van de Laak Marielle F, Grobbee Diederick E, van der Griend Rene, de Valk Harold W, Algra Ale, Banga Jan-Dirk, van der Graaf Yolanda
Julius Center for Health Sciences and Primary Care University Medical Center Utrecht, The Netherland.
J Lab Clin Med. 2003 Aug;142(2):121-7. doi: 10.1016/S0022-2143(03)00103-3.
An increased plasma homocysteine level may increase the risk of cardiovascular disease. The methionine-loading test is commonly used to detect additional subjects with hyperhomocysteinemia who have normal fasting levels of homocysteine but increased post-methionine-load levels. We developed a 2-step strategy to restrict the methionine-loading test to those subjects with intermediate fasting homocysteine levels to confirm the presence of hyperhomocysteinemia. Hyperhomocysteinemia was defined as a fasting plasma homocysteine level of 16.3 micro mol/L or greater in women and 18.8 micro mol/L or greater in men or an increase in plasma homocysteine level after methionine loading of more than 42.3 micro mol/L for both sexes. From the results in 201 patients, 50 years and younger, with manifest atherosclerosis who underwent a methionine-loading test, we derived cutoff points to define an intermediate group of patients who required a methionine-loading test for hyperhomocysteinemia to be ruled out. These cutoff points were validated in a different population of 275 cardiovascular patients of similar age. The prevalence of hyperhomocysteinemia was 30% in the derivation population and 24% in the validation population. To achieve a sensitivity of 90% in diagnosing hyperhomocysteinemia, we set cutoff points of 11.3 and 9.4 micro mol/L for men and women, respectively. When these cutoff points are applied, it is possible to avoid performing the methionine-loading test in 50% to 75% of subjects tested. With a 2-step strategy to diagnose hyperhomocysteinemia, a sensitivity of 90% for the diagnosis of hyperhomocysteinemia can be achieved, and the need for the methionine-loading test is reduced substantially, with 50% to 75% of subjects no longer needing it.
血浆同型半胱氨酸水平升高可能会增加心血管疾病的风险。蛋氨酸负荷试验通常用于检测空腹同型半胱氨酸水平正常但蛋氨酸负荷后水平升高的高同型半胱氨酸血症患者。我们制定了一种两步策略,将蛋氨酸负荷试验限制在空腹同型半胱氨酸水平处于中间值的受试者中,以确认是否存在高同型半胱氨酸血症。高同型半胱氨酸血症的定义为:女性空腹血浆同型半胱氨酸水平为16.3微摩尔/升或更高,男性为18.8微摩尔/升或更高;或男女两性蛋氨酸负荷后血浆同型半胱氨酸水平升高超过42.3微摩尔/升。从201名50岁及以下患有明显动脉粥样硬化且接受了蛋氨酸负荷试验的患者的结果中,我们得出了切点,以定义一组中间患者,这些患者需要进行蛋氨酸负荷试验以排除高同型半胱氨酸血症。这些切点在年龄相似的275名心血管疾病患者的不同人群中得到了验证。推导人群中高同型半胱氨酸血症的患病率为30%,验证人群中为24%。为了在诊断高同型半胱氨酸血症时达到90%的灵敏度,我们分别将男性和女性的切点设定为11.3微摩尔/升和9.4微摩尔/升。当应用这些切点时,有可能避免在50%至75%的受试对象中进行蛋氨酸负荷试验。采用两步策略诊断高同型半胱氨酸血症,可实现90%的诊断灵敏度,并且蛋氨酸负荷试验的需求大幅减少,50%至75%的受试者不再需要该试验。