全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

沙库巴曲缬沙坦对老年高血压患者降压疗效及炎症因子影响
Effect of Sacubitril-Valsartan on Antihypertensive Efficacy Inflammatory Factors in Elderly Patients with Hyperten-sion

DOI: 10.12677/ACM.2023.133583, PP. 4063-4071

Keywords: 沙库巴曲缬沙坦,缬沙坦,原发性高血压,炎症因子
Sacubitril-Valsartan
, Valsartan, Essential Hypertension, Inflammatory Factors

Full-Text   Cite this paper   Add to My Lib

Abstract:

目的:比较沙库巴曲缬沙坦与缬沙坦对老年原发性高血压患者降压疗效及炎症因子水平的影响。方法:回顾性选取2021年7月1日至2022年7月1日在青岛大学附属医院住院的老年原发性高血压患者215例。根据患者服用降压药物不同分为沙库巴曲缬沙坦(200 mg/次 1次/天)组(n = 71)和缬沙坦组(80 mg/次 1次/天) (n = 82)。收集两组患者病历资料,观察患者8周后的诊室血压[平均坐位收缩压(mean sitting Systolic Blood Pressure, msSBP)、平均坐位舒张压(mean sitting Diastolic Blood Pressure, msDBP)]和炎症因子[(白细胞介素-1β (Interleukin 1β, IL-1β)、IL-2、IL-4、IL-5、IL-6、IL-8、IL-10、IL-17、肿瘤坏死因子(Tumor Necrosis Factor, TNF)-α (TNF-α)]差异。结果:沙库巴曲缬沙坦钠组患者治疗8周以后的诊室血压下降幅度和诊室血压达标率较缬沙坦组高(P < 0.05);两组患者治疗8周以后血浆IL-1β、IL-6、IL-10、IL-17、TNF-α的差值组内比较有统计学意义(P < 0.05);沙库巴曲缬沙坦组患者IL-17的下降幅度明显高于缬沙坦组、抑炎因子IL-10的升高幅度明显高于缬沙坦组(P均 < 0.05);余细胞因子(IL-4、IL-6、IL-8、IL-1β、IL-2、IL-5、TNF-α)两组间无明显统计学差异。结论:在原发性高血压的药物治疗中,与缬沙坦相比,沙库巴曲缬沙坦能更好地降低诊室血压,提高诊室血压达标率,其机制可能与降低体内促炎因子(IL-17)水平,提高体内抑炎因子(IL-10)水平有关。
Objective: To compare the effect of sacubitril-valsartan and valsartan on antihypertensive efficacy and inflammatory factor levels in elderly patients with essential hypertension. Methods: A total of 215 elderly patients with essential hypertension who were hospitalized in the Affiliated Hospital of Qingdao University from July 1, 2021 to July 1, 2022 were selected. Patients were divided into sacu-bitril- valsartan (200 mg/qd) group (n = 71) and valsartan (80 mg/qd) group (n = 82) according to the different antihypertensive drugs taken. The medical records of the two groups of patients were collected to observe the difference in clinic’s blood pressure [mean sitting Systolic Blood Pressure (msSBP), mean sitting Diastolic Blood Pressure (msDBP)] and inflammatory factors [Interleukin 1β (IL-1β), IL-2, IL-4, IL-5, IL-6, IL-8, IL-10, IL-17, Tumor Necrosis Factor-α (TNF-α)] after 8 weeks. Re-sults: After 8 weeks of treatment, the decrease in office blood pressure and the rate of meeting the standard of office blood pressure in the sacubitril-valsartan group after 8 weeks of treatment were higher than those in the valsartan group (P < 0.05), the levels of IL-1β, IL-6, IL-10, IL-17 and TNF-α were statistically significant compared with those before treatment (P < 0.05), the decrease of IL-17 in the sacubitril-valsartan group was significantly higher than that in the valsartan group, the in-crease in inflammatory factor IL-10 was significantly higher than that in the valsartan group (P < 0.05). There was no significant difference in the other inflammatory factors (IL-4, IL-6, IL-8, IL-1β, IL-2, IL-5, TNF-α) between the two groups. Conclusion: In the treatment of essential hypertension, sacubitril-valsartan can better reduce office blood pressure and improve office blood pressure com-pliance

