浏览全部资源
扫码关注微信
衡水市人民医院肾内科,河北 衡水 053000
主治医师,硕士。研究方向:高血压肾损害、药物降压降脂。E-mail:yuanyucong2003@163.com
纸质出版日期:2023-07-15,
收稿日期:2023-02-10,
修回日期:2023-04-25,
扫 描 看 全 文
苑玉聪,张瑞英,王红等.阿法骨化醇对高血压肾损害患者肝肾功能、炎症因子及RAS活性的影响 Δ[J].中国药房,2023,34(13):1617-1621.
YUAN Yucong,ZHANG Ruiying,WANG Hong,et al.Efficacy of alfacalcidol on liver and kidney function, inflammatory cytokines and RAS activity in hypertensive patients with renal impairment[J].ZHONGGUO YAOFANG,2023,34(13):1617-1621.
苑玉聪,张瑞英,王红等.阿法骨化醇对高血压肾损害患者肝肾功能、炎症因子及RAS活性的影响 Δ[J].中国药房,2023,34(13):1617-1621. DOI: 10.6039/j.issn.1001-0408.2023.13.14.
YUAN Yucong,ZHANG Ruiying,WANG Hong,et al.Efficacy of alfacalcidol on liver and kidney function, inflammatory cytokines and RAS activity in hypertensive patients with renal impairment[J].ZHONGGUO YAOFANG,2023,34(13):1617-1621. DOI: 10.6039/j.issn.1001-0408.2023.13.14.
目的
2
探讨阿法骨化醇联合常规降压降脂药对高血压肾损害患者肝肾功能、血清炎症因子与肾素-血管紧张素系统(RAS)活性的影响。
方法
2
选择2017年12月-2020年12月在我院肾内科就诊的高血压肾损害患者200例,按随机数表法分为对照组和观察组,每组100例。2组患者均给予常规降压降脂治疗(共14周),观察组患者在治疗2周后联合给予口服阿法骨化醇治疗(每次0.25 μg,每日1次,共12周)。观察2组患者治疗前后的肝功能指标[天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)]、肾功能指标[血钙、血磷、尿素氮(BUN)、胱抑素C(Cys-C)、血清肌酐(Scr)、尿微量白蛋白(mAlb)、β
2
微球蛋白(β
2
-MG)、尿
N
-乙酰
β
-D-氨基葡萄糖苷酶(NAG)、24 h尿蛋白水平]、炎症因子[血清白细胞介素6(IL-6)、肿瘤坏死因子α(TNF-α)、高敏C-反应蛋白(hs-CRP)]
水平、RAS活性指标[血清肾素、血管紧张素Ⅰ(Ang Ⅰ)、Ang Ⅱ、醛固酮]水平,并记录治疗期间不良反应发生情况。
结果
2
2组患者在治疗前的各项检测指标水平比较,差异均无统计学意义(
P
>0.05)。治疗后,观察组患者的血钙水平较治疗前显著升高(
P
<0.05),但仍维持在临床正常水平;观察组患者的Cys-C、Scr、BUN、尿mAlb、β
2
-MG、NAG、24 h尿蛋白水平、hs-CRP、IL-6、TNF-α、血清肾素、Ang Ⅰ、Ang Ⅱ和醛固酮水平较治疗前显著下降(
P
<0.05)。治疗后,观察组患者的血钙水平显著高于对照组(
P
<0.05);而Cys-C、Scr、BUN、尿mAlb、β
2
-MG、NAG、24 h尿蛋白水平、hs-CRP、IL-6、TNF-α、血清肾素、Ang Ⅰ、Ang Ⅱ和醛固酮水平显著低于对照组(
P
<0.05)。2组患者用药期间不良反应发生率比较,差异无统计学意义(
P
>0.05)。
结论
2
在常规降压降脂药基础上联用阿法骨化醇能有效改善高血压肾损害患者肝肾功能,抑制其炎症反应和RAS活性,且安全性良好。
OBJECTIVE
2
To explore the efficacy of alfacalcidol combined with conventional antihypertensive and lipid-lowering drugs on liver and kidney function, serum inflammatory cytokines and renin-angiotensin system(RAS) in hypertensive patients with renal impairment.
