Next Article in Journal
Is Conduction System Pacing a Valuable Alternative to Biventricular Pacing for Cardiac Resynchronization Therapy?
Previous Article in Journal
Serum Biomarkers and Their Association with Myocardial Function and Exercise Capacity in Cardiac Transthyretin Amyloidosis
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
JCDD
Volume 11
Issue 5
10.3390/jcdd11050143
jcdd-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Association between Abdominal Aortic Calcification and Coronary Heart Disease in Essential Hypertension: A Cross-Sectional Study from the 2013–2014 National Health and Nutrition Examination Survey

by
Lan He
1,†,
Xu Li
1,†,
E Shen
2,* and
Yong-Ming He
1,*
1
Division of Cardiology, The First Affiliated Hospital of Soochow University, 188 Shizi Ave., Gusu District, Suzhou 215006, China
2
Department of Ultrasound, Shanghai Chest Hospital, School of Medicine, Shanghai Jiao Tong University, 241 Huaihai West Road, Xuhui District, Shanghai 200030, China
*
Authors to whom correspondence should be addressed.
†
These authors contributed equally to this work.
J. Cardiovasc. Dev. Dis. 2024, 11(5), 143; https://doi.org/10.3390/jcdd11050143
Submission received: 24 March 2024 / Revised: 26 April 2024 / Accepted: 29 April 2024 / Published: 2 May 2024
Browse Figures
Versions Notes

Abstract

:
Background: This study aimed to investigate the association between abdominal aortic calcification (AAC) and coronary heart disease (CHD) in essential hypertension (EH). Methods: This study included patients diagnosed with EH during the 2013–2014 NHANES survey cycle. The study cohort was categorized into the following four groups based on their AAC-24 score: no AAC (0); mild AAC (1–4); moderate AAC (5–15); and severe AAC (16–24). Logistic regression models were used to assess the association between AAC and CHD. Restricted cubic spline curves (RCS) were used to explore possible nonlinear relationships between AAC and CHD. Results: The prevalence of CHD was found to be higher in the moderate AAC and severe AAC groups than in the group without AAC (40.1% versus 30.9%, 47.7% versus 30.9%). On a continuous scale, the fully adjusted model showed a 7% increase in the risk of CHD prevalence per score increase in AAC [OR (95% CI) = 1.07 (1.03–1.11)]. On a categorical scale, the fully adjusted model showed the risk of CHD prevalence in EH patients with moderate AAC and severe AAC was 2.06 (95%CI, 1.23–3.45) and 2.18 (1.09–5.25) times higher than that in patients without AAC, respectively. The RCS curve suggested a dose-response linear relationship between AAC and CHD. Conclusion: These findings highlight that in patients with EH, a higher severity of AAC is associated with a higher risk of CHD prevalence.

1. Introduction

Arterial calcification, a primary indicator of arterial stiffness, is strongly correlated with cardiovascular disease risk [1]. It has been unequivocally identified as a predictor for coronary heart disease (CHD) [2,3]. Commonly-used clinical measures of arterial calcification include coronary artery calcification (CAC) and abdominal aortic calcification (AAC) [4]. AAC is increasingly recognized due to its easier localization and quantification, as well as its earlier occurrence compared to CAC [5,6]. Serving as a sensitive predictor of CHD, AAC has been shown to outperform the Framingham risk score [7]. In a 5-year prospective study, patients with AAC scores above 5.5 exhibited a significantly higher incidence of CHD compared to those with AAC scores below 5.5 [8]. Jurgens et al. found that blacks tended to have higher AAC scores than whites, particularly among black women, which may help explain their disparate rates of CHD (3.6% for black women vs. 1.6% for white women) [9].
Hypertension represents a significant subgroup vulnerable to CHD [10,11]. Research indicates that approximately 71.8% of CHD patients also have comorbid hypertension, while about 30% of hypertensive patients attending outpatient clinics are concurrently diagnosed with CHD [12]. Moreover, the mortality rate from CHD is 2.3 times higher in the presence of hypertension [13]. Additionally, studies have revealed that hypertensive patients constitute the primary demographic affected by arterial calcification [14]. This susceptibility arises from the pathological changes characteristic of hypertension [15,16,17]. However, to our knowledge, the relationship between AAC and CHD in hypertensive patients has not been previously explored. Therefore, the objective of this study was to examine the association between AAC and CHD in essential hypertension (EH) using the cross-sectional design.

