维生素D与高血压:有显著关系吗?

Naga P. Vakkalagadda, Sri H. Narayana, Gummadi S. Sree, Lakshmi D. Bethineedi, L. V. Simhachalam Kutikuppala, Gnana D. Medarametla
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However, since the exact origin of PH and its pathophysiology are unknown, less effective, and generic treatments are used.<span><sup>2</sup></span> The fact that more than 50% of hypertension patients in the USA do not have their BP under good control serves as an illustration of this. Antihypertensive treatment resistance affects an additional 5 million people and is defined as the inability to regulate BP despite the use of at least three antihypertensive drugs in combination.<span><sup>3</sup></span></p><p>Increasing age, racial variables, history in household members, obese status, physical inactivity, larger amounts of salt consumption, stress, tobacco use, and heavy alcohol use are some of the potential etiological factors for essential hypertension.<span><sup>4</sup></span> It has been examined in previous meta-analyses how vitamin D supplementation affects BP,<span><sup>5</sup></span> but it is still unclear whether this connection is causal in the general population. This study focused on finding out the effect of vitamin D3 deficiency on BP.</p><p>Vitamin D, a steroid hormone, promotes the calcium and phosphate absorption from the gastro-intestinal tract (GIT) and reabsorption from the renal tubules. At low levels, it causes bone mineralization. At high doses, it causes bone resorption. It contributes significantly to mineral metabolism and skeletal homeostasis in this way.<span><sup>3</sup></span></p><p>Up to 80% of human vitamin D comes from vitamin D3, which is produced in the skin by ultraviolet (UV) radiation from 7-dehydrocholesterol. Fish, egg yolk, fortified milk, cereal, juice, and yogurt are dietary sources of vitamin D that provide D2 as well as D3 forms and account for around 20% of the body's requirement. The significant vitamin D form, 25-hydroxyvitamin D [25(OH)D], is produced by the liver from D2 and D3 forms of vitamin D in the body. It is the most accurate measure of the action status and levels of vitamin D. It mostly depends on the serum vitamin D binding protein.<span><sup>4</sup></span></p><p>According to the Institution of Endocrinology clinical practice guidelines, blood 25-hydroxyvitamin D [25(OH)D] results below 20 ng/mL (or 50 nmol/L) are considered deficient levels of vitamin D. Inadequate vitamin D status is ubiquitous among Chinese.<span><sup>4</sup></span> Numerous studies have been published describing how vitamin D deficiency can lead to cancer,<span><sup>6-10</sup></span> metabolic disorders, and cardiovascular disease. It has been shown to be negatively correlated with risk. It has been hypothesized that fluctuations in BP may be related to vitamin D administration among individuals with deficient levels of vitamin D.<span><sup>11</sup></span> Regular vitamin D provision can lower levels of blood-pressure in patients with low levels of vitamin D, without the need for high doses of medication. It may be a simple cure for what can become a chronic condition.<span><sup>12</sup></span></p><p>Every 10% rise in 25-hydroxyvitamin D concentration was found to result in an 8.1% reduction in the risk of hypertension.<span><sup>13</sup></span> Researchers are considering further research into how Vitamin D deficiency may affect other risk factors for heart disease, such as the likelihood of Type 2 diabetes and high cholesterol, after discovering this potentially significant association.</p><p>To date, over several randomized clinical trials have been organized by researchers to determine whether vitamin D administration lowers BP and determine its role as a prevention strategy.<span><sup>14-16</sup></span> The results of these studies are mixed, as they demonstrate an unsatisfactory design, and the mechanisms underlying how vitamin D affects hypertension remain to be deciphered. Therefore, many meta-analytical studies have attempted to integrate previous results and thereby assess the functional relation of vitamin D administration in regulating BP.<span><sup>4</sup></span></p><p>A meta analysis published earlier by Zhang et al.<span><sup>15</sup></span> has found that the risk of hypertension was significantly increased when 25(OH)D was reduced below 75 nmol/L, but continued to be prominent in the 75–130 nmol/L range. BP is approximately L-shaped (nonlinearity = 0.04). However, aggregated data showed that neither systolic nor diastolic BP was significantly reduced after the vitamin D intervention.</p><p>Primary hypertension is caused by many factors that interact with aging by means of hereditary and ecological determinants. Although vitamin D deficit promotes increased vascular tone,<span><sup>16</sup></span> it may not be a significant environmental factor in regulating normal BP homeostasis, but it does impair the causation of primary HTN among susceptible adult individuals, which works as a catalyst.<span><sup>16, 17</sup></span> Other noteworthy hypotheses have indicated that vitamin D alters vascular endothelial function or VSM intracellular calcium concentrations. This is the most notable mechanism linking vitamin D to hypertension.<span><sup>18</sup></span> The enhanced renin-angiotensin-aldosterone system (RAAS) activity and improvement in hypertension observed in studies with vitamin D receptor (VDR) knockout mice point to a critical role for vitamin D as a potential antihypertensive medication.<span><sup>19</sup></span></p><p>Studies conducted previously have been shown to bring inconsistent results. The information presented in this context gives a conclusion accordingly in a cohort of vitamin D-deficient hypertensive patients, moderately high doses containing vitamin D will either restore or close to physiological blood 25(OH)D levels and prominently decrease BP. Surprisingly, some studies failed to observe an improving effect of vitamin D on BP. However, the contradicting results may be due to poor research methods, confounding role of other anti-hypertensive agents, and &lt;10 cohorts. Forty percent of people have vitamin D deficiency along with having either extremely low or increased levels of intaking vitamin D. In normotensive subjects with or without vitamin D, there was little effect on BP.