Your browser doesn't support javascript.
loading
Reference interval establishment and correlation research of urine thromboxane metabolites: Unveiling new possibilities in platelet activation.
Cao, Yunfeng; Zhao, Furong; Wang, Shuang; Li, Ying; Li, Shuainan; Cui, Xueting.
Afiliação
  • Cao Y; Shanghai-MOST Key Laboratory of Health and Disease Genomics, NHC Key Lab of Reproduction Regulation, Shanghai institute for Biomedical and Pharmaceutical Technologies, Shanghai, China. Electronic address: caoyunfeng@sibpt.com.
  • Zhao F; Clinical research department, Dalian Boyuan Medical Technology Co., Ltd, Dalian, China; Liaoning Provincial Key Laboratory of Clinical Oncology Metabonomics, Jinzhou Medical University, Jinzhou, China.
  • Wang S; Clinical research department, Dalian Boyuan Medical Technology Co., Ltd, Dalian, China; Department of medical Research, Dalian Runsheng Kangtai Medical Lab Co. Ltd, Dalian, China.
  • Li Y; Clinical research department, Dalian Boyuan Medical Technology Co., Ltd, Dalian, China; Liaoning Provincial Key Laboratory of Clinical Oncology Metabonomics, Jinzhou Medical University, Jinzhou, China.
  • Li S; Clinical research department, Dalian Boyuan Medical Technology Co., Ltd, Dalian, China.
  • Cui X; Clinical research department, Dalian Boyuan Medical Technology Co., Ltd, Dalian, China; Department of medical Research, Dalian Runsheng Kangtai Medical Lab Co. Ltd, Dalian, China.
Clin Chim Acta ; 558: 119672, 2024 May 15.
Article em En | MEDLINE | ID: mdl-38621589
ABSTRACT

BACKGROUND:

Thromboxane metabolites could indirectly reflect platelet activation, among which 11-dehydro-thromboxane B2 (11dhTxB2) and 11-dehydro-2, 3-dinor thromboxane B2 (11dh23dinorTxB2) are two stable metabolites that are abundant in urine, and both are closely related to disease progression and drug use. However, most clinical application studies have focused on the single indicator of 11dhTxB2. We propose an LC-MS/MS method suitable for routine clinical screening with simultaneous determination of both metabolites and conduct preliminary studies in different populations. METHODS AND

RESULTS:

The thromboxane metabolites were extracted by liquid-liquid extraction and determined by LC-MS/MS. Reference intervals (RI) were established in 333 healthy adults and validated in 25 patients with coronary atherosclerosis (CA). This LC-MS/MS method was over a wide quantitative range (0.1-10 µmol/L), the imprecision and accuracy were 5.2 %-11 % and 89.3 %-106.5 %, and was suitable for clinical routine quantitative screening. The 95th percentile RI of unire 11dhTxB2 was 1220 (95 % CI 1048, 1376) pg mg Cr -1, for 11dh23dinorTxB2, RI was 908 (95 % CI 821, 1102) pg mg Cr -1. For the first time, we found a significant correlation between 11dhTxB2 and 11dh23dinorTxB2 in both healthy adults (r = 0.67, P < 0.001) and CA patients (r = 0.77, P < 0.001).

CONCLUSION:

The establishment of RI provides a reference for diseases related to platelet activation and the use of drugs, and the first discovery of the correlation between 11dhTxB2 and 11dh23dinorTxB2 in urine provides a new possibilitie for the diagnostic and prognostic of cardiovascular diseases.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tromboxano B2 / Ativação Plaquetária / Espectrometria de Massas em Tandem Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Chim Acta Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tromboxano B2 / Ativação Plaquetária / Espectrometria de Massas em Tandem Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Chim Acta Ano de publicação: 2024 Tipo de documento: Article