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首页> 外文期刊>Molecular Genetics and Metabolism Reports >Targeted screening of succinic semialdehyde dehydrogenase deficiency (SSADHD) employing an enzymatic assay for γ-hydroxybutyric acid (GHB) in biofluids
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Targeted screening of succinic semialdehyde dehydrogenase deficiency (SSADHD) employing an enzymatic assay for γ-hydroxybutyric acid (GHB) in biofluids

机译:使用酶法测定生物流体中的γ-羟基丁酸(GHB),以靶向筛选琥珀酸半醛脱氢酶缺乏症(SSADHD)

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Hypothesis An enzymatic assay for quantification of γ-hydroxybutyric acid (GHB) in biofluids can be employed for targeted screening of succinic semialdehyde dehydrogenase deficiency (SSADHD) in selected populations. Rationale We used a two-tiered study approach, in which the first study (proof of concept) examined 7 urine samples derived from patients with SSADHD and 5 controls, and the second study (feasibility study) examined a broader sample population of patients and controls, including plasma. Objective Split samples of urine and plasma (anonymized) were evaluated by enzymatic assay, gas chromatography alone (proof of concept) and gas chromatography–mass spectrometry, and the results compared. Method Multiple detection methods have been developed to detect GHB. We evaluated an enzymatic assay which employs recombinant GHB dehydrogenase coupled to NADH production, the latter quantified on a Cobas Integra 400 Plus. Results: In our proof of concept study, we analyzed 12 urine samples (5 controls, 7 SSADHD), and in the feasibility study we evaluated 33 urine samples (23 controls, 10 SSADHD) and 31 plasma samples (14 controls, 17 SSADHD). The enzymatic assay carried out on a routine clinical chemistry analyzer was robust, revealing excellent agreement with instrumental methods in urine (GC-FID: r = 0.997, p ≤ 0.001; GC–MS: r = 0.99, p ≤ 0.001); however, the assay slightly over-estimated GHB levels in plasma, especially those in which GHB levels were low. Conversely, correlations for the enzymatic assay with comparator methods for higher plasma GHB levels were excellent (GC–MS; r = 0.993, p ≤ 0.001). Conclusion We have evaluated the capacity of this enzymatic assay to identify patients with SSADHD via quantitation of GHB. The data suggests that the enzymatic assay may be a suitable screening method to detect SSADHD in selected populations using urine. In addition, the assay can be used in basic research the elucidate the mechanism of the underlying disease or monitor GHB- levels for the evaluation of drug candidates. Synopsis An enzymatic assay for GHB in biofluids was evaluated as a screening method for SSADHD and found to be reliable in urine, but in need of refinement for application to plasma.
机译:假设一种用于定量生物流体中γ-羟基丁酸(GHB)的酶法可用于靶向筛选选定人群中的琥珀酸半醛脱氢酶缺乏症(SSADHD)。原理我们采用了两层研究方法,其中第一项研究(概念验证)检查了7名来自SSADHD患者和5名对照的尿液样本,第二项研究(可行性研究)检查了更广泛的患者和对照组样本,包括血浆。目的通过酶法,气相色谱法(概念验证)和气相色谱-质谱法对尿液和血浆的分离样品(匿名)进行评估,并将结果进行比较。方法已经开发出多种检测方法来检测GHB。我们评估了使用重组GHB脱氢酶与NADH生产偶联的酶促测定,后者在Cobas Integra 400 Plus上进行了定量。结果:在概念验证研究中,我们分析了12个尿液样本(5个对照,7个SSADHD),在可行性研究中,我们评估了33个尿液样本(23个对照,10个SSADHD)和31个血浆样品(14个对照,17个SSADHD)。 。在常规的临床化学分析仪上进行的酶促测定非常可靠,与尿液中的仪器方法显示出极好的一致性(GC-FID:r = 0.997,p≤0.001; GC-MS:r = 0.99,p≤0.001);但是,该测定法略高估了血浆中的GHB水平,尤其是那些GHB水平较低的血浆。相反,酶促测定法与比较法测定血浆GHB较高的相关性极好(GC-MS; r = 0.993,p≤0.001)。结论我们评估了这种酶法通过定量GHB鉴定SSADHD患者的能力。数据表明,酶法检测可能是检测尿液中选定人群SSADHD的合适筛选方法。另外,该测定可用于基础研究,阐明潜在疾病的机制或监测GHB-水平,以评估候选药物。提要评估了生物流体中GHB的酶法检测方法作为SSADHD的筛选方法,发现在尿液中是可靠的,但需要改进以应用于血浆。

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