<span><sup>17</sup></span></p><p>However, from a 5-year VITAL experiment, supplementing a cohort of people at ages likely to develop vitamin D deficiency levels with high regular amounts of intake of vitamin D reduced hypertension, which may be circumvented. This VITAL study has also found a reduction in cancer-related risks, apart from reducing hypertension.<span><sup>12</sup></span></p><p>Advances in clinical research coupled with detailed mechanistic studies may pave the way for large-scale clinical trials conducted in specific demographic groups. The public health burden of managing PH is reduced when vitamin D supplements are administered to the population, reducing the public health burden and helping to dramatically improve clinical practice of PH interventions. Physicians are also encouraged to check their patients' vitamin D levels to help control increasingly frequent high BP.</p><p>Naga P. Vakkalagadda: Conceptualization; manuscript writing and editing. Sri H. Narayana: Conceptualization; manuscript writing and editing. Gummadi S. Sree: Manuscript writing and editing. Lakshmi D. Bethineedi: Manuscript writing and editing. L. V. Simhachalam Kutikuppala: Manuscript writing and editing; submission. Gnana D. 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Antihypertensive treatment resistance affects an additional 5 million people and is defined as the inability to regulate BP despite the use of at least three antihypertensive drugs in combination.<span><sup>3</sup></span></p><p>Increasing age, racial variables, history in household members, obese status, physical inactivity, larger amounts of salt consumption, stress, tobacco use, and heavy alcohol use are some of the potential etiological factors for essential hypertension.<span><sup>4</sup></span> It has been examined in previous meta-analyses how vitamin D supplementation affects BP,<span><sup>5</sup></span> but it is still unclear whether this connection is causal in the general population. This study focused on finding out the effect of vitamin D3 deficiency on BP.</p><p>Vitamin D, a steroid hormone, promotes the calcium and phosphate absorption from the gastro-intestinal tract (GIT) and reabsorption from the renal tubules. At low levels, it causes bone mineralization. At high doses, it causes bone resorption. It contributes significantly to mineral metabolism and skeletal homeostasis in this way.<span><sup>3</sup></span></p><p>Up to 80% of human vitamin D comes from vitamin D3, which is produced in the skin by ultraviolet (UV) radiation from 7-dehydrocholesterol. Fish, egg yolk, fortified milk, cereal, juice, and yogurt are dietary sources of vitamin D that provide D2 as well as D3 forms and account for around 20% of the body's requirement. The significant vitamin D form, 25-hydroxyvitamin D [25(OH)D], is produced by the liver from D2 and D3 forms of vitamin D in the body. It is the most accurate measure of the action status and levels of vitamin D. It mostly depends on the serum vitamin D binding protein.<span><sup>4</sup></span></p><p>According to the Institution of Endocrinology clinical practice guidelines, blood 25-hydroxyvitamin D [25(OH)D] results below 20 ng/mL (or 50 nmol/L) are considered deficient levels of vitamin D. Inadequate vitamin D status is ubiquitous among Chinese.<span><sup>4</sup></span> Numerous studies have been published describing how vitamin D deficiency can lead to cancer,<span><sup>6-10</sup></span> metabolic disorders, and cardiovascular disease. It has been shown to be negatively correlated with risk. It has been hypothesized that fluctuations in BP may be related to vitamin D administration among individuals with deficient levels of vitamin D.<span><sup>11</sup></span> Regular vitamin D provision can lower levels of blood-pressure in patients with low levels of vitamin D, without the need for high doses of medication. It may be a simple cure for what can become a chronic condition.<span><sup>12</sup></span></p><p>Every 10% rise in 25-hydroxyvitamin D concentration was found to result in an 8.1% reduction in the risk of hypertension.<span><sup>13</sup></span> Researchers are considering further research into how Vitamin D deficiency may affect other risk factors for heart disease, such as the likelihood of Type 2 diabetes and high cholesterol, after discovering this potentially significant association.</p><p>To date, over several randomized clinical trials have been organized by researchers to determine whether vitamin D administration lowers BP and determine its role as a prevention strategy.<span><sup>14-16</sup></span> The results of these studies are mixed, as they demonstrate an unsatisfactory design, and the mechanisms underlying how vitamin D affects hypertension remain to be deciphered. 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Although vitamin D deficit promotes increased vascular tone,<span><sup>16</sup></span> it may not be a significant environmental factor in regulating normal BP homeostasis, but it does impair the causation of primary HTN among susceptible adult individuals, which works as a catalyst.<span><sup>16, 17</sup></span> Other noteworthy hypotheses have indicated that vitamin D alters vascular endothelial function or VSM intracellular calcium concentrations. This is the most notable mechanism linking vitamin D to hypertension.<span><sup>18</sup></span> The enhanced renin-angiotensin-aldosterone system (RAAS) activity and improvement in hypertension observed in studies with vitamin D receptor (VDR) knockout mice point to a critical role for vitamin D as a potential antihypertensive medication.<span><sup>19</sup></span></p><p>Studies conducted previously have been shown to bring inconsistent results. 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引用次数: 0

