Suppr超能文献

使用干血斑对GJB2相关耳聋进行微创基因筛查。

Minimally invasive genetic screen for GJB2 related deafness using dried blood spots.

作者信息

Nagy Attila L, Csáki Róbert, Klem József, Rovó László, Tóth Ferenc, Tálosi Gyula, Jóri József, Kovács Kornél, Kiss József Géza

机构信息

University of Szeged, Albert Szent-Györgyi Pharmaceutical and Medical Centre, Department of Oto-rhino-laryngology and Head and Neck Surgery, 6725, Tisza Lajos krt. 111, Szeged, Hungary.

出版信息

Int J Pediatr Otorhinolaryngol. 2010 Jan;74(1):75-81. doi: 10.1016/j.ijporl.2009.10.021. Epub 2009 Nov 24.

Abstract

OBJECTIVE

Nonsyndromic hearing loss is one of the most abundant human sensory disorders, and can be found in 1 out of 1000 newborns. In 60-70% of the cases this disorder is hereditary. The phenotype varies from moderate hearing loss to almost complete deafness, often only revealed in late childhood. Early detection of hearing related genetic variations in the first few weeks of life would allow planning of the audiological and logopedical procedures to maintain the children's normal audiological and speech development, and if required a cochlear implantation can be planned in time. We wanted to evaluate, whether the blood samples collected from neonates onto Guthrie cards (dried blood spots, or DBS), and blood collected from people of various ages into blood collecting tubes is equally usable for genetic testing. The quality of the samples on DBS's for genetic tests after an extended period of storage was evaluated. The methods for sample preparation and analysis were also evaluated.

METHODS

Two DNA extraction methods were compared on the samples. We extracted DNA from whole blood with the Versagene Blood Kit from Gentra, and from DBS's with boiling. Allele-specific PCRs (AS-PCR) were carried out on each sample. Samples were analyzed with AS-PCR and sequencing, for the 35delG mutation in the GJB2 (Cx26) gene. Freshly drawn and dried blood spot samples stored for several years were used in the experiments.

RESULTS

An AS-PCR method for detecting 35delG mutation on DNA extracted from Guthrie cards was validated. Blood samples up to 10 years of storage were applicable in the screen. 84 patients were found with 35delG mutations, both heterozygous (with no detected hearing related phenotypical discrepancies), and homozygous (phenotipically with moderate to severe hearing loss) forms.

CONCLUSIONS

The dried blood spots on Guthrie cards require only three drops of blood to be collected from children, which causes less stress than taking 3 ml of blood. The blood stored on Guthrie cards can be used to store DNA samples for at least 10 years. Even under suboptimal storage conditions the samples' DNA remains intact for genetic testing. Compared to blood collection tubes Guthrie cards cost less, are easier to transport and store.

摘要

目的

非综合征性听力损失是人类最常见的感觉障碍之一,每1000名新生儿中就有1例受其影响。在60%至70%的病例中,这种障碍是遗传性的。其表型从中度听力损失到几乎完全失聪不等,通常在儿童晚期才被发现。在生命的最初几周内早期检测与听力相关的基因变异,将有助于规划听力和言语治疗程序,以维持儿童正常的听力和言语发育,如有需要,还可及时安排人工耳蜗植入。我们想评估从新生儿采集到Guthrie卡片上的血样(干血斑,或DBS)以及从不同年龄段人群采集到采血管中的血液,是否同样适用于基因检测。评估了长期储存后用于基因检测的DBS样本的质量。还评估了样本制备和分析方法。

方法

对样本比较了两种DNA提取方法。我们使用Gentra公司的Versagene Blood Kit从全血中提取DNA,并用煮沸法从DBS中提取DNA。对每个样本进行等位基因特异性PCR(AS-PCR)。用AS-PCR和测序分析样本中GJB2(Cx26)基因的35delG突变。实验使用了新采集的和储存数年的干血斑样本。

结果

验证了一种用于检测从Guthrie卡片提取的DNA上35delG突变的AS-PCR方法。储存长达10年的血样适用于筛查。发现84例患者存在35delG突变,包括杂合子(未检测到与听力相关的表型差异)和纯合子(表型为中度至重度听力损失)形式。

结论

Guthrie卡片上的干血斑仅需从儿童采集三滴血,比采集3毫升血液造成的压力更小。储存在Guthrie卡片上的血液可用于储存DNA样本至少10年。即使在储存条件欠佳的情况下,样本的DNA仍保持完整,可用于基因检测。与采血管相比,Guthrie卡片成本更低,更易于运输和储存。

相似文献

1
Minimally invasive genetic screen for GJB2 related deafness using dried blood spots.
Int J Pediatr Otorhinolaryngol. 2010 Jan;74(1):75-81. doi: 10.1016/j.ijporl.2009.10.021. Epub 2009 Nov 24.
2
Connexin-26 gene analysis in hearing-impaired newborns.
Genet Test. 2000;4(4):345-9. doi: 10.1089/109065700750065072.
3
Newborn genetic screening for high risk deafness-associated mutations with a new Tetra-primer ARMS PCR kit.
Int J Pediatr Otorhinolaryngol. 2013 Sep;77(9):1440-5. doi: 10.1016/j.ijporl.2013.05.040. Epub 2013 Jun 29.
5
[A follow-up study of abnormal mutation in neonatal deafness gene screening].
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2019 Dec 7;54(12):881-887. doi: 10.3760/cma.j.issn.1673-0860.2019.12.001.
6
Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.
JAMA. 1999 Jun 16;281(23):2211-6. doi: 10.1001/jama.281.23.2211.
7
Comprehensive Genetic Testing for Deafness from Fresh and Archived Dried Blood Spots.
Otolaryngol Head Neck Surg. 2018 Dec;159(6):1058-1060. doi: 10.1177/0194599818797291. Epub 2018 Aug 28.
9
[The effects of newborn genetic screening for GJB2 and hearing follow-ups].
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2015 Feb;29(4):314-8.
10

引用本文的文献

1
The Comparison of PCR Kits for the Detection of Erythrocytic Parasites on Filter Paper.
J Trop Med. 2022 Aug 13;2022:5715436. doi: 10.1155/2022/5715436. eCollection 2022.
2
Maximizing deoxyribonucleic acid yield from dried blood spots.
J Diabetes Sci Technol. 2010 Mar 1;4(2):250-4. doi: 10.1177/193229681000400204.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验