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血清表面活性剂蛋白 D 和 SFTPD 基因变异与丹麦儿童、青少年和青年期哮喘的相关性研究。

Association of serum surfactant protein D and SFTPD gene variants with asthma in Danish children, adolescents, and young adults.

机构信息

Hans Christian Andersen Children's Hospital, Odense University Hospital, Odense, Denmark.

Open Patient Data Explorative Network, Odense University Hospital, Odense, Denmark.

出版信息

Immun Inflamm Dis. 2022 Feb;10(2):189-200. doi: 10.1002/iid3.560. Epub 2021 Nov 15.

Abstract

BACKGROUND

Surfactant Protein D (SP-D) is a pattern recognition molecule belonging to the family of collectins expressed in multiple human organ systems, including the lungs. Previous studies have shown that SP-D levels in bronchoalveolar lavage samples decrease and serum levels increase in patients suffering from asthma, possibly due to a combination of induced SP-D synthesis and decreased air-blood barrier integrity. The aims of this study were to investigate whether serum levels of SP-D and common variants in the SP-D gene were associated with asthma in adolescents and young adults.

METHODS

Prospective observational study including 449 adolescents and young adults (age 11-27 years) previously diagnosed with asthma during a 2-year period from 2003 to 2005 (0-16 years). At follow-up from 2016 to 2017, 314 healthy controls with no history of asthma were recruited. Serum SP-D was analyzed on samples obtained at baseline as well as samples obtained at follow-up. SP-D genotyping was performed for rs721917, rs2243639, and rs3088308.

RESULTS

No differences were found in mean levels of sSP-D and SFTPD genotype among subjects with current asthma, no current asthma, and controls. Serum SP-D and SFTPD genotype were not associated with any clinical parameters of asthma. Furthermore, baseline sSP-D was not associated with asthma at follow-up.

CONCLUSION

Serum surfactant protein D and common SP-D gene variants were not associated with asthma in Danish adolescents and young adults with mild to moderate asthma. Serum surfactant protein D did not demonstrate any value as a clinical biomarker of asthma.

摘要

背景

表面活性蛋白 D(SP-D)是一种模式识别分子,属于凝集素家族,在包括肺部在内的多个人体器官系统中表达。先前的研究表明,患有哮喘的患者支气管肺泡灌洗液样本中的 SP-D 水平降低,血清水平升高,这可能是由于诱导的 SP-D 合成和空气-血屏障完整性降低的综合作用。本研究旨在探讨血清 SP-D 水平和 SP-D 基因常见变异是否与青少年和年轻成年人的哮喘有关。

方法

前瞻性观察研究纳入了 449 名青少年和年轻成年人(年龄 11-27 岁),他们在 2003 年至 2005 年的 2 年期间被诊断为哮喘(0-16 岁)。在 2016 年至 2017 年的随访中,招募了 314 名没有哮喘病史的健康对照者。在基线和随访时采集血清样本,分析 SP-D 水平。对 rs721917、rs2243639 和 rs3088308 进行 SP-D 基因分型。

结果

在当前哮喘、无当前哮喘和对照组中,sSP-D 的平均水平和 SFTPD 基因型没有差异。血清 SP-D 和 SFTPD 基因型与哮喘的任何临床参数均无关。此外,基线 sSP-D 与随访时的哮喘无关。

结论

在丹麦患有轻度至中度哮喘的青少年和年轻成年人中,血清表面活性蛋白 D 和常见的 SP-D 基因变异与哮喘无关。血清表面活性蛋白 D 作为哮喘的临床生物标志物没有任何价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0460/8767520/412050c76ae8/IID3-10-189-g001.jpg

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