摘要

全世界约有十亿人患有高血压。1 血压(BP)的调节涉及许多信号通路。其中,肾素血管紧张素系统是众所周知的。所有这些途径都通过调节肾盐处理和血管平滑肌(VSM)组织的张力来调节。这些机制中的任何一个都可能出现问题,并改变阻力动脉的血管平滑肌张力,从而导致血压升高。然而,由于 PH 的确切病因及其病理生理学尚不清楚,因此采用的治疗方法效果较差,而且是普通的治疗方法2。抗高血压治疗耐药性影响着另外 500 万人,其定义是,尽管联合使用了至少三种抗高血压药物,但仍无法控制血压。年龄增长、种族变量、家庭成员病史、肥胖状况、缺乏运动、食盐摄入量增加、压力、吸烟和大量饮酒是导致原发性高血压的一些潜在病因。维生素 D 是一种类固醇激素,可促进胃肠道(GIT)对钙和磷酸盐的吸收以及肾小管对钙和磷酸盐的重吸收。低剂量时,它能促进骨骼矿化。高剂量时,它会导致骨吸收。3 人体中高达 80% 的维生素 D 来自维生素 D3,它是在皮肤中通过紫外线(UV)辐射从 7-脱氢胆固醇中产生的。鱼类、蛋黄、强化牛奶、谷物、果汁和酸奶都是维生素 D 的膳食来源,可提供 D2 和 D3 两种形式,约占人体需要量的 20%。重要的维生素 D 形式--25-羟基维生素 D [25(OH)D],是由肝脏从体内的 D2 和 D3 形式维生素 D 生成的。4 根据美国内分泌学会的临床实践指南,血液中 25- 羟维生素 D [25(OH)D] 结果低于 20 ng/mL(或 50 nmol/L)即被视为维生素 D 缺乏。研究表明,维生素 D 与风险呈负相关。11 定期补充维生素 D 可以降低维生素 D 水平低的患者的血压水平,而无需服用大剂量药物。12 研究发现,25-羟基维生素 D 浓度每增加 10%,患高血压的风险就会降低 8.1%。迄今为止,研究人员已组织了多项随机临床试验,以确定服用维生素 D 是否能降低血压并确定其作为预防策略的作用。14-16 这些研究的结果好坏参半,因为它们的设计并不令人满意,维生素 D 影响高血压的机制仍有待破解。因此,许多荟萃分析研究试图整合之前的研究结果,从而评估服用维生素 D 在调节血压方面的功能关系。4 Zhang 等人早些时候发表的荟萃分析15 发现,当 25(OH)D 降低到 75 nmol/L 以下时,高血压的风险会显著增加,但在 75-130 nmol/L 的范围内,高血压的风险仍然突出。血压近似于 L 型(非线性 = 0.04)。然而,综合数据显示,维生素 D 干预后,收缩压和舒张压均未显著降低。原发性高血压由多种因素引起,这些因素通过遗传和生态决定因素与衰老相互作用。虽然维生素 D 的缺乏会促进血管张力的增加,16 但它可能并不是调节正常血压平衡的重要环境因素,但它确实会损害易感成人原发性高血压的病因,从而起到催化剂的作用。
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Vitamin D and hypertension: Is there any significant relation?