2. Methods

2.1. NHANES

NHANES, the National Health and Nutrition Examination Survey, is a cross-sectional, population-based survey designed to collect information about the health and nutrition status of the U.S. household population. The program surveys a nationally representative sample of approximately 5000 individuals each year, located in counties across the country, to represent the U.S. population. NHANES includes both an interview, which includes questions on demographics, socioeconomics, diet, and health, and a physical examination, which includes physiologic measurements, laboratory tests, and other components. The National Institutes of Health Research Ethics Review Board approved the NHANES survey protocol, and all participants signed and provided informed consent. NHANES data are publicly available from the official website [18].

2.2. Study Population

This study included patients diagnosed with EH during the 2013–2014 NHANES survey cycle. EH was defined as SBP ≥ 140 and/or DBP ≥ 90 mmHg or as a self-reported one by asking the question, “Has a doctor or other health professional ever told you that you have hypertension?” The exclusion criteria were as follows: (i) age < 18; (ii) without EH or missing data on EH; and (iii) missing data on AAC or CHD. The degree and extent of AAC were assessed using the AAC-24 semi-quantitative technique (Kauppila, 1997; Schousboe, 2007) [19,20]. The AAC score was extracted from the examination data for NHANES. Lateral spine images were acquired by dual-energy X-ray absorptiometry. Lateral spine images were analyzed in the region of L1–L4 vertebrae, which were divided into 4 segments with the midpoint of the intervertebral space as the boundary. The total calcification score of the anterior and posterior walls of the corresponding vessels was calculated for each spinal segment. The study population was divided into the following 4 groups according to the AAC-24 score: without AAC (0); mild AAC (1–4); moderate AAC (5–15); and severe AAC (16–24).

2.3. Study Outcome

The outcome of this study was CHD prevalence, which was self-reported by asking the question, “Have you been told by a doctor that you have CHD?”. CHD included all chronic coronary artery disease (stable angina, ischemic cardiomyopathy, and occult coronary artery disease) and acute coronary syndromes (unstable angina, non-ST-segment elevation myocardial infarction, and ST-segment elevation myocardial infarction).

2.4. Covariates

Age, sex, ethnicity, diabetes mellitus (DM), smoking, and drinking were obtained through questionnaires. The diagnosis of diabetes mellitus (DM) referred to the most recent ADA criteria (FPG ≥ 7.0 mmol/L, A1C ≥ 6.5%, 2-h OGTT ≥ 11.1 mmol/L, or a random plasma glucose ≥ 11.1 mmol/L) [21]. The definitions of smoking and drinking refer to the latest standards on the New Zealand Ministry of Health website [22]. Body mass index (BMI) and pulse were obtained by physical examination, where BMI was evaluated by body mass (kilograms) and body height (m2). Red blood cells (RBCs), white blood cells (WBCs), creatinine, triglycerides, low-density lipoprotein cholesterol (LDL-C), and high-density lipoprotein cholesterol (HDL-C) were obtained by laboratory measurements. Blood cell counts and hemoglobin levels were analyzed with the Beckman–Coulter MAXM or DXH 800. Albumin and creatinine were measured using the DcX800 method. Triglycerides and HDL-C were analyzed by the Roche/Hitachi Modular P Chemistry Analyzer (Mod P) in Mobile Examination Centers (MECs). LDL-C was calculated from measured values of triglycerides, HDL-C, and TC according to the Friedewald algorithm. Details on the methods are publicly available on the official NHANES website [18].

2.5. Statistical Analysis

All analyses were performed using Stata 17 (Stata Corp., Texas, USA). Multiple imputations (chained equations, 25 times) were used to fill in the missing values for all covariates. A trend test was used for the comparison of baseline characteristics between independent groups. Logistic regression models were used to assess the association between AAC and CHD. The model was progressively adjusted as follows: Model 1, unadjusted; Model 2, adjusted for age, sex, and ethnicity; Model 3, further adjusted for BMI, pulse, drinking, smoking, and DM; and Model 4, further adjusted for RBC, WBC, platelets, albumin, creatinine, triglyceride, LDL-C, and HDL-C. Restricted cubic spline curves (RCS) were used to explore possible nonlinear relationships between AAC and CHD. Subgroup analyses were performed to test whether the association between AAC and CHD was consistent in different subgroups. Sensitivity analyses tested whether the model was affected by treatment with antihypertensive drugs. All tests were two-sided. Statistical significance was considered when a p < 0.05.

