Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Jan 3;24(1):26.
doi: 10.1186/s12872-023-03700-2.

Association between hemoglobin A1c and abdominal aortic calcification: results from the National Health and Nutrition Examination Survey 2013-2014

Affiliations

Association between hemoglobin A1c and abdominal aortic calcification: results from the National Health and Nutrition Examination Survey 2013-2014

Can Cai et al. BMC Cardiovasc Disord. .

Abstract

Background: Hemoglobin A1c (HbA1c), a "gold standard" for the assessment of glycemic control, was associated with an increased risk of cardiovascular disease and coronary artery calcification. However, its effects on abdominal aortic calcification (AAC) are uncertain. The present study comprehensively investigated the association between HbA1c and AAC in the 2013-2014 National Health and Nutrition Examinations Surveys.

Methods: Among 1,799 participants ≥ 40 years, dual-energy X-ray absorptiometry-derived AAC was quantified using the Kauppila score (AAC-24). Severe AAC was defined as a total AAC-24 > 6. Weighted linear regression models and logistic regression models were used to determine the effects of HbA1c on AAC. The restricted cubic spline model was used for the dose-response analysis.

Results: The mean AAC-24 of participants was 1.3, and 6.7% of them suffered from severe AAC. Both AAC-24 and the prevalence of severe AAC increased with the higher tertile of HbA1c (P < 0.001). Elevated HbA1c levels would increase the AAC-24 (β = 0.73, 95% CI: 0.30-1.16) and the risk of severe AAC (OR = 1.63, 95% CI: 1.29-2.06), resulting in nearly linear dose-response relationships in all participants. However, this positive correlation were not statistically significant when participants with diabetes were excluded. Furthermore, subgroup analysis showed significant interactions effect between HbA1c and hypertension on severe AAC with the OR (95% CI) of 2.35 (1.62-3.40) for normotensives and 1.39 (1.09-1.79) for hypertensives (P for interaction = 0.022).

Conclusion: Controlling HbA1c could reduce AAC scores and the risk of severe AAC. Glycemic management might be a component of strategies for preventing AAC among all participants, especially normotensives.

Keywords: Abdominal aortic calcification; Cross-sectional study; Hemoglobin A1c; NHANES.

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
Flowchart of participant selection NHANES, National Health and Nutrition Examination Survey; AAC, abdominal aortic calcification, HbA1c, hemoglobin A1c
Fig. 2
Fig. 2
Subgroup analysis for the association between HbA1c level as a continuous variable and severe AAC. Odds ratio adjusted for variables in the Model 3 (age, gender, BMI, race, education level, RIP, smoking status, alcohol drinking status, metabolic equivalent, SBP, TC, eGFR, total 25-hydroxyvitamin D, serum calcium, serum phosphorus, and NLR) except the corresponding stratification variable OR: odds ratio; CI, confidence interval; BMI, body mass index; HbA1c, hemoglobin A1c
Fig. 3
Fig. 3
Dose-response relation between hemoglobin A1c level and AAC. a, Dose-response relation between hemoglobin A1c level and AAC-24 score; b, Dose-response relation between hemoglobin A1c level and severe AAC. The restricted cubic spline model was adjusted by age, gender, BMI, race, education level, RIP, smoking status, alcohol drinking status, metabolic equivalent, SBP, TC, eGFR, total 25-hydroxyvitamin D, serum calcium, serum phosphorus, and NLR. AAC, abdominal aortic calcification, HbA1c, hemoglobin A1c

Similar articles

Cited by

References

    1. GBD 2019 Diseases and Injuries Collaborators Global burden of 369 Diseases and injuries in 204 countries and territories, 1990–2019: a systematic analysis for the global burden of Disease Study 2019. Lancet. 2020;396(10258):1204–22. doi: 10.1016/S0140-6736(20)30925-9. - DOI - PMC - PubMed
    1. Roth GA, Johnson C, Abajobir A, Abd-Allah F, Abera SF, Abyu G, Ahmed M, Aksut B, Alam T, Alam K, et al. Global, Regional, and National Burden of Cardiovascular Diseases for 10 causes, 1990 to 2015. J Am Coll Cardiol. 2017;70(1):1–25. doi: 10.1016/j.jacc.2017.04.052. - DOI - PMC - PubMed
    1. Jebari-Benslaiman S, Galicia-García U, Larrea-Sebal A, Olaetxea JR, Alloza I, Vandenbroeck K, Benito-Vicente A, Martín C. Pathophysiology of Atherosclerosis. Int J Mol Sci 2022, 23(6). - PMC - PubMed
    1. Allam AHA, Thompson RC, Eskander MA, Mandour Ali MA, Sadek A, Rowan CJ, Sutherland ML, Sutherland JD, Frohlich B, Michalik DE, et al. Is coronary calcium scoring too late? Total body arterial calcium burden in patients without known CAD and normal MPI. J Nucl Cardiol. 2018;25(6):1990–8. doi: 10.1007/s12350-017-0925-9. - DOI - PubMed
    1. Wong ND, Lopez VA, Allison M, Detrano RC, Blumenthal RS, Folsom AR, Ouyang P, Criqui MH. Abdominal aortic calcium and multi-site Atherosclerosis: the multiethnic study of Atherosclerosis. Atherosclerosis. 2011;214(2):436–41. doi: 10.1016/j.atherosclerosis.2010.09.011. - DOI - PMC - PubMed

MeSH terms

Substances

LinkOut - more resources