Cited by 65Amyloidosis: Diagnosis, Treatment, OutcomesCardiovascular Health and Disease PreventionCardiac tumors and thrombi

Vascular abnormalities in primary amyloidosis

Modesto, K. M., Dispenzieri, A., Gertz, M., Cauduro, S. A., Khandheria, B. K., Seward, J. B., Kyle, R., Wood, C. M. +5 more·2007·European Heart Journal

Abstract

AIMS: Primary amyloidosis (AL) is a systemic disease; however, there is limited information regarding the presence and character of vascular abnormalities. METHODS AND RESULTS: Validated ultrasound techniques were used to prospectively determine carotid artery intimal-medial thickness (IMT) and brachial artery flow-mediated dilatation (FMD) in 59 consecutive AL patients and 17 age-similar, healthy, asymptomatic volunteers (CON). Carotid IMT was increased in AL when compared with CON (0.07 +/- 0.02 vs. 0.04 +/- 0.01 mm, P < 0.01). Similarly, brachial artery FMD was significantly lower in AL when compared with CON subjects (3 +/- 7 vs. 12 +/- 8%, P < 0.01). Multivariable analysis revealed that AL was associated with larger IMT and lower FMD after controlling for several confounding variables. However, within AL cases, there was not a significant association of cardiac vs. non-cardiac involvement with IMT or FMD (P = 0.1 and 0.2, respectively). CONCLUSION: AL is associated with abnormal vascular morphology and endothelial dysfunction. Vascular abnormalities do not appear to be related to echocardiographic evidence of cardiac involvement.

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  • Data on the risk of atherosclerosis in individuals with HDL-C-lowering mutations are contradictory.

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References 32 · Cited by 65

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  1. Celermajer DS, Sorensen KE, Gooch VM, Spiegelhalter DJ, Miller OI, Sullivan ID, Lloyd JK, Deanfield JE. Non-invasive detection of endothelial dysfunction in children and adults at risk of atherosclerosis. Lancet 1992; 340:1111-1115.

Authors
Modesto, K. M., Dispenzieri, A., Gertz, M., Cauduro, S. A., Khandheria, B. K., Seward, J. B., Kyle, R., Wood, C. M., Bailey, K. R., Tajik, A. J., Miller, F. A., Pellikka, P. A., & Abraham, T. P.
Affiliations
Mayo Clinic (US)
Corresponding author
Abraham, T. P.
Venue
European Heart Journal
Published
2007-04-02
Volume
28
Issue
8
Pages
1019-1024
ISSN
  • 0195-668X (ISSN-L)
  • 1522-9645
OpenAlex
W2134368433
Cited by
65
References
32
Citations by year
2026: 2 · 2025: 5 · 2024: 6 · 2023: 5 · 2022: 9 · 2021: 6 · 2020: 3 · 2019: 6 · 2018: 1 · 2017: 6 · 2016: 4 · 2015: 1 · 2014: 2 · 2013: 2 · 2012: 2
FWCI
0.40
Type
journal article
Language
en
Open access
closed
Locations
  • European Heart Journal (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health
  • National Heart, Lung, and Blood Institute (HL076513-02, R21HL076513)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Amyloidosis: Diagnosis, Treatment, Outcomes
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Health and Disease Prevention
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac tumors and thrombi
Keywords
AL amyloidosis, vascular anomalies, carotid intima-media thickness, flow-mediated dilation, endothelial dysfunction, brachial artery, cardiac involvement, amyloidosis
MeSH terms
Aged, Amyloidosis, Brachial Artery, Carotid Arteries, Dilatation, Pathologic, Endothelium, Vascular, Female, Humans, Male, Prospective Studies, Ultrasonography, Vascular Diseases, Tunica Intima

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