对海平面和高海拔地区微剂量促红细胞生成素治疗敏感和特异的 mRNA 生物标志物。

IF 2.6 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS
Francesco Loria, Andreas Breenfeldt Andersen, Jacob Bejder, Thomas Bonne, Silke Grabherr, Tiia Kuuranne, Nicolas Leuenberger, Nikolai Baastrup Nordsborg
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引用次数: 0

摘要

世界反兴奋剂机构禁止使用重组人促红细胞生成素(rhEPO)。然而,高原暴露对 ABP 的解释提出了挑战。本研究调查了毛细管干血斑(DBSs)中的5'-氨基乙酰丙酸合成酶2(ALAS2)和碳酸酐酶1(CA1)是否是在高海拔地区接受rhEPO治疗的敏感而特异的标志物。在海平面或高海拔地区进行为期 3 周的治疗之前、期间和之后,每周采集的毛细血管干血斑中的 ALAS2 和 CA1 表达情况都会受到监测。参与者被随机分配到海平面(rhEPO,n = 25;安慰剂,n = 9)或高海拔(rhEPO,n = 12;安慰剂,n = 27)环境中,连续3周每隔一天接受20 IU kg bw-1 的epoetin alpha(rhEPO)或安慰剂注射。在海平面和高海拔地区接受rhEPO治疗后,ALAS2和CA1的表达量分别增加了300%和200%(P值
本文章由计算机程序翻译,如有差异,请以英文原文为准。
mRNA biomarkers sensitive and specific to micro-dose erythropoietin treatment at sea level and altitude

Recombinant human erythropoietin (rhEPO) is prohibited by the World Anti-Doping Agency. rhEPO abuse can be indirectly detected via the athlete biological passport (ABP). However, altitude exposure challenges interpretation of the ABP. This study investigated whether 5′-aminolevulinate synthase 2 (ALAS2) and carbonic anhydrase 1 (CA1) in capillary dried blood spots (DBSs) are sensitive and specific markers of rhEPO treatment at altitude. ALAS2 and CA1 expression was monitored in DBS collected weekly before, during, and after a 3-week period at sea level or altitude. Participants were randomly assigned to receive 20 IU kg bw−1 epoetin alpha (rhEPO) or placebo injections every second day for 3 weeks while staying at sea level (rhEPO, n = 25; placebo, n = 9) or altitude (rhEPO, n = 12; placebo, n = 27). ALAS2 and CA1 expression increased up to 300% and 200%, respectively, upon rhEPO treatment at sea-level and altitude (P-values <0.05). When a blinded investigator interpreted the results, ALAS2 and CA1 expression had a sensitivity of 92%. Altitude did not confound the interpretation. Altitude affected ALAS2 and CA1 expression less than actual ABP markers when compared between sea level and altitude results. An individual athlete passport-like approach simulation confirmed the biomarker potential of ALAS2 and CA1. ALAS2 and CA1 were sensitive and specific biomarkers of micro-dose rhEPO treatment at sea level and altitude. Altitude seemed less a confounding factor for these biomarkers, especially when they are combined. Thus, micro-dose rhEPO injections can be detected in a longitudinal blinded setting using mRNA biomarkers in DBS.

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来源期刊
Drug Testing and Analysis
Drug Testing and Analysis BIOCHEMICAL RESEARCH METHODS-CHEMISTRY, ANALYTICAL
CiteScore
5.90
自引率
24.10%
发文量
191
审稿时长
2.3 months
期刊介绍: As the incidence of drugs escalates in 21st century living, their detection and analysis have become increasingly important. Sport, the workplace, crime investigation, homeland security, the pharmaceutical industry and the environment are just some of the high profile arenas in which analytical testing has provided an important investigative tool for uncovering the presence of extraneous substances. In addition to the usual publishing fare of primary research articles, case reports and letters, Drug Testing and Analysis offers a unique combination of; ‘How to’ material such as ‘Tutorials’ and ‘Reviews’, Speculative pieces (‘Commentaries’ and ‘Perspectives'', providing a broader scientific and social context to the aspects of analytical testing), ‘Annual banned substance reviews’ (delivering a critical evaluation of the methods used in the characterization of established and newly outlawed compounds). Rather than focus on the application of a single technique, Drug Testing and Analysis employs a unique multidisciplinary approach to the field of controversial compound determination. Papers discussing chromatography, mass spectrometry, immunological approaches, 1D/2D gel electrophoresis, to name just a few select methods, are welcomed where their application is related to any of the six key topics listed below.
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