Around a billion individuals worldwide have hypertension. Of these, 95% have essential hypertension, a type of undiagnosed hypertension.1 The regulation of blood pressure (BP) involves numerous signaling pathways. Among them, the Renin Angiotensin System is well known. All these pathways are regulated by modulation of renal salt handling and tone of vascular smooth muscle (VSM) tissue. Any of these mechanisms can become faulty and alter the resistance arteries’ VSM tone, which can elevate BP. However, since the exact origin of PH and its pathophysiology are unknown, less effective, and generic treatments are used.2 The fact that more than 50% of hypertension patients in the USA do not have their BP under good control serves as an illustration of this. Antihypertensive treatment resistance affects an additional 5 million people and is defined as the inability to regulate BP despite the use of at least three antihypertensive drugs in combination.3

Increasing age, racial variables, history in household members, obese status, physical inactivity, larger amounts of salt consumption, stress, tobacco use, and heavy alcohol use are some of the potential etiological factors for essential hypertension.4 It has been examined in previous meta-analyses how vitamin D supplementation affects BP,5 but it is still unclear whether this connection is causal in the general population. This study focused on finding out the effect of vitamin D3 deficiency on BP.

Vitamin D, a steroid hormone, promotes the calcium and phosphate absorption from the gastro-intestinal tract (GIT) and reabsorption from the renal tubules. At low levels, it causes bone mineralization. At high doses, it causes bone resorption. It contributes significantly to mineral metabolism and skeletal homeostasis in this way.3

Up to 80% of human vitamin D comes from vitamin D3, which is produced in the skin by ultraviolet (UV) radiation from 7-dehydrocholesterol. Fish, egg yolk, fortified milk, cereal, juice, and yogurt are dietary sources of vitamin D that provide D2 as well as D3 forms and account for around 20% of the body's requirement. The significant vitamin D form, 25-hydroxyvitamin D [25(OH)D], is produced by the liver from D2 and D3 forms of vitamin D in the body. It is the most accurate measure of the action status and levels of vitamin D. It mostly depends on the serum vitamin D binding protein.4

According to the Institution of Endocrinology clinical practice guidelines, blood 25-hydroxyvitamin D [25(OH)D] results below 20 ng/mL (or 50 nmol/L) are considered deficient levels of vitamin D. Inadequate vitamin D status is ubiquitous among Chinese.4 Numerous studies have been published describing how vitamin D deficiency can lead to cancer,6-10 metabolic disorders, and cardiovascular disease. It has been shown to be negatively correlated with risk. It has been hypothesized that fluctuations in BP may be related to vitamin D administration among individuals with deficient levels of vitamin D.11 Regular vitamin D provision can lower levels of blood-pressure in patients with low levels of vitamin D, without the need for high doses of medication. It may be a simple cure for what can become a chronic condition.12

Every 10% rise in 25-hydroxyvitamin D concentration was found to result in an 8.1% reduction in the risk of hypertension.13 Researchers are considering further research into how Vitamin D deficiency may affect other risk factors for heart disease, such as the likelihood of Type 2 diabetes and high cholesterol, after discovering this potentially significant association.