METHODS
2
A total of 200 hypertensive patients with renal impairment who were treated in the department of nephrology in our hospital from December 2017 to December 2020 were selected and randomly divided into control group and observation group, with 100 cases in each group. Both groups of patients were treated with conventional antihypertensive and lipid-lowering drugs for a total of 14 weeks, patients in the observation group were additionally treated with oral alfacalcidol after 2 weeks of treatment (0.25 μg each time, once a day, for a total of 12 weeks). The levels of liver function indexes [aspartate aminotransferase (AST), alanine aminotransferase (ALT)], renal function indexes [blood calcium, blood phosphorus, blood urea nitrogen (BUN), cystatin C (Cys-C), serum creatinine (Scr), urine microalbumin (mAlb), β
2
-microglobulin (β
2
-MG), urinary
N
-acetyl
β
-D-glucosaminidase (NAG), 24 h urinary protein], inflammatory factors [serum interleukin 6 (IL-6), tumor necrosis factor α (TNF-α), hypersensitive C-reactive protein (hs-CRP)]
and RAS activity indexes [renin, angiotensin Ⅰ(Ang Ⅰ), Ang Ⅱ and aldosterone] were observed in 2 groups before and after treatment, and the occurrence of adverse drug reactions was recorded during treatment.
RESULTS
2
There was no statistical significance in the levels of detection indexes between 2 groups before treatment (
P
>0.05). After treatment, the level of blood calcium in the observation group was significantly higher than before treatment (
P
<0.05), but remained at clinically normal level. Compared with before treatment, the levels of Cys-C, Scr, BUN, urine mAlb, β
2
-MG, NAG and 24 h urinary protein, hs-CRP, IL-6, TNF-α, renin, Ang Ⅰ, Ang Ⅱ and aldosterone were significantly decreased in the observation group after treatment (
P
<0.05). After treatment, the level of blood calcium in observation group was significantly higher than control group (
P
<0.05). Additionally, the levels of Cys-C, Scr, BUN, urine mAlb, β
2
-MG, NAG, 24 h urinary protein, hs-CRP, IL-6, TNF-α, renin, Ang Ⅰ, Ang Ⅱ and aldosterone were significantly lower than control group (
P
<0.05). There was no statistical significance in the incidence of adverse drug reactions between 2 groups during treatment (
P
>0.05).
CONCLUSIONS
2
Alfacalcidol combined with routine therapy of antihypertensive and lipid-lowering drugs could effectively improve liver and renal functions, inhibit inflammation and RAS activity in hypertensive patients with renal impairment, with a favorable safety.
阿法骨化醇高血压肾损害肾素-血管紧张素系统炎症因子
hypertensive renal impairmentrenin-angiotensin systeminflammatory cytokines
《中国心血管健康与疾病报告》编写组.《中国心血管健康与疾病报告2021》概述[J]. 中国心血管病研究,2022,20(7):577-596.
SUN D,WANG J J,SHAO W S,et al. Pathogenesis and damage targets of hypertensive kidney injury[J]. J Transl Int Med,2020,8(4):205-209.
SHARMA N,ANDERS H J,GAIKWAD A B. Fiend and friend in the renin angiotensin system:an insight on acute kidney injury[J]. Biomed Pharmacother,2019,110:764-774.
徐嘉欣,殷立平. 炎症在高血压肾损害中的研究进展[J]. 中国处方药,2022,20(4):189-191.
张小丽,王旭桃,徐文俭. 阿法骨化醇联合缬沙坦治疗糖尿病肾病的临床研究[J]. 实用糖尿病杂志,2020,16(6):39.