3. Results

3.1. Baseline Characteristics

A total of 10,175 participants were initially included for potential analyses during the 2013–2014 NHANES survey cycle. After excluding participants who did not have essential hypertension (EH), were underage, or had missing data on CHD or AAC, 1565 patients with EH were finally analyzed in this study. Among these EH patients, there were 956 without AAC, 301 with mild AAC, 263 with moderate AAC, and 45 with severe AAC, as depicted in Figure 1. The prevalence of CHD was higher in the moderate AAC and severe AAC groups compared to the group without AAC (40.1% versus 30.9%, 47.7% versus 30.9%), as indicated in Table 1. Furthermore, EH patients with severe AAC were older, more likely to be former smokers, had a lower BMI, and had a higher prevalence of type 2 diabetes mellitus.

3.2. Association between AAC and CHD in EH on a Continuous Scale

On a continuous scale, each one-point increase in the AAC-24 score was associated with a 13% increase in the risk of coronary heart disease (CHD) prevalence, with an odds ratio (OR) of 1.13 (95% confidence interval [CI], 1.09–1.17) in the unadjusted model. This association remained significant even after adjusting for a broad spectrum of variables in the multivariable analysis. More detailed information can be found in Table 2.

3.3. Association between AAC and CHD in EH on a Categorical Scale

On a categorical scale, the results of the univariate analysis showed that the risk of coronary heart disease (CHD) prevalence was 1.26 (95% confidence interval [CI], 0.74–2.15) times higher for mild AAC, 3.96 (2.60–6.04) times higher for moderate AAC, and 5.74 (2.75–11.99) times higher for severe AAC, compared to individuals without AAC. The p-value for the trend was less than 0.001, indicating a significant relationship between AAC severity and CHD risk. These associations and trends remained significant even after adjusting for a broad spectrum of variables in the multivariable analysis. More information can be found in Table 2. The restricted cubic spline (RCS) curve analysis indicated a linear dose–response relationship between AAC severity and CHD risk in individuals with essential hypertension (EH), rather than a nonlinear relationship, as depicted in Figure 2.

3.4. Subgroup and Sensitivity Analysis

Subgroup analysis largely corroborated the associations between AAC and CHD in EH uncovered in the current study across a broad spectrum of risk factors, as depicted in Figure 3. The use of antihypertensive drugs may potentially influence abdominal aortic calcification. Therefore, we conducted a sensitivity analysis specifically within the population taking antihypertensive drugs. This did not alter our main findings, as demonstrated in Table 3. Additionally, our stratified analysis based on hypertension severity did not alter the results. Details can be found in Supplementary Tables S1 and S2.

4. Discussion

To the best of our knowledge, this is the first study examining the association between AAC and CHD in EH. The key findings of this study are that (i) a higher severity of AAC is associated with a higher risk of CHD prevalence in EH patients; and (ii) this association is displayed in a dose–response manner.
Arterial calcification stands out as a robust and independent risk factor for CHD [23]. This calcification process involves the deposition of hydroxyapatite crystals within the vasculature. Within the arterial wall, vascular smooth muscle cells (VSMCs) constitute the primary cell type, while elastin emerges as the predominant protein [24]. When the vascular wall is under oxidative stress [25], inflammation [26], apoptosis, aging [27], etc., the VSMC transdifferentiates to osteoblasts, and the elastin is lost in large quantities, which increases the expression of osteogenesis-related factors RUNX2 and BMP2 [28] and increases the occurrence of vascular calcification. Consequently, vascular calcification ensues, escalating arterial stiffness, pulse pressure, and left ventricular hypertrophy, culminating in CHD [29]. Our study underscores a significant association between AAC and CHD in patients with EH. In asymptomatic chronic dialysis patients, multifactorial regression analysis unveiled the AAC score as an independent predictor of CAD presence, with a 1.18-fold increased CAD risk per 1-point AAC score elevation [OR (95%CI), 1.18 (1.06–1.32)] [30]. Similarly, in type 2 diabetics, the prevalence of CHD was found to be twice as high in patients with AAC > 0 compared to those with AAC = 0 (28% versus 14%). Our study echoed these findings, revealing that patients with AAC (mild, moderate, and severe AACs) exhibited a 2.23-fold higher prevalence of CHD compared to those without AAC (69.1% versus 30.9%). Extensive research has underscored AAC as a significant cardiovascular disease risk factor in diabetic patients [31]. Parikh and colleagues observed a 2.1-fold increase in the odds of AAC in individuals with early-onset CHD within the third-generation population of the Framingham Heart Study, further supporting the association between AAC and heightened CHD risk [32]. Our study, encompassing a non-selective study population, bolsters the credibility of AAC-CHD associations. Additionally, while prior studies did not unveil the relationship between AAC and CHD in EH, a sole study found AAC to be independently linked to total CHD mortality in community-dwelling individuals [33]. Our findings suggest a linear association between AAC and CHD in EH, with elevated AAC scores correlating with heightened CHD prevalence.

