Morishita Yoshiyuki, Yasui Toshihiro, Numata Akihiko, Onishi Akira, Ishibashi Kenichi, Kusano Eiji
Department of Internal Medicine, Jichi Medical University, Shimotsuke, Japan;
Int J Nephrol Renovasc Dis. 2012;5:125-33. doi: 10.2147/IJNRD.S36451. Epub 2012 Sep 21.
We investigated the effects of aliskiren in terms of its inhibition of the renin-angiotensin-aldosterone system (RAAS) as well as that on blood pressure (BP), and renal and cardiac protection in elderly chronic kidney disease (CKD) patients with hypertension.
Nineteen elderly CKD patients (nine males, ten females, aged 74.6 ± 5.8 years) were assigned to receive 150 mg/day of aliskiren added to existing antihypertensives for 6 months. Changes in plasma renin activity (PRA), angiotensin I (Ang I), angiotensin II (Ang II), aldosterone (Ald), BP, estimated glomerular filtration rate (eGFR), urine albumin/creatinine ratio (UACR), left ventricular ejection fraction (LVEF), interventricular septum thickness (IVST), left ventricular posterior wall thickness (LVPWT), and plasma brain natriuretic peptide (BNP) levels were evaluated.
ALISKIREN SUPPRESSED THE RAAS AS FOLLOWS: PRA 1.3 ± 1.0 to 0.3 ± 0.3 ng/mL/hour, P < 0.05; Ang I 59.5 ± 32.1 to 26.0 ± 17.3 pg/mL, P < 0.05; Ang II 58.4 ± 62.1 to 14.3 ± 9.0 pg/mL, P < 0.05; and Ald 86.1 ± 38.3 to 80.1 ± 52.6 pg/mL, not significant (NS). Aliskiren reduced BP (153.6/77.2 ± 14.9/10.4 to 130.9/72.2 ± 15.6/9.9 mmHg, P < 0.05). It also reduced UACR (747.1 ± 1121.4 to 409.6 ± 636.8 mg/g, P < 0.05), whereas it did not change eGFR (52.1 ± 29.2 to 51.2 ± 29.3 mL/min/1.73 m(2), NS), LVEF (66.8 ± 7.9 to 66.5% ± 6.8%, NS), IVST (10.1 ± 1.8 to 9.9 ± 1.8 mm, NS), LVPWT (10.0 ± 1.6 mm to 10.0 ± 1.4 mm, NS), or BNP (48.2 ± 46.0 to 54.9 ± 41.1 pg/mL, NS).
Aliskiren was effective for BP control and reduced UACR while maintaining eGFR and heart function in elderly CKD patients with hypertension.
我们研究了阿利吉仑在抑制肾素 - 血管紧张素 - 醛固酮系统(RAAS)方面的作用,以及对老年慢性肾脏病(CKD)合并高血压患者血压(BP)、肾脏和心脏保护的影响。
19例老年CKD患者(9例男性,10例女性,年龄74.6±5.8岁)被分配接受在现有降压药基础上加用150mg/天阿利吉仑,疗程6个月。评估血浆肾素活性(PRA)、血管紧张素I(Ang I)、血管紧张素II(Ang II)、醛固酮(Ald)、血压、估计肾小球滤过率(eGFR)、尿白蛋白/肌酐比值(UACR)、左心室射血分数(LVEF)、室间隔厚度(IVST)、左心室后壁厚度(LVPWT)和血浆脑钠肽(BNP)水平的变化。
阿利吉仑对RAAS的抑制作用如下:PRA从1.3±1.0降至0.3±0.3ng/mL/小时,P<0.05;Ang I从59.5±32.1降至26.0±17.3pg/mL,P<0.05;Ang II从58.4±62.1降至14.3±9.0pg/mL,P<0.05;Ald从86.1±38.3降至80.1±52.6pg/mL,差异无统计学意义(NS)。阿利吉仑降低了血压(从153.6/77.2±14.9/10.4降至130.9/72.2±15.6/9.9mmHg,P<0.05)。它还降低了UACR(从747.1±1121.4降至409.6±636.8mg/g,P<0.05),而eGFR(从52.1±29.2降至至51.2±29.3mL/min/1.73m²,NS)、LVEF(从66.8±7.9降至66.5%±6.8%,NS)、IVST(从10.