李六生,闫志群,周志华,等. 不同剂量阿法骨化醇对IgA肾病患者血清TNF-α、IL-6、TGF-β1水平的影响[J]. 广东医学,2016,37(7):1067-1070.
王红,苑玉聪,张瑞英,等. 高血压肾损害应用不同剂量阿法骨化醇治疗的临床疗效和安全性[J]. 中国老年学杂志,2020,40(18):3898-3901.
National Kidney Foundation. K/DOQI clinical practice guidelines for chronic kidney disease:evaluation,classification,and stratification[J]. Am J Kidney Dis,2002,39(2 Suppl 1):S1-S266.
钟方明,高艳香,郑金刚. 高血压肾损害发病机制的研究进展[J]. 中日友好医院学报,2015,29(6):364-366.
PUSHPAKUMAR S,REN L,JUIN S K,et al. Methylation-dependent antioxidant-redox imbalance regulates hypertensive kidney injury in aging[J]. Redox Biol,2020,37:101754.
YE Z F,LIU H,ZHAO B X,et al. Correlation and diagnostic value of serum Cys-C,RBP4,and NGAL with the condition of patients with traumatic acute kidney injury[J]. Evid Based Complement Alternat Med,2021,2021:4990941.
王芳,谢敏妍,张东升,等. 阿法骨化醇冲击治疗对维持性血液透析患者钙磷代谢、微炎症及氧化应激状态的影响[J]. 实用药物与临床,2018,21(7):765-768.
袁俊蓉. 胱抑素C、肌酐和尿素氮在肾脏损害中的诊断价值[J]. 中外医学研究,2017,15(18):47-48.
彭俊华,张全华,赵勇,等. 血清β2-MG,Cys-C及U-mALB在高血压肾损伤中的应用[J]. 现代检验医学杂志,2014,29(4):147-149.
蔡晓婵,汤建新,刘健华,等. 血肌酐值在慢性肾病肾功能评价中的临床应用[J]. 中国医药指南,2011,9(18):78-79.
赵卫红,陈小华,黄曾,等. 血清胱抑素 C 对肾脏早期损伤评价的临床意义[J]. 现代诊断与治疗,2013,24(18):4093-4094.
成守金,罗云杰,许贺春. 尿液mALB、β2-MG、NAG联合检测对高血压病早期肾损伤的诊断价值[J]. 中国临床研究,2012,25(5):489-491.
WEN Y,CROWLEY S D. Renal effects of cytokines in hypertension[J].Curr Opin Nephrol Hypertens,2018,27(2):70-76.
林武荣. 血清hs-CRP、IL-6、IL-18在高血压肾损害患者中变化的意义[J]. 中外医疗,2012,31(17):12,14.
张凤,戴小华. IL-6、TNF-α参与高血压肾损害研究进展[J]. 中医药临床杂志,2014,26(1):78-80.
DAS U N. Renin-angiotensin-aldosterone system in insulin resistance and metabolic syndrome[J]. J Transl Int Med,2016,4(2):66-72.
DOLEŽELOVÁ Š,JÍCHOVÁ Š,HUSKOVÁ Z,et al. Progression of hypertension and kidney disease in aging fawn-hooded rats is mediated by enhanced influence of renin-angiotensin system and suppression of nitric oxide system and epoxyeicosanoids[J]. Clin Exp Hypertens,2016,38(7):644-651.
BHANDARI S,MEHTA S,KHWAJA A,et al. Renin-angiotensin system inhibition in advanced chronic kidney disease[J]. N Engl J Med,2022,387(22):2021-2032.
ISHIGAKI S,OHASHI N,ISOBE S,et al. Impaired endogenous nighttime melatonin secretion relates to intrarenal renin-angiotensin system activation and renal damage in patients with chronic kidney disease[J]. Clin Exp Nephrol,2016,20(6):878-884.
0
浏览量
3
下载量
0
CSCD
关联资源
相关文章
相关作者
相关机构