To date, over several randomized clinical trials have been organized by researchers to determine whether vitamin D administration lowers BP and determine its role as a prevention strategy.14-16 The results of these studies are mixed, as they demonstrate an unsatisfactory design, and the mechanisms underlying how vitamin D affects hypertension remain to be deciphered. Therefore, many meta-analytical studies have attempted to integrate previous results and thereby assess the functional relation of vitamin D administration in regulating BP.4

A meta analysis published earlier by Zhang et al.15 has found that the risk of hypertension was significantly increased when 25(OH)D was reduced below 75 nmol/L, but continued to be prominent in the 75–130 nmol/L range. BP is approximately L-shaped (nonlinearity = 0.04). However, aggregated data showed that neither systolic nor diastolic BP was significantly reduced after the vitamin D intervention.

Primary hypertension is caused by many factors that interact with aging by means of hereditary and ecological determinants. Although vitamin D deficit promotes increased vascular tone,16 it may not be a significant environmental factor in regulating normal BP homeostasis, but it does impair the causation of primary HTN among susceptible adult individuals, which works as a catalyst.16, 17 Other noteworthy hypotheses have indicated that vitamin D alters vascular endothelial function or VSM intracellular calcium concentrations. This is the most notable mechanism linking vitamin D to hypertension.18 The enhanced renin-angiotensin-aldosterone system (RAAS) activity and improvement in hypertension observed in studies with vitamin D receptor (VDR) knockout mice point to a critical role for vitamin D as a potential antihypertensive medication.19

Studies conducted previously have been shown to bring inconsistent results. The information presented in this context gives a conclusion accordingly in a cohort of vitamin D-deficient hypertensive patients, moderately high doses containing vitamin D will either restore or close to physiological blood 25(OH)D levels and prominently decrease BP. Surprisingly, some studies failed to observe an improving effect of vitamin D on BP. However, the contradicting results may be due to poor research methods, confounding role of other anti-hypertensive agents, and <10 cohorts. Forty percent of people have vitamin D deficiency along with having either extremely low or increased levels of intaking vitamin D. In normotensive subjects with or without vitamin D, there was little effect on BP.17

However, from a 5-year VITAL experiment, supplementing a cohort of people at ages likely to develop vitamin D deficiency levels with high regular amounts of intake of vitamin D reduced hypertension, which may be circumvented. This VITAL study has also found a reduction in cancer-related risks, apart from reducing hypertension.12

Advances in clinical research coupled with detailed mechanistic studies may pave the way for large-scale clinical trials conducted in specific demographic groups. The public health burden of managing PH is reduced when vitamin D supplements are administered to the population, reducing the public health burden and helping to dramatically improve clinical practice of PH interventions. Physicians are also encouraged to check their patients' vitamin D levels to help control increasingly frequent high BP.

Naga P. Vakkalagadda: Conceptualization; manuscript writing and editing. Sri H. Narayana: Conceptualization; manuscript writing and editing. Gummadi S. Sree: Manuscript writing and editing. Lakshmi D. Bethineedi: Manuscript writing and editing. L. V. Simhachalam Kutikuppala: Manuscript writing and editing; submission. Gnana D. Medarametla: Manuscript editing.

The authors declare no conflict of interest.

None.

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来源期刊
CiteScore
6.70
自引率
0.00%
发文量
195
审稿时长
35 weeks
期刊介绍: This journal aims to promote progress from basic research to clinical practice and to provide a forum for communication among basic, translational, and clinical research practitioners and physicians from all relevant disciplines. Chronic diseases such as cardiovascular diseases, cancer, diabetes, stroke, chronic respiratory diseases (such as asthma and COPD), chronic kidney diseases, and related translational research. Topics of interest for Chronic Diseases and Translational Medicine include Research and commentary on models of chronic diseases with significant implications for disease diagnosis and treatment Investigative studies of human biology with an emphasis on disease Perspectives and reviews on research topics that discuss the implications of findings from the viewpoints of basic science and clinical practic.
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Table of Contents Guide for Authors Association of cardiorenal biomarkers with mortality in metabolic syndrome patients: A prospective cohort study from NHANES Current status and perspectives in environmental oncology S-acylation of Ca2+ transport proteins in cancer
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