Limitations

There are several limitations that warrant attention when interpreting our findings, as follows: (i) This study adopts the cross-sectional design, underscoring the necessity for further randomized, controlled trials to validate the relationship between AAC severity and CHD incidence. (ii) Certain factors potentially linked to coronary heart disease, such as sleep duration, exercise habits, thrombophilia, and cardiac arrhythmia, were not accounted for in our analysis. (iii) Some of the variables considered in this study, including smoking, alcohol consumption, hypertension, and diabetes mellitus, relied on subjective questionnaires, introducing the potential information bias.

5. Conclusions

In patients with EH, a higher severity of AAC is associated with a higher risk of CHD prevalence.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/jcdd11050143/s1. Table S1: Definition and grading of hypertension; Table S2: The association between AAC and CHD after stratification by the grade of hypertension.

Author Contributions

L.H. and X.L. wrote the main manuscript; E.S. and Y.-M.H. provided statistical guidance and were responsible for the final revisions. All authors have read and agreed to the published version of the manuscript.

Funding

National Key Research and Development Program of China (2021YFC2500600, 2021YFC2500602).

Institutional Review Board Statement

The NHANES database was deidentified and publicly available, and the study did not require institutional review board approval.

Informed Consent Statement

All participants involved in the data collection for the NHANES have signed informed consent forms.

Data Availability Statement

All data were obtained from the NHANES database (https://wwwn.cdc.gov/nchs/nhanes/Default.aspx, accessed on 15 June 2023).

