当保存在不理想和不受控制的温度和湿度条件下,剩余的新生儿筛查标本对重新检测有用多长时间?

Q3 Medicine
G. Borrajo, V. Doña
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引用次数: 2

摘要

收集1995-2018年诊断为苯丙酮尿症、先天性甲状腺功能减退症、囊性纤维化症、先天性肾上腺增生症和半乳糖血症的新生儿DBS残余标本,在无控制条件下室温保存于纸箱中,重新检测苯丙氨酸(Phe)、促甲状腺素(TSH)、免疫反应性胰蛋白酶原(IRT)、总半乳糖(TGal)和17-羟基孕酮(17OHP)的含量。为了证明它们在这些条件下稳定多久,并有助于再次确认先前的异常结果。评估了重测时的回收率和当前截止点的定性解释。随着时间的推移,Phe、TSH和IRT的恢复呈下降趋势。储存2年后Phe回收率为64%;TSH快速衰减,1年恢复47.3%,而IRT 1年恢复60%。尽管17OHP采收率的结果变化很大,但也发现了衰减趋势。结果表明,17OHP比TSH和IRT更稳定,当储存≤2年时,回收率> 71%。总回收率表现出不稳定的行为,因此不可能估计预期浓度作为储存时间的函数。在缺乏udp -半乳糖-4- epimase和半乳糖-1-磷酸尿苷转移酶的情况下,发现半乳糖回收率超过100%,证明可能有其他来源的半乳糖释放。这些结果为在非受控条件下存储残余DBS的程序做出了非常有价值的贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
How Long are Residual Newborn Screening Specimens Useful for Retesting when Stored in Suboptimal and Uncontrolled Conditions of Temperature and Humidity?
Abstract Residual DBS specimens from newborns diagnosed with Phenylketonuria, Congenital Hypothyroidism, Cystic Fibrosis, Congenital Adrenal Hyperplasia and Galactosemia collected within 1995-2018, stored in cardboard boxes at ambient temperature in uncontrolled conditions, were retested for phenylalanine (Phe), thyrotropin (TSH), immunoreactive trypsinogen (IRT), total galactose (TGal) and 17-hydroxyprogesterone (17OHP), to demonstrate how long are they stable in these conditions and useful to reconfirm a previous abnormal result. Recovery percentage at retesting and qualitative interpretation regarding the current cutoff were evaluated. Phe, TSH and IRT recoveries showed decreasing trends along time. Phe recovery was 64 % after 2-years storage; TSH decayed rapidly recovering 47.3 % at 1-year, while IRT showed recoveries of 60 % at 1-year. Although 17OHP recovery presented a wide variation of results, a decaying trend was also found. Results suggest 17OHP is more stable than TSH and IRT, as supported by recoveries > 71 % when stored ≤ 2-years. TGal recovery presented an erratic behavior, so that it was not possible to estimate expected concentrations as a function of storage time. TGal recoveries above 100 % were found in UDP-galactose-4-epimerase and galactose-1-phosphate uridyltransferase deficiencies, evidencing possible galactose liberation from other sources. These results make a very valuable contribution for programs storing residual DBS in uncontrolled conditions.
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来源期刊
CiteScore
0.60
自引率
0.00%
发文量
7
审稿时长
12 weeks
期刊介绍: The Journal of Inborn Errors of Metabolism and Screening (JIEMS) is an online peer-reviewed open access journal devoted to publishing clinical and experimental research in inherited metabolic disorders and screening, for health professionals and scientists. Original research articles published in JIEMS range from basic findings that have implications for disease pathogenesis and therapy, passing through diagnosis and screening of metabolic diseases and genetic conditions, and therapy development and outcomes as well. Original articles, reviews on specific topics, brief communications and case reports are welcome. JIEMS aims to become a key resource for geneticists, genetic counselors, biochemists, molecular biologists, reproductive medicine researchers, obstetricians/gynecologists, neonatologists, pediatricians, pathologists and other health professionals interested in inborn errors of metabolism and screening.
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