References

[1]  Forouzanfar, M.H., Liu, P., Roth, G.A., et al. (2017) Global Burden of Hypertension and Systolic Blood Pressure of at Least 110 to 115 mm Hg, 1990-2015. JAMA, 317, 165-182.
https://doi.org/10.1001/jama.2016.19043
[2]  Mills, K.T., Stefanescu, A. and He, J. (2020) The Global Epidemiology of Hypertension. Nature Reviews Nephrology, 16, 223-237.
https://doi.org/10.1038/s41581-019-0244-2
[3]  Whelton, P.K., Carey, R.M., Aronow, W.S., et al. (2018) 2017 ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ ASPC/NMA/PCNA Guideline for the Prevention, Detection, Evaluation, and Management of High Blood Pressure in Adults: A Report of the American College of Cardiolo-gy/American Heart Association Task Force on Clinical Practice Guidelines. Journal of the American College of Cardiol-ogy, 71, e127-e248.
https://doi.org/10.1161/HYP.0000000000000076
[4]  张跃, 李宁, 邱健, 等. 血管紧张素受体脑啡肽酶抑制剂沙库巴曲缬沙坦治疗高血压的研究进展[J]. 中华高血压杂志, 2021, 29(6): 519-524.
[5]  Agita, A. and Alsagaff, M.T. (2017) Inflammation, Immunity, and Hypertension. Acta Medica Indonesiana, 49, 158-165.
[6]  Idris-Khodja, N., Mian, M.O., Paradis, P., et al. (2014) Dual Opposing Roles of Adaptive Immunity in Hypertension. European Heart Journal, 35, 1238-1244.
https://doi.org/10.1093/eurheartj/ehu119
[7]  中国高血压防治指南(2018年修订版) [J]. 中国心血管杂志, 2019, 24(1): 24-56.
[8]  Iglesias-Garriz, I., Olalla-Gómez, C., Garrote, C., et al. (2012) Contribution of Right Ventricular Dysfunction to Heart Failure Mortality: A Meta-Analysis. Reviews in Cardiovascular Medicine, 13, e62-e69.
https://doi.org/10.3909/ricm0602
[9]  Williams, B., Mancia, G., Spiering, W., et al. (2018) 2018 ESC/ESH Guide-lines for the Management of Arterial Hypertension. European Heart Journal, 39, 3021-3104.
https://doi.org/10.1093/eurheartj/ehy339
[10]  Ettehad, D., Emdin, C.A., Kiran, A., et al. (2016) Blood Pressure Lowering for Prevention of Cardiovascular Disease and Death: A Systematic Review and Meta-Analysis. The Lancet, 387, 957-967.
https://doi.org/10.1016/S0140-6736(15)01225-8
[11]  郑丽, 张续乾, 孙雪林, 等. 沙库巴曲缬沙坦钠治疗高血压有效性和安全性的Meta分析[J]. 中国药物警戒, 2022, 19(10): 1118-1122+1135.
[12]  Bavishi, C., Messerli, F.H., Kadosh, B., et al. (2015) Role of Neprilysin Inhibitor Combinations in Hypertension: Insights from Hypertension and Heart Failure Trials. European Heart Journal, 36, 1967-1973.
https://doi.org/10.1093/eurheartj/ehv142
[13]  Ruilope, L.M., Dukat, A., B?hm, M., et al. (2010) Blood-Pressure Reduction with LCZ696, a Novel Dual-Acting Inhibitor of the Angiotensin II Receptor and Neprilysin: A Randomised, Double-Blind, Placebo-Controlled, Active Comparator Study. The Lancet, 375, 1255-1266.
https://doi.org/10.1016/S0140-6736(09)61966-8
[14]  Kario, K., Sun, N., Chiang, F.T., et al. (2014) Efficacy and Safety of LCZ696, a First-in-Class Angiotensin Receptor Neprilysin Inhibitor, in Asian Patients with Hypertension: A Randomized, Double-Blind, Placebo-Controlled Study. Hypertension (Dallas, Tex: 1979), 63, 698-705.
https://doi.org/10.1161/HYPERTENSIONAHA.113.02002
