Association of serum vitamin D with diagnosis and growth of abdominal aortic aneurysm

Objective: We examined the associations between 25-hydroxy vitamin D (25(OH)D3) concentration and the diagnosis and growth of abdominal aortic aneurysm (AAA). Methods: AAA cases and healthy controls were recruited from vascular centers or the community. A subset of participants with AAA were monitor...

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Published in:JVS - Vascular Science
Main Authors: Shivshankar Thanigaimani, PhD, Rachel E. Neale, PhD, Mary Waterhouse, PhD, Joseph V. Moxon, PhD, Bu B. Yeap, PhD, Paul E. Norman, PhD, Leon Flicker, PhD, Graeme J. Hankey, PhD, Jason Jenkins, PhD, Frank Quigley, PhD, Michael W. Clarke, PhD, Jonathan Golledge, MA, FRCS, FRACS
Format: Article
Language:English
Published: Elsevier 2024-01-01
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Online Access:http://www.sciencedirect.com/science/article/pii/S2666350324000191
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author Shivshankar Thanigaimani, PhD
Rachel E. Neale, PhD
Mary Waterhouse, PhD
Joseph V. Moxon, PhD
Bu B. Yeap, PhD
Paul E. Norman, PhD
Leon Flicker, PhD
Graeme J. Hankey, PhD
Jason Jenkins, PhD
Frank Quigley, PhD
Michael W. Clarke, PhD
Jonathan Golledge, MA, FRCS, FRACS
author_facet Shivshankar Thanigaimani, PhD
Rachel E. Neale, PhD
Mary Waterhouse, PhD
Joseph V. Moxon, PhD
Bu B. Yeap, PhD
Paul E. Norman, PhD
Leon Flicker, PhD
Graeme J. Hankey, PhD
Jason Jenkins, PhD
Frank Quigley, PhD
Michael W. Clarke, PhD
Jonathan Golledge, MA, FRCS, FRACS
author_sort Shivshankar Thanigaimani, PhD
collection DOAJ
container_title JVS - Vascular Science
description Objective: We examined the associations between 25-hydroxy vitamin D (25(OH)D3) concentration and the diagnosis and growth of abdominal aortic aneurysm (AAA). Methods: AAA cases and healthy controls were recruited from vascular centers or the community. A subset of participants with AAA were monitored by repeat ultrasound examination to assess AAA growth. Serum 25(OH)D3 concentration was measured using a validated mass spectrometry method and categorized into guideline-recommended cut-points after deseasonalization. The associations between deseasonalized 25(OH)D3 concentration and AAA diagnosis and growth were examined using logistic regression and linear mixed effects modeling. Results: A total of 4673 participants consisting of 873 (455 controls and 418 cases) from Queensland and 3800 (3588 controls and 212 cases) from Western Australia were recruited. For every 1 standard deviation increase in 25(OH)D3 concentration, odds of AAA diagnosis was significantly reduced in both Queensland (adjusted odds ratio: 0.81; 95% confidence interval [CI]: 0.69-0.95; P = .009) and Western Australia (adjusted odds ratio: 0.80; 95% CI: 0.68-0.94; P = .005) cohorts. A subset of 310 eligible participants with small AAA from both regions were followed for a median of 4.2 (interquartile range: 2.0-5.8) years. Compared with vitamin D sufficient participants (50 to ˂75 nmol/L), annual mean AAA growth was significantly greater in those with higher vitamin D (≥75 nmol/L) (adjusted mean difference: 0.1 mm/y, 95% CI: 0.1-0.2; P < .001). Conclusions: High 25(OH)D3 concentration was paradoxically associated with a lower likelihood of AAA diagnosis and faster AAA growth. Further research is needed to resolve these conflicting findings. : Clinical Relevance: The findings of this study suggest that relative vitamin D deficiency increases the risk of abdominal aortic aneurysm diagnosis, but paradoxically high circulating markers of vitamin D are associated with faster aneurysm growth. These findings support the need for vitamin D sufficiency not excess, but need validation in other cohorts before incorporation into clinical management protocols.
