Literature DB >> 18049024

Renoprotective effect of the addition of losartan to ongoing treatment with an angiotensin converting enzyme inhibitor in type-2 diabetic patients with nephropathy.

Hirohiko Abe1, Shinya Minatoguchi, Hiroshige Ohashi, Ichijiro Murata, Taro Minagawa, Toshio Okuma, Hitomi Yokoyama, Hisato Takatsu, Tadatake Takaya, Toshihiko Nagano, Yukio Osumi, Masao Kakami, Tatsuo Tsukamoto, Tsutomu Tanaka, Kunihiko Hiei, Hisayoshi Fujiwara.   

Abstract

Angiotensin converting enzyme inhibitors (ACE-Is) and angiotensin II receptor blockers (ARBs) are frequently used for the treatment for glomerulonephritis and diabetic nephropathy because of their albuminuria- or proteinuria-reducing effects. To many patients who are nonresponsive to monotherapy with these agents, combination therapy appears to be a good treatment option. In the present study, we examined the effects of the addition of an ARB (losartan) followed by titration upon addition and at 3 and 6 months (n=14) and the addition of an ACE-I followed by titration upon addition and at 3 and 6 months (n=20) to the drug regimen treatment protocol in type 2 diabetic patients with nephropathy for whom more than 3-month administration of an ACE-I or the combination of an ACE-I plus a conventional antihypertensive was ineffective to achieve a blood pressure (BP) of 130/80 mmHg and to reduce urinary albumin to <30 mg/day. During the 12-month treatment, addition of losartan or addition of an ACE-I to the treatment protocol reduced systolic blood pressure (SBP) by 10% and 12%, diastolic blood pressure (DBP) by 7% and 4%, and urinary albumin excretion by 38% and 20% of the baseline value, respectively. However, the effects on both BP and urinary albumin were not significantly different between the two therapies. In conclusion, addition of losartan or an ACE-I to an ongoing treatment with an ACE-I, or addition of an ACE-I to ongoing treatment with a conventional antihypertensive were equally effective at reducing the urinary albumin excretion and BP, and provided renal protection in patients with type-2 diabetic nephropathy.

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Year:  2007        PMID: 18049024     DOI: 10.1291/hypres.30.929

Source DB:  PubMed          Journal:  Hypertens Res        ISSN: 0916-9636            Impact factor:   3.872


  6 in total

Review 1.  Combination use of angiotensin converting enzyme inhibitors and angiotensin receptor blockers in diabetic kidney disease.

Authors:  Robert C Stanton
Journal:  Curr Diab Rep       Date:  2013-08       Impact factor: 4.810

2.  Efficacy and safety of dual vs single renin-angiotensin-aldosterone system blockade in chronic kidney disease: An updated meta-analysis of randomized controlled trials.

Authors:  Mingming Zhao; Hua Qu; Rumeng Wang; Yi Yu; Meiying Chang; Sijia Ma; Hanwen Zhang; Yuejun Wang; Yu Zhang
Journal:  Medicine (Baltimore)       Date:  2021-09-03       Impact factor: 1.817

3.  Direct evidence for intrarenal chymase-dependent angiotensin II formation on the diabetic renal microvasculature.

Authors:  Sungmi Park; Benjamin J Bivona; Stephen M Ford; Sen Xu; Hiroyuki Kobori; Lawrence de Garavilla; Lisa M Harrison-Bernard
Journal:  Hypertension       Date:  2012-12-03       Impact factor: 10.190

4.  Major role for ACE-independent intrarenal ANG II formation in type II diabetes.

Authors:  Sungmi Park; Benjamin J Bivona; Hiroyuki Kobori; Dale M Seth; Mark C Chappell; Eric Lazartigues; Lisa M Harrison-Bernard
Journal:  Am J Physiol Renal Physiol       Date:  2009-10-21

Review 5.  Dual blockade of the renin-angiotensin system in diabetic nephropathy.

Authors:  Mordchai Ravid
Journal:  Diabetes Care       Date:  2009-11       Impact factor: 19.112

6.  Comparative efficacy and safety of oral or transdermal opioids in the treatment of knee or hip osteoarthritis: a systematic review and Bayesian network meta-analysis protocol.

Authors:  Jun Wang; Yin Wang; Hui Zhang; Ming Lu; Weilu Gao; Li Yin; Zongsheng Yin
Journal:  BMJ Open       Date:  2018-10-18       Impact factor: 2.692

  6 in total

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