[15]  Rakugi, H., Kario, K., Yamaguchi, M., et al. (2022) Efficacy of Sacubitril/Valsartan versus Olmesartan in Japanese Patients with Essential Hypertension: A Random-ized, Double-Blind, Multicenter Study. Hypertension Research: Official Journal of the Japanese Society of Hypertension, 45, 824-833.
https://doi.org/10.1038/s41440-021-00819-7
[16]  Kario, K. (2018) The Sacubitril/Valsartan, a First-in-Class, Angiotensin Receptor Neprilysin Inhibitor (ARNI): Potential Uses in Hypertension, Heart Failure, and Beyond. Current Cardiology Reports, 20, 5.
https://doi.org/10.1007/s11886-018-0944-4
[17]  Nielsen, P.M., Grimm, D., Wehland, M., et al. (2018) The Com-bination of Valsartan and Sacubitril in the Treatment of Hypertension and Heart Failure—An Update. Basic & Clinical Pharmacology & Toxicology, 122, 9-18.
https://doi.org/10.1111/bcpt.12912
[18]  D’elia, E., Iacovoni, A., Vaduganathan, M., et al. (2017) Neprilysin Inhibi-tion in Heart Failure: Mechanisms and Substrates beyond Modulating Natriuretic Peptides. European Journal of Heart Failure, 19, 710-717.
https://doi.org/10.1002/ejhf.799
[19]  B?hm, M., Young, R., Jhund, P.S., et al. (2017) Systolic Blood Pressure, Cardiovascular Outcomes and Efficacy and Safety of Sacubitril/Valsartan (LCZ696) in Patients with Chronic Heart Fail-ure and Reduced Ejection Fraction: Results from PARADIGM-HF. European Heart Journal, 38, 1132-1143.
https://doi.org/10.1093/eurheartj/ehw570
[20]  Hubers, S.A. and Brown, N.J. (2016) Combined Angiotensin Re-ceptor Antagonism and Neprilysin Inhibition. Circulation, 133, 1115-1124.
https://doi.org/10.1161/CIRCULATIONAHA.115.018622
[21]  Mcmaster, W.G., Kirabo, A., Madhur, M.S., et al. (2015) Inflammation, Immunity, and Hypertensive End-Organ Damage. Circulation Research, 116, 1022-1033.
https://doi.org/10.1161/CIRCRESAHA.116.303697
[22]  Karbach, S., Croxford, A.L., Oelze, M., et al. (2014) In-terleukin 17 Drives Vascular Inflammation, Endothelial Dysfunction, and Arterial Hypertension in Psoriasis-Like Skin Disease. Arteriosclerosis, Thrombosis, and Vascular Biology, 34, 2658-2668.
https://doi.org/10.1161/ATVBAHA.114.304108
[23]  Nguyen, H., Chiasson, V.L., Chatterjee, P., et al. (2013) In-terleukin-17 Causes Rho-Kinase-Mediated Endothelial Dysfunction and Hypertension. Cardiovascular Research, 97, 696-704.
https://doi.org/10.1093/cvr/cvs422
[24]  Zhou, G., Cheung, A.K., Liu, X., et al. (2014) Valsartan Slows the Progression of Diabetic Nephropathy in db/db Mice via a Reduction in Podocyte Injury, and Renal Oxidative Stress and Inflammation. Clinical Science (London), 126, 707-720.
https://doi.org/10.1042/CS20130223
[25]  Mohany, M., Alanazi, A.Z., Alqahtani, F., et al. (2020) LCZ696 Mitigates Diabetic-Induced Nephropathy through Inhibiting Oxi-dative Stress, NF-κB Mediated Inflammation and Glomerulosclerosis in Rats. PeerJ, 8, e9196.
https://doi.org/10.7717/peerj.9196
[26]  Liang, W., Xie, B.K., Ding, P.W., et al. (2021) Sacubitril/Valsartan Allevi-ates Experimental Autoimmune Myocarditis by Inhibiting Th17 Cell Differentiation Independently of the NLRP3 In-flammasome Pathway. Frontiers in Pharmacology, 12, Article ID: 727838.
https://doi.org/10.3389/fphar.2021.727838

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133