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Circulating biomarkers associated with aortic diameter in male and female patients with thoracic aortic disease: a cross-sectional study

OBJECTIVE: As thoracic aortic disease (TAD) is generally asymptomatic, biomarkers are needed to provide insight into early progression. We aimed to examine the association between circulating blood biomarkers and the maximal thoracic aortic diameter (TADmax). METHODS: In this cross-sectional study,...

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Autores principales: Meccanici, Frederike, Thijssen, Carlijn G E, Dekker, Silvy, Bons, Lidia R, Gökalp, Arjen L, de Rijke, Yolanda B, Takkenberg, Johanna J M, Mokhles, Mostafa M, Bekkers, Jos A, Boersma, Eric, Bouwens, Elke, van der Bosch, Annemien E, van Kimmenade, Roland R L, Roos-Hesselink, Jolien W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314683/
https://www.ncbi.nlm.nih.gov/pubmed/37385730
http://dx.doi.org/10.1136/openhrt-2023-002317
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author Meccanici, Frederike
Thijssen, Carlijn G E
Dekker, Silvy
Bons, Lidia R
Gökalp, Arjen L
de Rijke, Yolanda B
Takkenberg, Johanna J M
Mokhles, Mostafa M
Bekkers, Jos A
Boersma, Eric
Bouwens, Elke
van der Bosch, Annemien E
van Kimmenade, Roland R L
Roos-Hesselink, Jolien W
author_facet Meccanici, Frederike
Thijssen, Carlijn G E
Dekker, Silvy
Bons, Lidia R
Gökalp, Arjen L
de Rijke, Yolanda B
Takkenberg, Johanna J M
Mokhles, Mostafa M
Bekkers, Jos A
Boersma, Eric
Bouwens, Elke
van der Bosch, Annemien E
van Kimmenade, Roland R L
Roos-Hesselink, Jolien W
author_sort Meccanici, Frederike
collection PubMed
description OBJECTIVE: As thoracic aortic disease (TAD) is generally asymptomatic, biomarkers are needed to provide insight into early progression. We aimed to examine the association between circulating blood biomarkers and the maximal thoracic aortic diameter (TADmax). METHODS: In this cross-sectional study, consecutive adult patients with a thoracic aortic diameter ≥40 mm and/or genetically proven hereditary TAD (HTAD) visiting our specialised outpatient clinic between 2017 and 2020 were prospectively included. Venous blood sampling and CT angiography and/or transthoracic echocardiography of the aorta were performed. Linear regression analyses were performed and estimates were presented as mean difference in TADmax in mm per doubling of standardised biomarker level. RESULTS: In total, 158 patients were included (median age 61 (50.3–68.8) years, 37.3% female). HTAD diagnosis was confirmed in 36 of 158 (22.7%) patients. TADmax was 43.9±5.2 mm in men vs 41.9±5.1 in women (p=0.030). In unadjusted analysis, significant associations with TADmax were found for interleukin-6 (1.15 (95% CI 0.33 to 1.96), p=0.006), growth differentiation factor-15 (1.01 (95% CI 0.18 to 1.84), p=0.018), microfibrillar-associated protein 4 (MFAP4) (−0.88 (95% CI −1.71 to 0.05), p=0.039) and triiodothyronine (T3) (−2.00 (95%CI −3.01 to 0.99), p<0.001). The association of MFAP4 with TADmax was stronger in women (p for interaction=0.020) and for homocysteine, an inverse association with TADmax was observed when compared with men (p for interaction=0.008). When adjusted for age, sex, hyperlipidaemia and HTAD, total cholesterol (1.10 (95% CI 0.27 to 1.93), p=0.010) and T3 (−1.20 (95% CI −2.14 to 0.25), p=0.014) were significantly associated with TADmax. CONCLUSIONS: Circulating biomarkers indicative of inflammation, lipid metabolism and thyroid function might be associated with TAD severity. Possible distinct biomarker patterns for men and women warrant further investigation.
