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The relationship between hypertension and thoracic spine bone mineral density: the Multi-Ethnic Study of
Ahmed K Ghanem1,2, Venkat S Manubolu3, April Kinninger3
1Lundquist Institute, Harbor-UCLA Medical Center, Torrance, CA, USA. aghanem@llu.edu.
Insights
Hypertension (high blood pressure) is not independently linked to lower bone mineral density (BMD), the measure for osteoporosis risk. This study found no significant association after accounting for other factors.
Area of Science:
- Cardiovascular Health
- Bone Metabolism
- Immunology
Background:
- Hypertension (HTN) and osteoporosis (low bone mineral density, BMD) were historically considered separate conditions.
- Emerging research suggests shared pathways involving vascular inflammation and immune cell activation.
- The precise relationship between HTN and BMD remains unclear.
Purpose of the Study:
- To investigate the association between hypertension and bone mineral density.
- To determine if hypertension is an independent risk factor for lower BMD.
Main Methods:
- Utilized data from 6,814 MESA study participants.
- Measured thoracic spine BMD using non-contrast CT scans.
- Employed linear and logistic regression, adjusting for age, gender, race/ethnicity, BMI, and osteoporosis medication use.
Main Results:
- Unadjusted analysis showed higher osteoporosis prevalence and lower BMD in hypertensive individuals.
- After adjusting for confounders, the association between HTN and BMD was not statistically significant (p=0.687).
- Higher BMD was observed in Black, Chinese, and Hispanic participants compared to White participants; higher BMI and younger age correlated with increased BMD.
Conclusions:
- Hypertension does not appear to be independently associated with bone mineral density.
- Other factors like race/ethnicity, BMI, and age significantly influence BMD.
Purpose/Introduction:
Historically, hypertension (HTN) and osteoporosis, as indicated by bone mineral density (BMD), were viewed as distinct conditions. However, current understanding highlights the role of vascular inflammation and immune cell activation in both diseases. The exact relationship between HTN and BMD, however, remains poorly defined.
Methods:
Participants from the MESA study, both with and without hypertension (defined as systolic blood pressure ≥ 140 mmHg and/or diastolic blood pressure ≥ 90 mmHg, or the use of antihypertensive drugs), underwent thoracic spine BMD measurement using non-contrast CT chest. Linear regression was used to assess the relationship between BMD and HTN. BMD was also categorized by T-scores (normal, osteopenia, osteoporosis) and analyzed using proportional odds logistic regression. The models were adjusted for variables such as age, gender, race/ethnicity, BMI, and osteoporosis medication use to assess these associations.
Results:
Among the 6,814 participants, those with hypertension (HTN) were older and more likely to be Black and female. Osteoporosis was more prevalent among hypertensive individuals (30% vs. 23%), with a lower mean BMD by 6.23 mg/cc in unadjusted analysis (p < 0.001). However, after adjusting for confounders, the association between HTN and BMD was not significant (p = 0.687). In adjusted models, Black, Chinese, and Hispanic participants had significantly higher BMD compared to White participants. Additionally, higher BMI was associated with increased BMD, while older age was associated with lower BMD.
Conclusion:
The findings indicate that hypertension does not have an independent association with BMD.
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