The role of Homocysteine as a predictor for coronary heart disease.

GMS health technology assessment Pub Date : 2007-11-09
Dagmar Lühmann, Susanne Schramm, Heiner Raspe
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In order to use this information for the construction of a new preventive strategy against coronary heart disease, more information is needed: first, whether homocysteine actually is a causal risk factor with relevant predictive properties and, second, whether by lowering elevated homocysteine plasma concentrations cardiac morbidity can be reduced. Currently in Germany the determination of homocysteine plasma levels is reimbursed for by statutory health insurance in patients with manifest coronary heart disease and in patients at high risk for coronary heart disease but not for screening purposes in asymptomatic low risk populations. Against this background the following assessment sets out to answer four questions: Is an elevated homocysteine plasma concentration a strong, consistent and independent (of other classic risk factors) predictor for coronary heart disease?Does a therapeutic lowering of elevated homoysteine plasma levels reduce the risk of developing coronary events?What is the cost-effectiveness relationship of homocysteine testing for preventive purposes?Are there morally, socially or legally relevant aspects that should be considered when implementing a preventive strategy as outlined above?</p><p><strong>Methods: </strong>In order to answer the first question, a systematic overview of prospective studies and metaanalyses of prospective studies is undertaken. Studies are included that analyse the association of homocysteine plasma levels with future cardiac events in probands without pre-existing coronary heart disease or in population-based samples. 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Taking these heterogeneities into consideration, metaanalysis of single patient data with controlling for multiple confounders seems to be the only adequate method of summarizing the results of single studies. The only available analysis of this type shows, that in otherwise healthy people homocysteine plasma levels are only a very weak predictor of future cardiac events. The predictive value of the classical risk factors is much stronger. Among the studies that actively exclude patients with pre-existing coronary heart disease, there are no reports of an association between elevated homocysteine plasma levels and future cardiac events. Eleven randomized controlled trials (ten of them reported in one systematic review) are analysed in order to answer the second question. All trials include high risk populations for the development of (further) cardiac events. These studies also present with marked clinical heterogeneity: primarily concerning the average homocysteine plasma levels at baseline, type and mode of outcome measurement and as study duration. Except for one, none of the trials shows a risk reduction for cardiac events by lowering homocysteine plasma levels with folate or B vitamins. These results also hold for predefined subgroups with markedly elevated homocysteine plasma levels. In order to answer the third questions, three economic evaluations (modelling studies) of homocysteine testing are available. All economic models are based on the assumption that lowering homocysteine plasma levels results in risk reduction for cardiac events. Since this assumption is falsified by the results of the interventional studies cited above, there is no evidence left to answer the third question. Morally, socially or legally relevant aspects of homocysteine assessment are currently not being discussed in the scientific literature.</p><p><strong>Discussion and conclusion: </strong>Many currently available pieces of evidence contradict a causal role of homocysteine in the pathogenesis of coronary heart disease. Arguing with the Bradford-Hill criteria at least the criterion of time-sequence (that exposure has to happen before the outcome is measured), the criterion of a strong and consistent association and the criterion of reversibility are not fulfilled. Therefore, homocysteine may, if at all, play a role as a risk indicator but not as risk factor. Furthermore, currently available evidence does not imply that for the prevention of coronary heart disease, knowledge of homocysteine plasma levels provides any information that supersedes the information gathered from the examination of classical risk factors. 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引用次数: 0

Abstract

Background and objective: There is an ongoing debate on the role of the cytotoxic aminoacid homocysteine as a causal risk factor for the development of coronary heart disease. Results from multiple case control-studies demonstrate, that there is a strong association between high plasma levels of homoysteine and prevalent coronary heart disease, independent of other classic risk factors. Furthermore, results from interventional studies point out that elevated plasma levels of homocysteine may effectively be lowered by the intake of folic acid and B vitamins. In order to use this information for the construction of a new preventive strategy against coronary heart disease, more information is needed: first, whether homocysteine actually is a causal risk factor with relevant predictive properties and, second, whether by lowering elevated homocysteine plasma concentrations cardiac morbidity can be reduced. Currently in Germany the determination of homocysteine plasma levels is reimbursed for by statutory health insurance in patients with manifest coronary heart disease and in patients at high risk for coronary heart disease but not for screening purposes in asymptomatic low risk populations. Against this background the following assessment sets out to answer four questions: Is an elevated homocysteine plasma concentration a strong, consistent and independent (of other classic risk factors) predictor for coronary heart disease?Does a therapeutic lowering of elevated homoysteine plasma levels reduce the risk of developing coronary events?What is the cost-effectiveness relationship of homocysteine testing for preventive purposes?Are there morally, socially or legally relevant aspects that should be considered when implementing a preventive strategy as outlined above?

