Preanalytical Pitfalls in Untargeted Plasma Nuclear Magnetic Resonance Metabolomics of Endocrine Hypertension

Author:

Bliziotis Nikolaos G.,Kluijtmans Leo A. J.ORCID,Tinnevelt Gerjen H.ORCID,Reel ParminderORCID,Reel Smarti,Langton Katharina,Robledo MercedesORCID,Pamporaki Christina,Pecori AlessioORCID,Van Kralingen Josie,Tetti Martina,Engelke Udo F. H.,Erlic ZoranORCID,Engel Jasper,Deutschbein Timo,Nölting Svenja,Prejbisz Aleksander,Richter SusanORCID,Adamski JerzyORCID,Januszewicz Andrzej,Ceccato FilippoORCID,Scaroni Carla,Dennedy Michael C.,Williams Tracy A.,Lenzini Livia,Gimenez-Roqueplo Anne-PauleORCID,Davies Eleanor,Fassnacht MartinORCID,Remde HannaORCID,Eisenhofer Graeme,Beuschlein FelixORCID,Kroiss MatthiasORCID,Jefferson EmilyORCID,Zennaro Maria-Christina,Wevers Ron A.ORCID,Jansen Jeroen J.,Deinum JaapORCID,Timmers Henri J. L. M.

Abstract

Despite considerable morbidity and mortality, numerous cases of endocrine hypertension (EHT) forms, including primary aldosteronism (PA), pheochromocytoma and functional paraganglioma (PPGL), and Cushing’s syndrome (CS), remain undetected. We aimed to establish signatures for the different forms of EHT, investigate potentially confounding effects and establish unbiased disease biomarkers. Plasma samples were obtained from 13 biobanks across seven countries and analyzed using untargeted NMR metabolomics. We compared unstratified samples of 106 PHT patients to 231 EHT patients, including 104 PA, 94 PPGL and 33 CS patients. Spectra were subjected to a multivariate statistical comparison of PHT to EHT forms and the associated signatures were obtained. Three approaches were applied to investigate and correct confounding effects. Though we found signatures that could separate PHT from EHT forms, there were also key similarities with the signatures of sample center of origin and sample age. The study design restricted the applicability of the corrections employed. With the samples that were available, no biomarkers for PHT vs. EHT could be identified. The complexity of the confounding effects, evidenced by their robustness to correction approaches, highlighted the need for a consensus on how to deal with variabilities probably attributed to preanalytical factors in retrospective, multicenter metabolomics studies.

Funder

European Union

Publisher

MDPI AG

Subject

Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference84 articles.

1. Raised Blood Pressure (SBP>=140 OR DBP>=90) (Crude Estimate);World Health Organization,2017

2. GBD 2017 Risk Factor Collaborators, Global, regional, and national age-sex-specific mortality for 282 causes of death in 195 countries and territories, 1980–2017: A systematic analysis for the Global Burden of Disease Study 2017;Lancet,2018

3. Observational Study Mortality in Treated Primary Aldosteronism

4. Cardiovascular events and target organ damage in primary aldosteronism compared with essential hypertension: a systematic review and meta-analysis

5. Is the Excess Cardiovascular Morbidity in Pheochromocytoma Related to Blood Pressure or to Catecholamines?

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3