Acknowledgments

We would like to thank the NHANES administration for providing publicly available data and reports that enabled us to prepare this paper.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Bonarjee, V.V.S. Arterial Stiffness: A Prognostic Marker in Coronary Heart Disease. Available Methods and Clinical Application. Front. Cardiovasc. Med. 2018, 5, 64. [Google Scholar] [CrossRef] [PubMed]
  2. Mortensen, M.B.; Dzaye, O.; Bodtker, H.; Steffensen, F.H.; Botker, H.E.; Jensen, J.M.; Ronnow Sand, N.P.; Maeng, M.; Warnakula Olesen, K.K.; Sorensen, H.T.; et al. Interplay of Risk Factors and Coronary Artery Calcium for CHD Risk in Young Patients. JACC Cardiovasc. Imaging 2021, 14, 2387–2396. [Google Scholar] [CrossRef] [PubMed]
  3. Polonskaya, Y.V.; Kashtanova, E.V.; Murashov, I.S.; Striukova, E.V.; Kurguzov, A.V.; Stakhneva, E.M.; Shramko, V.S.; Maslatsov, N.A.; Chernyavsky, A.M.; Ragino, Y.I. Association of Matrix Metalloproteinases with Coronary Artery Calcification in Patients with CHD. J. Pers. Med. 2021, 11, 506. [Google Scholar] [CrossRef] [PubMed]
  4. Zhang, H.; Li, G.; Yu, X.; Yang, J.; Jiang, A.; Cheng, H.; Fu, J.; Liang, X.; Liu, J.; Lou, J.; et al. Progression of Vascular Calcification and Clinical Outcomes in Patients Receiving Maintenance Dialysis. JAMA Netw. Open 2023, 6, e2310909. [Google Scholar] [CrossRef] [PubMed]
  5. Bastos Goncalves, F.; Voute, M.T.; Hoeks, S.E.; Chonchol, M.B.; Boersma, E.E.; Stolker, R.J.; Verhagen, H.J. Calcification of the abdominal aorta as an independent predictor of cardiovascular events: A meta-analysis. Heart 2012, 98, 988–994. [Google Scholar] [CrossRef] [PubMed]
  6. Criqui, M.H.; Denenberg, J.O.; McClelland, R.L.; Allison, M.A.; Ix, J.H.; Guerci, A.; Cohoon, K.P.; Srikanthan, P.; Watson, K.E.; Wong, N.D. Abdominal aortic calcium, coronary artery calcium, and cardiovascular morbidity and mortality in the Multi-Ethnic Study of Atherosclerosis. Arterioscler. Thromb. Vasc. Biol. 2014, 34, 1574–1579. [Google Scholar] [CrossRef] [PubMed]
  7. O’Connor, S.D.; Graffy, P.M.; Zea, R.; Pickhardt, P.J. Does Nonenhanced CT-based Quantification of Abdominal Aortic Calcification Outperform the Framingham Risk Score in Predicting Cardiovascular Events in Asymptomatic Adults? Radiology 2019, 290, 108–115. [Google Scholar] [CrossRef]
  8. Chen, H.C.; Wang, W.T.; Hsi, C.N.; Chou, C.Y.; Lin, H.J.; Huang, C.C.; Chang, C.T. Abdominal aortic calcification score can predict future coronary artery disease in hemodialysis patients: A 5-year prospective cohort study. BMC Nephrol. 2018, 19, 313. [Google Scholar] [CrossRef] [PubMed]
  9. Jurgens, P.T.; Carr, J.J.; Terry, J.G.; Rana, J.S.; Jacobs, D.R., Jr.; Duprez, D.A. Association of Abdominal Aorta Calcium and Coronary Artery Calcium with Incident Cardiovascular and Coronary Heart Disease Events in Black and White Middle-Aged People: The Coronary Artery Risk Development in Young Adults Study. J. Am. Heart Assoc. 2021, 10, e023037. [Google Scholar] [CrossRef]
  10. Slivnick, J.; Lampert, B.C. Hypertension and Heart Failure. Heart Fail. Clin. 2019, 15, 531–541. [Google Scholar] [CrossRef]
  11. Fuchs, F.D.; Whelton, P.K. High Blood Pressure and Cardiovascular Disease. Hypertension 2020, 75, 285–292. [Google Scholar] [CrossRef] [PubMed]
  12. Gao, Z.Y.; Xu, H.; Shi, D.Z.; Wen, C.; Liu, B.Y. Analysis on outcome of 5284 patients with coronary artery disease: The role of integrative medicine. J. Ethnopharmacol. 2012, 141, 578–583. [Google Scholar] [CrossRef] [PubMed]
  13. Stamler, J.; Stamler, R.; Neaton, J.D. Blood pressure, systolic and diastolic, and cardiovascular risks. US population data. Arch. Intern. Med. 1993, 153, 598–615. [Google Scholar] [CrossRef] [PubMed]
  14. Boutouyrie, P.; Chowienczyk, P.; Humphrey, J.D.; Mitchell, G.F. Arterial Stiffness and Cardiovascular Risk in Hypertension. Circ. Res. 2021, 128, 864–886. [Google Scholar] [CrossRef] [PubMed]
  15. Arribas, S.M.; Hinek, A.; Gonzalez, M.C. Elastic fibres and vascular structure in hypertension. Pharmacol. Ther. 2006, 111, 771–791. [Google Scholar] [CrossRef] [PubMed]
  16. Annes, J.P.; Munger, J.S.; Rifkin, D.B. Making sense of latent TGFbeta activation. J. Cell Sci. 2003, 116 Pt 2, 217–224. [Google Scholar] [CrossRef] [PubMed]
  17. Chen, N.X.; O’Neill, K.D.; Chen, X.; Moe, S.M. Annexin-mediated matrix vesicle calcification in vascular smooth muscle cells. J. Bone Miner. Res. 2008, 23, 1798–1805. [Google Scholar] [CrossRef] [PubMed]
  18. National Center for Health Statistics. Available online: https://www.cdc.gov/nchs/nhanes/index.htm (accessed on 20 June 2023).
