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. 2024 Feb 20;13(4):e030427.
doi: 10.1161/JAHA.123.030427. Epub 2024 Feb 13.

Effect of Accessory Renal Arteries on Essential Hypertension and Related Mechanisms

Affiliations

Effect of Accessory Renal Arteries on Essential Hypertension and Related Mechanisms

Fengyuan Wu et al. J Am Heart Assoc. .

Abstract

Background: This case-control study aimed to determine whether there were differences between patients with essential hypertension with accessory renal arteries (ARAs) and those without ARAs.

Methods and results: The enrolled patients with essential hypertension were divided into the ARA group (n=200) and control group without ARAs (n=238). After propensity matching, 394 patients (197 in each of the 2 groups), were included. The 24-hour BP (4.33/2.43 mm Hg) and daytime BP (4.48/2.61 mm Hg) of patients in the ARA group were significantly higher than those of the control group (P<0.05). The flow-mediated dilation was lower in the ARA group (5.98±2.70 versus 5.18±2.66; P<0.05). In correlation analysis, the horizontal plasma aldosterone concentration had the highest correlation with 24-hour, daytime, and nighttime systolic BP (r=0.263, 0.247, and 0.243, respectively; P<0.05) and diastolic BP (r=0.325, 0.298, and 0.317, respectively; P<0.05). As for multivariate regression analysis, plasma aldosterone concentration was a significant risk factor for elevated 24-hour, daytime, and nighttime systolic BP (β=0.249 [95% CI, 0.150-0.349], 0.228 [95% CI, 0.128-0.329], and 0.282 [95% CI, 0.187-0.377], respectively; P<0.05) and elevated diastolic BP (β=0.289 [95% CI, 0.192-0.385], 0.256 [95% CI, 0.158-0.353], and 0.335 [95% CI, 0.243-0.427], respectively; P<0.05). Direct renin concentration was also a risk factor for 24-hour and daytime BPs, whereas heart rate was a risk factor correlated with 24-hour, daytime, and nighttime diastolic BP (all P<0.05). For the mixed-effects model for repeated measures, the results were similar to results of the multivariate regression analysis (all P<0.05).

Conclusions: ARAs could contribute a higher BP of patients with essential hypertension and might promote the development of essential hypertension. The mechanism might be related to overactivation of the renin-angiotensin-aldosterone system and sympathetic nervous system.

Keywords: accessory renal artery; aldosterone; essential hypertension; renin; sympathetic nervous activity.

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Figures

Figure 1
Figure 1. Flowchart of the study.
AMI indicates acute myocardial infarction; ARA, accessory renal artery; CTA, computed tomography angiography; DRC, direct renin concentration; HF, heart failure; LVEF, left ventricular ejection fraction; and PAC, plasma aldosterone concentration.
Figure 2
Figure 2. Comparison of ambulatory blood pressure (BP) monitoring.
A, Systolic BP (SBP) in the control group and accessory renal artery (ARA) group. B, Diastolic BP (DBP) in the control group and ARA group.
Figure 3
Figure 3. Comparison of the renin‐angiotensin‐aldosterone system and sympathetic nervous system.
A, Direct renin concentration (DRC) in the control group and accessory renal artery (ARA) group. B, Angiotensin II (Ang II) in the control group and ARA group. C, Plasma aldosterone concentration (PAC) in the control group and ARA group. D, Norepinephrine (NE) in the control group and ARA group. E, Heart rate (HR) in the control group and ARA group.

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