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spelling pubmed-103146832023-07-02 Circulating biomarkers associated with aortic diameter in male and female patients with thoracic aortic disease: a cross-sectional study Meccanici, Frederike Thijssen, Carlijn G E Dekker, Silvy Bons, Lidia R Gökalp, Arjen L de Rijke, Yolanda B Takkenberg, Johanna J M Mokhles, Mostafa M Bekkers, Jos A Boersma, Eric Bouwens, Elke van der Bosch, Annemien E van Kimmenade, Roland R L Roos-Hesselink, Jolien W Open Heart Aortic and Vascular Disease OBJECTIVE: As thoracic aortic disease (TAD) is generally asymptomatic, biomarkers are needed to provide insight into early progression. We aimed to examine the association between circulating blood biomarkers and the maximal thoracic aortic diameter (TADmax). METHODS: In this cross-sectional study, consecutive adult patients with a thoracic aortic diameter ≥40 mm and/or genetically proven hereditary TAD (HTAD) visiting our specialised outpatient clinic between 2017 and 2020 were prospectively included. Venous blood sampling and CT angiography and/or transthoracic echocardiography of the aorta were performed. Linear regression analyses were performed and estimates were presented as mean difference in TADmax in mm per doubling of standardised biomarker level. RESULTS: In total, 158 patients were included (median age 61 (50.3–68.8) years, 37.3% female). HTAD diagnosis was confirmed in 36 of 158 (22.7%) patients. TADmax was 43.9±5.2 mm in men vs 41.9±5.1 in women (p=0.030). In unadjusted analysis, significant associations with TADmax were found for interleukin-6 (1.15 (95% CI 0.33 to 1.96), p=0.006), growth differentiation factor-15 (1.01 (95% CI 0.18 to 1.84), p=0.018), microfibrillar-associated protein 4 (MFAP4) (−0.88 (95% CI −1.71 to 0.05), p=0.039) and triiodothyronine (T3) (−2.00 (95%CI −3.01 to 0.99), p<0.001). The association of MFAP4 with TADmax was stronger in women (p for interaction=0.020) and for homocysteine, an inverse association with TADmax was observed when compared with men (p for interaction=0.008). When adjusted for age, sex, hyperlipidaemia and HTAD, total cholesterol (1.10 (95% CI 0.27 to 1.93), p=0.010) and T3 (−1.20 (95% CI −2.14 to 0.25), p=0.014) were significantly associated with TADmax. CONCLUSIONS: Circulating biomarkers indicative of inflammation, lipid metabolism and thyroid function might be associated with TAD severity. Possible distinct biomarker patterns for men and women warrant further investigation. BMJ Publishing Group 2023-06-29 /pmc/articles/PMC10314683/ /pubmed/37385730 http://dx.doi.org/10.1136/openhrt-2023-002317 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Aortic and Vascular Disease
Meccanici, Frederike
Thijssen, Carlijn G E
Dekker, Silvy
Bons, Lidia R
Gökalp, Arjen L
de Rijke, Yolanda B
Takkenberg, Johanna J M
Mokhles, Mostafa M
Bekkers, Jos A
Boersma, Eric
Bouwens, Elke
van der Bosch, Annemien E
van Kimmenade, Roland R L
Roos-Hesselink, Jolien W
Circulating biomarkers associated with aortic diameter in male and female patients with thoracic aortic disease: a cross-sectional study
title Circulating biomarkers associated with aortic diameter in male and female patients with thoracic aortic disease: a cross-sectional study
title_full Circulating biomarkers associated with aortic diameter in male and female patients with thoracic aortic disease: a cross-sectional study
title_fullStr Circulating biomarkers associated with aortic diameter in male and female patients with thoracic aortic disease: a cross-sectional study
title_full_unstemmed Circulating biomarkers associated with aortic diameter in male and female patients with thoracic aortic disease: a cross-sectional study
title_short Circulating biomarkers associated with aortic diameter in male and female patients with thoracic aortic disease: a cross-sectional study
title_sort circulating biomarkers associated with aortic diameter in male and female patients with thoracic aortic disease: a cross-sectional study
topic Aortic and Vascular Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314683/
https://www.ncbi.nlm.nih.gov/pubmed/37385730
http://dx.doi.org/10.1136/openhrt-2023-002317
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