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spelling doaj-art-5a9e8cf95fba4e2f976c6d5284e1176d2025-08-20T02:35:29ZengElsevierJVS - Vascular Science2666-35032024-01-01510020810.1016/j.jvssci.2024.100208Association of serum vitamin D with diagnosis and growth of abdominal aortic aneurysmShivshankar Thanigaimani, PhD0Rachel E. Neale, PhD1Mary Waterhouse, PhD2Joseph V. Moxon, PhD3Bu B. Yeap, PhD4Paul E. Norman, PhD5Leon Flicker, PhD6Graeme J. Hankey, PhD7Jason Jenkins, PhD8Frank Quigley, PhD9Michael W. Clarke, PhD10Jonathan Golledge, MA, FRCS, FRACS11Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, QLD, Australia; Australian Institute of Tropical Health and Medicine, James Cook University, Townsville, QLD, AustraliaPopulation Health Department, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia; School of Public Health, University of Queensland, Brisbane, QLD, AustraliaPopulation Health Department, QIMR Berghofer Medical Research Institute, Brisbane, QLD, AustraliaQueensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, QLD, Australia; Australian Institute of Tropical Health and Medicine, James Cook University, Townsville, QLD, AustraliaMedical School, University of Western Australia, Perth, WA, Australia; Department of Endocrinology and Diabetes, Fiona Stanley Hospital, Perth, WA, AustraliaMedical School, University of Western Australia, Perth, WA, AustraliaMedical School, University of Western Australia, Perth, WA, AustraliaMedical School, University of Western Australia, Perth, WA, Australia; Perron Institute for Neurological and Translational Science, Perth, WA, AustraliaDepartment of Vascular Surgery, Royal Brisbane and Women's Hospital, Brisbane, QLD, AustraliaMater Hospital, Townsville, QLD, AustraliaMetabolomics Australia, Centre for Microscopy, Characterisation and Analysis, The University of Western Australia, Perth, WA, Australia; School of Biomedical Sciences, Faculty of Health and Medical Sciences, The University of Western Australia, Perth, WA, AustraliaQueensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, QLD, Australia; Australian Institute of Tropical Health and Medicine, James Cook University, Townsville, QLD, Australia; Department of Vascular and Endovascular Surgery, Townsville University Hospital, Townsville, QLD, Australia; Correspondence: Jonathan Golledge, MA, FRCS, FRACS, Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, 1 James Cook Dr, Douglas, QLD 4814, AustraliaObjective: We examined the associations between 25-hydroxy vitamin D (25(OH)D3) concentration and the diagnosis and growth of abdominal aortic aneurysm (AAA). Methods: AAA cases and healthy controls were recruited from vascular centers or the community. A subset of participants with AAA were monitored by repeat ultrasound examination to assess AAA growth. Serum 25(OH)D3 concentration was measured using a validated mass spectrometry method and categorized into guideline-recommended cut-points after deseasonalization. The associations between deseasonalized 25(OH)D3 concentration and AAA diagnosis and growth were examined using logistic regression and linear mixed effects modeling. Results: A total of 4673 participants consisting of 873 (455 controls and 418 cases) from Queensland and 3800 (3588 controls and 212 cases) from Western Australia were recruited. For every 1 standard deviation increase in 25(OH)D3 concentration, odds of AAA diagnosis was significantly reduced in both Queensland (adjusted odds ratio: 0.81; 95% confidence interval [CI]: 0.69-0.95; P = .009) and Western Australia (adjusted odds ratio: 0.80; 95% CI: 0.68-0.94; P = .005) cohorts. A subset of 310 eligible participants with small AAA from both regions were followed for a median of 4.2 (interquartile range: 2.0-5.8) years. Compared with vitamin D sufficient participants (50 to ˂75 nmol/L), annual mean AAA growth was significantly greater in those with higher vitamin D (≥75 nmol/L) (adjusted mean difference: 0.1 mm/y, 95% CI: 0.1-0.2; P < .001). Conclusions: High 25(OH)D3 concentration was paradoxically associated with a lower likelihood of AAA diagnosis and faster AAA growth. Further research is needed to resolve these conflicting findings. : Clinical Relevance: The findings of this study suggest that relative vitamin D deficiency increases the risk of abdominal aortic aneurysm diagnosis, but paradoxically high circulating markers of vitamin D are associated with faster aneurysm growth. These findings support the need for vitamin D sufficiency not excess, but need validation in other cohorts before incorporation into clinical management protocols.http://www.sciencedirect.com/science/article/pii/S2666350324000191Vitamin DAbdominal aortic aneurysmAAA diagnosisAAA growth
spellingShingle Shivshankar Thanigaimani, PhD
Rachel E. Neale, PhD
Mary Waterhouse, PhD
Joseph V. Moxon, PhD
Bu B. Yeap, PhD
Paul E. Norman, PhD
Leon Flicker, PhD
Graeme J. Hankey, PhD
Jason Jenkins, PhD
Frank Quigley, PhD
Michael W. Clarke, PhD
Jonathan Golledge, MA, FRCS, FRACS
Association of serum vitamin D with diagnosis and growth of abdominal aortic aneurysm
Vitamin D
Abdominal aortic aneurysm
AAA diagnosis
AAA growth
title Association of serum vitamin D with diagnosis and growth of abdominal aortic aneurysm
title_full Association of serum vitamin D with diagnosis and growth of abdominal aortic aneurysm
title_fullStr Association of serum vitamin D with diagnosis and growth of abdominal aortic aneurysm
title_full_unstemmed Association of serum vitamin D with diagnosis and growth of abdominal aortic aneurysm
title_short Association of serum vitamin D with diagnosis and growth of abdominal aortic aneurysm
title_sort association of serum vitamin d with diagnosis and growth of abdominal aortic aneurysm
topic Vitamin D
Abdominal aortic aneurysm
AAA diagnosis
AAA growth
url http://www.sciencedirect.com/science/article/pii/S2666350324000191
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