  19. Kauppila, L.I.; Polak, J.F.; Cupples, L.A.; Hannan, M.T.; Kiel, D.P.; Wilson, P.W. New indices to classify location, severity and progression of calcific lesions in the abdominal aorta: A 25-year follow-up study. Atherosclerosis 1997, 132, 245–250. [Google Scholar] [CrossRef] [PubMed]
  20. Schousboe, J.T.; Wilson, K.E.; Hangartner, T.N. Detection of aortic calcification during vertebral fracture assessment (VFA) compared to digital radiography. PLoS ONE 2007, 2, e715. [Google Scholar] [CrossRef]
  21. Classification and Diagnosis of Diabetes: Standards of Medical Care in Diabetes—2022. Available online: https://www.diabetes.org/ (accessed on 15 June 2023).
  22. Definitions of Smoking and Drinking Status. Available online: https://www.health.govt.nz/ (accessed on 15 June 2023).
  23. Durham, A.L.; Speer, M.Y.; Scatena, M.; Giachelli, C.M.; Shanahan, C.M. Role of smooth muscle cells in vascular calcification: Implications in atherosclerosis and arterial stiffness. Cardiovasc. Res. 2018, 114, 590–600. [Google Scholar] [CrossRef]
  24. Lee, S.J.; Lee, I.K.; Jeon, J.H. Vascular Calcification-New Insights Into Its Mechanism. Int. J. Mol. Sci. 2020, 21, 2685. [Google Scholar] [CrossRef]
  25. Nguyen, N.T.; Nguyen, T.T.; Park, K.S. Oxidative Stress Related to Plasmalemmal and Mitochondrial Phosphate Transporters in Vascular Calcification. Antioxidants 2022, 11, 494. [Google Scholar] [CrossRef] [PubMed]
  26. Sanchez-Duffhues, G.; Garcia de Vinuesa, A.; van de Pol, V.; Geerts, M.E.; de Vries, M.R.; Janson, S.G.; van Dam, H.; Lindeman, J.H.; Goumans, M.J.; Ten Dijke, P. Inflammation induces endothelial-to-mesenchymal transition and promotes vascular calcification through downregulation of BMPR2. J. Pathol. 2019, 247, 333–346. [Google Scholar] [CrossRef] [PubMed]
  27. Pescatore, L.A.; Gamarra, L.F.; Liberman, M. Multifaceted Mechanisms of Vascular Calcification in Aging. Arterioscler. Thromb. Vasc. Biol. 2019, 39, 1307–1316. [Google Scholar] [CrossRef] [PubMed]
  28. Ahn, B.Y.; Jeong, Y.; Kim, S.; Zhang, Y.; Kim, S.W.; Leem, Y.E.; Kang, J.S. Cdon suppresses vascular smooth muscle calcification via repression of the Wnt/Runx2 Axis. Exp. Mol. Med. 2023, 55, 120–131. [Google Scholar] [CrossRef] [PubMed]
  29. Petsophonsakul, P.; Burgmaier, M.; Willems, B.; Heeneman, S.; Stadler, N.; Gremse, F.; Reith, S.; Burgmaier, K.; Kahles, F.; Marx, N.; et al. Nicotine promotes vascular calcification via intracellular Ca2+-mediated, Nox5-induced oxidative stress, and extracellular vesicle release in vascular smooth muscle cells. Cardiovasc. Res. 2022, 118, 2196–2210. [Google Scholar] [CrossRef] [PubMed]
  30. de Bie, M.K.; Buiten, M.S.; Rotmans, J.I.; Hogenbirk, M.; Schalij, M.J.; Rabelink, T.J.; Jukema, J.W. Abdominal aortic calcification on a plain X-ray and the relation with significant coronary artery disease in asymptomatic chronic dialysis patients. BMC Nephrol. 2017, 18, 82. [Google Scholar] [CrossRef] [PubMed]
  31. Wang, C.; Xie, Z.; Huang, X.; Wang, Z.; ShangGuan, H.; Wang, S. Prevalence of cardiovascular disease risk factors in Chinese patients with type 2 diabetes mellitus, 2013-2018. Curr. Med. Res. Opin. 2022, 38, 345–354. [Google Scholar] [CrossRef] [PubMed]
  32. Parikh, N.I.; Hwang, S.J.; Larson, M.G.; Cupples, L.A.; Fox, C.S.; Manders, E.S.; Murabito, J.M.; Massaro, J.M.; Hoffmann, U.; O’Donnell, C.J. Parental occurrence of premature cardiovascular disease predicts increased coronary artery and abdominal aortic calcification in the Framingham Offspring and Third Generation cohorts. Circulation 2007, 116, 1473–1481. [Google Scholar] [CrossRef]
  33. Han, D.; ó Hartaigh, B.; Gransar, H.; Lee, J.H.; Choi, S.Y.; Chun, E.J.; Sung, J.; Han, H.W.; Park, S.H.; Callister, T.; et al. Prevalence and Distribution of Coronary Artery Calcification in Asymptomatic United States and Korean Adults—Cross-Sectional Propensity-Matched Analysis. Circ. J. 2016, 80, 2349–2355. [Google Scholar] [CrossRef]
Jcdd 11 00143 g001
Figure 1. Flowchart of participant selection. Abbreviations: EH = essential hypertension; AAC = abdominal aortic calcification; and CHD = coronary heart disease.
Figure 1. Flowchart of participant selection. Abbreviations: EH = essential hypertension; AAC = abdominal aortic calcification; and CHD = coronary heart disease.
Jcdd 11 00143 g001
Jcdd 11 00143 g002
Figure 2. RCS curves for examining the nonlinear relationship between AAC score and CHD.
Figure 2. RCS curves for examining the nonlinear relationship between AAC score and CHD.
Jcdd 11 00143 g002
Jcdd 11 00143 g003
Figure 3. The results showed the OR (95% CI) of moderate AAC in different subgroups when without AAC was used as a reference. Subgroup analysis was adjusted for all variables as shown in Model 4 in Table 2. Abbreviations: OR = odds ratio; CI = confidence interval; and P-int = P-interaction.