Methods: In order to answer the first question, a systematic overview of prospective studies and metaanalyses of prospective studies is undertaken. Studies are included that analyse the association of homocysteine plasma levels with future cardiac events in probands without pre-existing coronary heart disease or in population-based samples. To answer the second question, a systematic overview of the literature is prepared, including randomised controlled trials and systematic reviews of randomised controlled trials that determine the effectiveness of homocysteine lowering therapy for the prevention of cardiac events. To answer the third question, economic evaluations of homocysteine testing for preventive purposes are analysed. Methodological quality of all materials is assessed by widely accepted instruments, evidence was summarized qualitatively.

Results: For the first question eleven systematic reviews and 33 single studies (prospective cohort studies and nested case control studies) are available. Among the studies there is profound heterogeneity concercing study populations, classification of exposure (homocysteine measurements, units to express "elevation"), outcome definition and measurement, as well as controlling for confounding (qualitatively and quantitatively). Taking these heterogeneities into consideration, metaanalysis of single patient data with controlling for multiple confounders seems to be the only adequate method of summarizing the results of single studies. The only available analysis of this type shows, that in otherwise healthy people homocysteine plasma levels are only a very weak predictor of future cardiac events. The predictive value of the classical risk factors is much stronger. Among the studies that actively exclude patients with pre-existing coronary heart disease, there are no reports of an association between elevated homocysteine plasma levels and future cardiac events. Eleven randomized controlled trials (ten of them reported in one systematic review) are analysed in order to answer the second question. All trials include high risk populations for the development of (further) cardiac events. These studies also present with marked clinical heterogeneity: primarily concerning the average homocysteine plasma levels at baseline, type and mode of outcome measurement and as study duration. Except for one, none of the trials shows a risk reduction for cardiac events by lowering homocysteine plasma levels with folate or B vitamins. These results also hold for predefined subgroups with markedly elevated homocysteine plasma levels. In order to answer the third questions, three economic evaluations (modelling studies) of homocysteine testing are available. All economic models are based on the assumption that lowering homocysteine plasma levels results in risk reduction for cardiac events. Since this assumption is falsified by the results of the interventional studies cited above, there is no evidence left to answer the third question. Morally, socially or legally relevant aspects of homocysteine assessment are currently not being discussed in the scientific literature.

Discussion and conclusion: Many currently available pieces of evidence contradict a causal role of homocysteine in the pathogenesis of coronary heart disease. Arguing with the Bradford-Hill criteria at least the criterion of time-sequence (that exposure has to happen before the outcome is measured), the criterion of a strong and consistent association and the criterion of reversibility are not fulfilled. Therefore, homocysteine may, if at all, play a role as a risk indicator but not as risk factor. Furthermore, currently available evidence does not imply that for the prevention of coronary heart disease, knowledge of homocysteine plasma levels provides any information that supersedes the information gathered from the examination of classical risk factors. So, currently for the indication of prevention, there is no evidence that homocysteine testing provides any benefit. Against this background there is also no basis for cost-effectiveness calculations. Further basic research should clarify the discrepant results of case control studies and prospective studies. Maybe there is a third parameter (confounder) associated with homocysteine metabolism as well with coronary heart disease. Further epidemiological research could elucidate the role of elevated homocysteine plasma levels as a risk indicator or prognostic indicator in patients with pre-existing coronary heart disease taking into consideration the classical risk factors.

