的
诊断.我们将描述迟发性心脏病的自然史
非裔美国人的淀粉样变性,确定其在心血管发病率中的作用
和死亡率,并确定支持性的指导方针,
目前的治疗和具体的治疗时,可用的。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Joel N Buxbaum其他文献
Joel N Buxbaum的其他文献
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{{ truncateString('Joel N Buxbaum', 18)}}的其他基金
Cardiac Amyloidosis in Aging African American
老年非洲裔美国人的心脏淀粉样变性
- 批准号:
8333471 - 财政年份:2011
- 资助金额:
$ 56.39万 - 项目类别:
Stimulators of Neuronal Transthyretin (TTR) Transcription as Alzheimer's Therapy
神经元运甲状腺素蛋白 (TTR) 转录刺激剂用于治疗阿尔茨海默病
- 批准号:
8331502 - 财政年份:2011
- 资助金额:
$ 56.39万 - 项目类别:
Stimulators of Neuronal Transthyretin (TTR) Transcription as Alzheimer's Therapy
神经元运甲状腺素蛋白 (TTR) 转录刺激剂用于治疗阿尔茨海默病
- 批准号:
8228211 - 财政年份:2011
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$ 56.39万 - 项目类别:
Aging and the Tissue Response to Misfolded Proteins
衰老和组织对错误折叠蛋白质的反应
- 批准号:
7906579 - 财政年份:2009
- 资助金额:
$ 56.39万 - 项目类别:
Aging and the Tissue Response to Misfolded Proteins
衰老和组织对错误折叠蛋白质的反应
- 批准号:
8240431 - 财政年份:2008
- 资助金额:
$ 56.39万 - 项目类别:
Aging and the Tissue Response to Misfolded Proteins
衰老和组织对错误折叠蛋白质的反应
- 批准号:
7795125 - 财政年份:2008
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$ 56.39万 - 项目类别:
Aging and the Tissue Response to Misfolded Proteins
衰老和组织对错误折叠蛋白质的反应
- 批准号:
8054410 - 财政年份:2008
- 资助金额:
$ 56.39万 - 项目类别:
Aging and the Tissue Response to Misfolded Proteins
衰老和组织对错误折叠蛋白质的反应
- 批准号:
7586153 - 财政年份:2008
- 资助金额:
$ 56.39万 - 项目类别:
Aging and the Tissue Response to Misfolded Proteins
衰老和组织对错误折叠蛋白质的反应
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