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
. 2022 Aug 7;5(5):e732.
doi: 10.1002/hsr2.732. eCollection 2022 Sep.

Low bone mineral density and its related factors in adults with congenital heart disease in Vietnam: A cross-sectional study

Affiliations

Low bone mineral density and its related factors in adults with congenital heart disease in Vietnam: A cross-sectional study

Thanh-Huong Truong et al. Health Sci Rep. .

Abstract

Background and aims: Recent studies have highlighted the increased risk of low bone mineral density (BMD) in adults with cardiovascular disease. However, little is known about BMD in adults with congenital heart disease (CHD), particularly in developing countries. We hypothesized that factors related to BMD would lead to a high prevalence of low BMD in adults with CHD. This study aimed to determine the prevalence of low BMD and its related factors in Vietnamese adults with CHD.

Methods: We conducted a cross-sectional study of 73 adults diagnosed with CHD in Vietnam. Low BMD was classified based on their site-specific Z-scores and T-scores at the posteroanterior lumbar spine and left proximal femur. Logistic regression analyses were performed to evaluate factors related to low BMD.

Results: Low BMD was confirmed in one-third of the adults with CHD. There were trends of more bone loss in certain parts of the body than in others, with the prevalence of low BMD at the sites of the lumbar vertebrae (L1‒L4) and left proximal femur (femoral neck, trochanteric femur, and intertrochanteric area) of 43.9%, 31.8%, 28.8%, 33.3%, 8.8%, 1.5%, and 6.1%, respectively. The prevalence of low BMD in the lumbar spine was significantly higher than that in the left proximal femur (34.3% vs. 2.9%, p < 0.001). Moreover, the prevalence of low BMD was significantly higher in adults with CHD than in those without polycythemia and vitamin D deficiency (55.6% vs. 20.9%, p = 0.001 and 46.2% vs. 19.4%, p = 0.002, respectively). A stratified multivariate logistic regression analysis revealed that low BMD was associated with polycythemia (odds ratio: 4.72; 95% confidence interval: 1.64-13.58, p = 0.004).

Conclusions: Low BMD is common among adults with CHD in Vietnam and related to polycythemia.

Keywords: bone mineral density; cardiovascular disease; congenital heart disease; polycyemia.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Prevalence of low bone mineral density (BMD) in adults with congenital heart disease, using χ 2 test. L, lumbar vertebrae.
Figure 2
Figure 2
Prevalence of low bone mineral density for whole body by subgroups in adults with congenital heart disease, using χ 2 test or *Fisher's exact test. NYHA, New York Association; PAH, pulmonary artery hypertension.

Similar articles

Cited by

References

    1. Liu Y, Chen S, Zühlke L, et al. Global birth prevalence of congenital heart defects 1970‐2017: updated systematic review and meta‐analysis of 260 studies. Int J Epidemiol. 2019;48:455‐463. - PMC - PubMed
    1. Lui GK, Saidi A, Bhatt AB, et al. Diagnosis and management of noncardiac complications in adults with congenital heart disease: a scientific statement from the American heart association. Circulation. 2017;136:e348‐e392. - PubMed
    1. Cheng HH, Carmona F, McDavitt E, et al. Fractures related to metabolic bone disease in children with congenital heart disease. Congenit Heart Dis. 2016;11:80‐86. - PubMed
    1. Sözen T, Özışık L, Başaran NÇ. An overview and management of osteoporosis. Eur J Rheumatol. 2017;4:46‐56. - PMC - PubMed
    1. Cauley JA. Public health impact of osteoporosis. J Gerontol A Biol Sci Med Sci. 2013;68:1243‐1251. - PMC - PubMed

LinkOut - more resources