Figure 3. The results showed the OR (95% CI) of moderate AAC in different subgroups when without AAC was used as a reference. Subgroup analysis was adjusted for all variables as shown in Model 4 in Table 2. Abbreviations: OR = odds ratio; CI = confidence interval; and P-int = P-interaction.
Jcdd 11 00143 g003
Table 1. Baseline characteristics stratified by AAC severity.
Table 1. Baseline characteristics stratified by AAC severity.
FactorWithout AAC
(n = 956)		Mild AAC
(n = 301)		Moderate AAC
(n = 263)		Severe AAC
(n = 45)		p for Trend
Age, year59.87 ± 10.8664.79 ± 10.0770.66 ± 9.5774.40 ± 6.69<0.001
Female486 (52.4%)152 (51.9%)136 (52.9%)24 (54.5%)0.842
Ethnicity 0.665
   Mexican American118 (12.7%)30 (10.2%)20 (7.8%)0 (0.0%)
   Non-Hispanic White340 (36.7%)147 (50.2%)149 (58.0%)30 (68.2%)
   Non-Hispanic Black274 (29.6%)59 (20.1%)41 (16.0%)7 (15.9%)
   Non-Hispanic Asian93 (10.0%)30 (10.2%)28 (10.9%)4 (9.1%)
   Others102 (11.0%)27 (9.2%)19 (7.4%)3 (6.8%)
BMI, kg/m2,30.12 ± 6.0528.43 ± 5.1527.55 ± 4.6727.16 ± 4.08<0.001
Pulse, beats/min72.11 ± 11.8371.61 ± 12.2469.23 ± 10.7769.80 ± 11.72<0.001
Drinking 0.806
   Never151 (16.3%)44 (15.0%)35 (13.6%)6 (13.6%)
   Former200 (21.6%)67 (22.9%)72 (28.0%)16 (36.4%)
   Current576 (62.1%)182 (62.1%)150 (58.4%)22 (50.0%)
Smoking 0.002
   Never521 (56.2%)143 (48.8%)111 (43.2%)18 (40.9%)
   Former251 (27.1%)98 (33.4%)87 (33.9%)20 (45.5%)
   Current155 (16.7%)52 (17.7%)59 (23.0%)6 (13.6%)
DM286 (30.9%)91 (31.1%)103 (40.1%)21 (47.7%)0.001
RBC, 103/μL4.62 ± 0.484.58 ± 0.4874.44 ± 0.494.23 ± 0.58<0.001
WBC, 103/μL7.18 ± 2.147.37 ± 2.117.37 ± 2.087.56 ± 2.280.217
Platelets, 103/μL233.82 ± 59.27225.16 ± 59.05220.05 ± 56.12213.40 ± 62.13<0.001
Albumin, g/L42.12 ± 3.1842.19 ± 3.1941.70 ± 3.1842.56 ± 3.530.381
Creatinine, umol/L85.62 ± 44.3490.48 ± 88.8497.95 ± 56.14106.52 ± 83.69<0.001
Triglycerides, mmol/L1.50± 0.891.51 ± 0.771.51 ± 0.731.44 ± 0.750.484
LDL-C, mmol/L2.94 ± 0.962.92 ± 1.022.75 ± 0.952.53 ± 0.92<0.001
HDL-C, mmol/L1.39 ± 0.431.35 ± 0.411.36 ± 0.381.39 ± 0.540.373
CHD286 (30.9%)91 (31.1%)103 (40.1%)21 (47.7%)<0.001
Notes: continuous and categorical variables were presented as mean ± SD or percentages n (%), respectively. BMI = body mass index; DM = diabetes mellitus; RBC = red blood cell; WBC = white blood cell; LDL-C = low-density lipoprotein cholesterol; HDL-C = high-density lipoprotein cholesterol; and CHD = coronary heart disease.
Table 2. ORs and 95% confidence intervals for the association between AAC and CHD in EH.
Table 2. ORs and 95% confidence intervals for the association between AAC and CHD in EH.
AAC ScoreModel 1Model 2Model 3Model 4
OR (95% CI)OR (95% CI)OR (95% CI)OR (95% CI)
Continuous per score increase1.13 (1.09–1.17) 1.09 (1.05–1.13)1.08 (1.04–1.12) 1.07 (1.03–1.11)
Categorical per unit increase
Without AAC (0)1 (Ref.)1 (Ref.)1 (Ref.)1 (Ref.)
Mild AAC (1–4)1.26 (0.74–2.15)1.03 (0.59–1.78)1.08 (0.61–1.88)1.09 (0.61–1.95)
Moderate AAC (5–15)3.96 (2.60–6.04)2.47 (1.53–3.97)2.24 (1.37–3.67)2.06 (1.23–3.45)
Severe AAC (6–24)5.74 (2.75–11.99)2.93 (1.29–6.59)2.62 (1.13–6.05)2.18 (1.09–5.25)
Model 1: unadjusted. Model 2: adjusted for age, sex, and ethnicity. Model 3: further adjusted for BMI, pulse, drinking, smoking, and DM. Model 4: further adjusted for RBC, WBC, platelets, albumin, creatinine, triglyceride, LDL-C, and HDL-C. Abbreviations: AAC = abdominal aortic calcification; OR = odds ratio; and CI = confidence interval.
Table 3. ORs and 95% confidence intervals for the association between AAC and CHD in EH patients taking antihypertensive drugs.
Table 3. ORs and 95% confidence intervals for the association between AAC and CHD in EH patients taking antihypertensive drugs.
AAC ScoreModel 1Model 2Model 3Model 4
OR (95% CI)OR (95% CI)OR (95% CI)OR (95% CI)
Continuous per score increase1.10 (1.08–1.15) 1.08 (1.04–1.12)1.07 (1.0–1.12) 1.06 (1.02–1.11)
Categorical per unit increase
Without AAC (0)1 (Ref.)1 (Ref.)1 (Ref.)1 (Ref.)
Mild AAC (1–4)1.16 (0.64–2.08)1.04 (0.57–1.91)1.05 (0.57–1.94)1.08 (0.57–2.02)
Moderate AAC (5–15)3.78 (2.40–5.96)2.64 (1.57–4.41)2.36 (1.38–4.04)2.32 (1.33–4.06)
Severe AAC (6–24)5.58 (2.60–11.97)3.25 (1.39–7.58)2.83 (1.19–6.74)2.50 (1.01–6.19)
Model 1: unadjusted. Model 2: adjusted for age, sex, and ethnicity. Model 3: further adjusted for BMI, pulse, drinking, smoking, and DM. Model 4: further adjusted for RBC, WBC, platelets, albumin, creatinine, triglyceride, LDL-C, and HDL-C. Abbreviations: AAC = abdominal aortic calcification; OR = odds ratio; and CI = confidence interval.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

