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Published on: August 28, 2018
Association between Achilles tendon xanthoma and severity of coronary artery disease in patients undergoing
Hideki Kitahara1, Takashi Nakayama1, Yoshihide Fujimoto1
1Department of Cardiovascular Medicine, Chiba University Graduate School of Medicine, Chiba, Japan.
Insights
Achilles tendon xanthoma (ATX) is linked to more severe coronary artery disease (CAD) in patients undergoing percutaneous coronary intervention. Detecting ATX can help identify individuals with advanced CAD, beyond its role in diagnosing familial hypercholesterolemia.
Area of Science:
- Cardiology
- Genetics
- Radiology
Background:
- Achilles tendon xanthoma (ATX) is a key diagnostic sign for familial hypercholesterolemia (FH).
- Some patients with ATX do not meet FH diagnostic criteria, suggesting other clinical implications.
- The association between ATX and coronary artery disease (CAD) severity requires further investigation.
Purpose of the Study:
- To evaluate the relationship between ATX and the severity of CAD in patients undergoing percutaneous coronary intervention (PCI).
- To determine if ATX is an independent predictor of advanced CAD.
Main Methods:
- 394 patients with CAD undergoing PCI were analyzed.
- Achilles tendon thickness was measured using soft X-ray radiography; ATX was defined as ≥9 mm thickness.
- CAD severity was quantified using the SYNTAX score.
Main Results:
- 43 patients (10.9%) had ATX; 16 (4.1%) were diagnosed with FH.
- The ATX group exhibited higher BMI, lower HDL cholesterol, and increased prevalence of FH, diabetes, and prior cardiovascular events.
- Patients with ATX had significantly higher SYNTAX scores and a greater likelihood of severe CAD (SYNTAX score ≥23) compared to those without ATX.
- A progressive increase in SYNTAX score and severe CAD prevalence was observed with increasing Achilles tendon thickness.
- Male sex, diabetes, and ATX were identified as independent predictors of higher SYNTAX scores.
Conclusions:
- ATX is independently associated with increased CAD severity in patients undergoing PCI.
- Identifying ATX can aid in diagnosing FH and, importantly, in detecting patients with advanced coronary artery disease.
Background:
Tendon xanthoma, represented as Achilles tendon xanthoma (ATX), is one of the important diagnostic criteria for familial hypercholesterolemia (FH). However, there are some cases with ATX who do not meet these criteria. This study aimed to investigate the severity of coronary artery disease (CAD) in patients with ATX.
Methods:
A total of 394 patients with CAD undergoing percutaneous coronary intervention (PCI) at Chiba University Hospital between June 2016 and February 2018 were enrolled. Soft X-ray radiography of Achilles tendon was performed, and a maximum thickness of 9 mm or more was regarded as ATX. Heterozygous FH was diagnosed according to the diagnostic criteria proposed by the Japan Atherosclerosis Society in 2017. CAD severity was assessed by SYNTAX score before the first PCI during the study period.
Results:
There were 43 (10.9%) patients with ATX, and 16 (4.1%) were diagnosed as FH (15 with ATX and 1 without ATX). The ATX group showed greater body mass index, lower high-density lipoprotein cholesterol level, and the higher prevalence of FH, diabetes, prior myocardial infarction, acute coronary syndrome, multivessel disease, hemodialysis, and prior statin administration. SYNTAX score and the rate of SYNTAX score ≥23 were significantly higher in the ATX group compared with the non-ATX group (p < 0.001 for each). When patients were divided into quartiles according to Achilles tendon thickness, SYNTAX score and the prevalence of SYNTAX score ≥23 were progressively increased in favor of greater Achilles tendon thickness (p < 0.001 for each). Multivariate analysis determined male, diabetes, and ATX as independent predictors for higher SYNTAX score.
Conclusions:
In CAD patients undergoing PCI, ATX was independently associated with severity of CAD. Detecting ATX may be useful not only for diagnosing FH, but also for identifying patients with advanced CAD.
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