同型半胱氨酸作为冠心病预测因子的作用。
背景和目的:关于细胞毒性氨基酸同型半胱氨酸作为冠心病发生的一个因果危险因素的作用,一直存在争论。多个病例对照研究的结果表明,高血浆同型半胱氨酸水平与流行冠心病之间存在很强的关联,独立于其他经典危险因素。此外,介入性研究的结果指出,血浆中升高的同型半胱氨酸水平可以通过摄入叶酸和B族维生素有效地降低。为了利用这些信息构建新的冠心病预防策略,需要更多的信息:首先,同型半胱氨酸是否真的是一个具有相关预测特性的因果危险因素,其次,是否可以通过降低升高的同型半胱氨酸血浆浓度来降低心脏发病率。目前在德国,检测同型半胱氨酸血浆水平由法定健康保险报销,报销对象为明显冠心病患者和冠心病高风险患者,但不用于无症状低风险人群的筛查目的。在此背景下,以下评估旨在回答四个问题:血浆同型半胱氨酸浓度升高是冠心病的一个强有力的、一致的和独立的(其他经典危险因素)预测因子吗?治疗性降低升高的血浆同型半胱氨酸水平能降低发生冠状动脉事件的风险吗?同型半胱氨酸检测用于预防目的的成本-效果关系是什么?在执行上述预防战略时,是否应考虑道德、社会或法律方面的相关问题?方法:为了回答第一个问题,对前瞻性研究进行了系统的概述和前瞻性研究的荟萃分析。研究包括分析无冠心病先证者或基于人群的样本中同型半胱氨酸血浆水平与未来心脏事件的关系。为了回答第二个问题,我们准备了一个系统的文献综述,包括随机对照试验和随机对照试验的系统综述,这些试验确定了降低同型半胱氨酸治疗预防心脏事件的有效性。为了回答第三个问题,分析了同型半胱氨酸检测用于预防目的的经济评价。所有材料的方法学质量由广泛接受的工具进行评估,证据进行定性总结。结果:对于第一个问题,有11个系统综述和33个单一研究(前瞻性队列研究和嵌套病例对照研究)。在这些研究中,在研究人群、暴露分类(同型半胱氨酸测量、表达“升高”的单位)、结果定义和测量以及混杂因素控制(定性和定量)方面存在深刻的异质性。考虑到这些异质性,在控制多个混杂因素的情况下对单个患者数据进行荟萃分析似乎是总结单个研究结果的唯一适当方法。对这种类型的唯一可用分析表明,在健康人群中,同型半胱氨酸血浆水平对未来心脏事件的预测作用非常弱。经典危险因素的预测价值要强得多。在积极排除已有冠心病患者的研究中,没有报道血浆同型半胱氨酸水平升高与未来心脏事件之间存在关联。为了回答第二个问题,我们分析了11个随机对照试验(其中10个在一个系统综述中报道)。所有的试验都包括发生(进一步)心脏事件的高危人群。这些研究也表现出明显的临床异质性:主要涉及基线时的平均同型半胱氨酸血浆水平、结果测量的类型和模式以及研究持续时间。除了一项试验外,没有一项试验显示叶酸或B族维生素能降低血浆中同型半胱氨酸水平,从而降低心脏事件的风险。这些结果也适用于同型半胱氨酸血浆水平显著升高的预定义亚组。为了回答第三个问题,同型半胱氨酸测试的三个经济评估(建模研究)是可用的。所有的经济模型都是基于降低同型半胱氨酸血浆水平导致心脏事件风险降低的假设。由于上述介入研究的结果证明了这一假设是错误的,因此没有证据可以回答第三个问题。同型半胱氨酸评估的道德、社会或法律相关方面目前尚未在科学文献中进行讨论。 讨论和结论:许多现有的证据反驳了同型半胱氨酸在冠心病发病机制中的因果作用。与Bradford-Hill标准相比,至少时间序列标准(暴露必须在测量结果之前发生),强一致关联标准和可逆性标准没有得到满足。因此,同型半胱氨酸如果存在的话,可能只是一种风险指标,而不是风险因素。此外,目前可获得的证据并不意味着,对同型半胱氨酸血浆水平的了解可以提供任何信息,取代从经典危险因素检查中收集到的信息。所以,目前对于预防的指征,没有证据表明同型半胱氨酸检测能提供任何好处。在这种背景下,也没有成本效益计算的基础。进一步的基础研究应澄清病例对照研究和前瞻性研究结果的差异。也许还有第三个参数(混杂因素)与同型半胱氨酸代谢以及冠心病有关。进一步的流行病学研究可以在考虑经典危险因素的情况下,阐明血浆同型半胱氨酸水平升高作为既存冠心病患者的危险指标或预后指标的作用。
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