He, L.; Li, X.; Shen, E.; He, Y.-M. Association between Abdominal Aortic Calcification and Coronary Heart Disease in Essential Hypertension: A Cross-Sectional Study from the 2013–2014 National Health and Nutrition Examination Survey. J. Cardiovasc. Dev. Dis. 2024, 11, 143. https://doi.org/10.3390/jcdd11050143

AMA Style

He L, Li X, Shen E, He Y-M. Association between Abdominal Aortic Calcification and Coronary Heart Disease in Essential Hypertension: A Cross-Sectional Study from the 2013–2014 National Health and Nutrition Examination Survey. Journal of Cardiovascular Development and Disease. 2024; 11(5):143. https://doi.org/10.3390/jcdd11050143

Chicago/Turabian Style

He, Lan, Xu Li, E Shen, and Yong-Ming He. 2024. "Association between Abdominal Aortic Calcification and Coronary Heart Disease in Essential Hypertension: A Cross-Sectional Study from the 2013–2014 National Health and Nutrition Examination Survey" Journal of Cardiovascular Development and Disease 11, no. 5: 143. https://doi.org/10.3390/jcdd11050143

APA Style

He, L., Li, X., Shen, E., & He, Y. -M. (2024). Association between Abdominal Aortic Calcification and Coronary Heart Disease in Essential Hypertension: A Cross-Sectional Study from the 2013–2014 National Health and Nutrition Examination Survey. Journal of Cardiovascular Development and Disease, 11(5), 143. https://doi.org/10.3390/jcdd11050143

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop