The relationship among hypertension, antihypertensive medications, and osteoporosis: a narrative review.
Study Goal
The researchers aimed to examine the role of high sodium salt consumption in the etiology of hypertension and osteoporosis, and its interaction with antihypertensive drugs.
Results Summary
High consumption of sodium salt was identified as a relevant nongenetic factor contributing to both hypertension and osteoporosis, though the study did not quantify its direct effects. The impact of salt on bone mineral density was discussed in the context of antihypertensive therapy, with mixed findings.
Population
Aging population with hypertension and/or osteoporosis.
Effective Dosage
Not specified
Duration
Not specified
Interactions
Thiazide diuretics were noted to have a positive influence on bone mineral density, while other antihypertensives showed conflicting effects.
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
treatment of hypertension | neutral | bone mineral density | - | - | affects | #1 |
treatment of hypertension | increase | osteoporosis | - | - | can worsen | #2 |
low calcium intake | neutral | etiology of osteoporosis and hypertension | - | - | relevant nongenetic factor | #3 |
vitamin D deficiency | neutral | etiology of osteoporosis and hypertension | - | - | relevant nongenetic factor | #4 |
vitamin K deficiency | neutral | etiology of osteoporosis and hypertension | - | - | relevant nongenetic factor | #5 |
high consumption of sodium salt | neutral | etiology of osteoporosis and hypertension | - | - | relevant nongenetic factor | #6 |
effects of different forms of nitric oxide | neutral | etiology of osteoporosis and hypertension | - | - | relevant nongenetic factor | #7 |
Thiazide diuretics | increase | bone mineral density | - | - | have a positive influence on | #8 |
other antihypertensive drugs | neutral | bone mineral density | - | - | may have a potentially negative or positive influence on | #9 |
other antihypertensive drugs | neutral | fracture risk reduction | - | - | may have a potentially negative or positive influence on | #10 |
use of antihypertensives | no change | bone mineral density | - | - | did not find a correlation | #11 |
antihypertensive drugs | neutral | osteoporosis | patients with frequent coexistence of hypertension and osteoporosis | - | potential effects on development, worsening, or improvement of | #12 |
Osteoporosis and hypertension are two frequent diseases among the aging population that share a similar etiopathology and often coexist. Moreover, treatment of hypertension affects bone mineral density and, therefore, can worsen osteoporosis. This narrative review considers the influence of the main etiologic factors that contribute to the development of hypertension and osteoporosis and examines the effect of the most often used antihypertensives on bones. A computerized literature search of relevant English publications regarding the etiology of hypertension and osteoporosis as well as the impact of antihypertensives on osteoporosis from 1996 to 2011 was completed in October 2011. The latest update in the search was performed from May to June 2012. The most relevant nongenetic factors in the etiology of osteoporosis and hypertension are low calcium intake, vitamin D and vitamin K deficiency, high consumption of sodium salt, and the effects of different forms of nitric oxide. Thiazide diuretics are the only antihypertensives that have a positive influence on bone mineral density. For other antihypertensive drugs, the data are conflicting, indicating that they may have a potentially negative or positive influence on bone mineral density and fracture risk reduction. Some studies did not find a correlation between the use of antihypertensives and bone mineral density. Due to the frequent coexistence of hypertension and osteoporosis, when selecting long-term antihypertensive therapy the potential effects of antihypertensive drugs on development, worsening, or improvement of osteoporosis should also be considered.