TY - JOUR
T1 - Identification of the stages of diabetic nephropathy at which angiotensin II receptor blockers most effectively suppress albuminuria
AU - Ogawa, Susumu
AU - Matsushima, Masato
AU - Mori, Takefumi
AU - Okamura, Masashi
AU - Senda, Miho
AU - Sakamoto, Takuya
AU - Nako, Kazuhiro
AU - Ito, Sadayoshi
N1 - Funding Information:
This work was supported by a 21st Century Center of Excellence Program Special Research Grant from the Ministry of Education, Sports and Culture; a research grant for cardiovascular research (13C-5) from the Japanese Ministry of Health, Labor and Welfare; Longitudinal/Cross-Sectional Studies to Generate Evidence for the Diagnosis/ Management of Metabolic Syndrome for Health Guidance; and Longitudinal/Cross-Sectional Studies to Generate Evidence for Diagnosis/Management of Metabolic Syndrome in Governmental Health Check-up and Guidance System.
PY - 2013/9
Y1 - 2013/9
N2 - BACKGROUNDIt is unclear when angiotensin II receptor blockers (ARBs) produce their strongest antialbuminuric effect (AAE) in patients with diabetic nephropathy. ARBs produce stronger AAEs when urinary excretion of reactive oxygen species (ROS) and/or of angiotensinogen (AGT) is higher before treatment, although the relationship between ROS, AGT, and the urinary albumin-to-creatinine ratio (ACR) is unclear. We sought to define the relationship between ROS and ACR and establish the stage at which ARBs exert maximal AAEs.METHODSUrinary ROS and AGT and the ACR were measured in 277 hypertensive type 2 diabetic patients before ARB treatment, and changes in the ACR were analyzed over16 weeks.RESULTSUrinary AGT and ROS showed similar changes as the disease progressed, and the increase in ACR often observed in patients with lower ROS and AGT reflects the mild AAE produced by ARBs. ROS and AGT levels and the AAE were all highest in albuminuric patients (ACR = 30-1,000mg/g creatinine), whereas normoalbuminuric patients (ACR < 30mg/g creatinine) displayed variable ROS values and AAEs. Glycemic control exerted a stronger AAE than ARBs in normoalbuminuric patients, whereas it had a weak AAE in most nephrotic (ACR ≥ 1,000mg/g creatinine) patients, who had low basal ROS and AGT values. Lowering blood pressure was effective at all stages and appeared to promote an AAE, even in nephrotic patients.CONCLUSIONSARBs produce a maximal AAE in albuminuric patients, and lowering blood pressure enhances the AAE in patients at all stages, including the nephrotic stage.
AB - BACKGROUNDIt is unclear when angiotensin II receptor blockers (ARBs) produce their strongest antialbuminuric effect (AAE) in patients with diabetic nephropathy. ARBs produce stronger AAEs when urinary excretion of reactive oxygen species (ROS) and/or of angiotensinogen (AGT) is higher before treatment, although the relationship between ROS, AGT, and the urinary albumin-to-creatinine ratio (ACR) is unclear. We sought to define the relationship between ROS and ACR and establish the stage at which ARBs exert maximal AAEs.METHODSUrinary ROS and AGT and the ACR were measured in 277 hypertensive type 2 diabetic patients before ARB treatment, and changes in the ACR were analyzed over16 weeks.RESULTSUrinary AGT and ROS showed similar changes as the disease progressed, and the increase in ACR often observed in patients with lower ROS and AGT reflects the mild AAE produced by ARBs. ROS and AGT levels and the AAE were all highest in albuminuric patients (ACR = 30-1,000mg/g creatinine), whereas normoalbuminuric patients (ACR < 30mg/g creatinine) displayed variable ROS values and AAEs. Glycemic control exerted a stronger AAE than ARBs in normoalbuminuric patients, whereas it had a weak AAE in most nephrotic (ACR ≥ 1,000mg/g creatinine) patients, who had low basal ROS and AGT values. Lowering blood pressure was effective at all stages and appeared to promote an AAE, even in nephrotic patients.CONCLUSIONSARBs produce a maximal AAE in albuminuric patients, and lowering blood pressure enhances the AAE in patients at all stages, including the nephrotic stage.
KW - albuminuria
KW - angiotensin II receptor blockers
KW - angiotensinogen
KW - blood pressure
KW - diabetic nephropathy
KW - hypertension
KW - oxidative stress.
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U2 - 10.1093/ajh/hpt085
DO - 10.1093/ajh/hpt085
M3 - Article
C2 - 23775091
AN - SCOPUS:84882299067
SN - 0895-7061
VL - 26
SP - 1064
EP - 1069
JO - American Journal of Hypertension
JF - American Journal of Hypertension
IS - 9
ER -