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2016 ; 17
(1
): 127
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Effect of mineralocorticoid receptor antagonists on proteinuria and progression
of chronic kidney disease: a systematic review and meta-analysis
#MMPMID27609359
Currie G
; Taylor AH
; Fujita T
; Ohtsu H
; Lindhardt M
; Rossing P
; Boesby L
; Edwards NC
; Ferro CJ
; Townend JN
; van den Meiracker AH
; Saklayen MG
; Oveisi S
; Jardine AG
; Delles C
; Preiss DJ
; Mark PB
BMC Nephrol
2016[Sep]; 17
(1
): 127
PMID27609359
show ga
BACKGROUND: Hypertension and proteinuria are critically involved in the
progression of chronic kidney disease. Despite treatment with renin angiotensin
system inhibition, kidney function declines in many patients. Aldosterone excess
is a risk factor for progression of kidney disease. Hyperkalaemia is a concern
with the use of mineralocorticoid receptor antagonists. We aimed to determine
whether the renal protective benefits of mineralocorticoid antagonists outweigh
the risk of hyperkalaemia associated with this treatment in patients with chronic
kidney disease. METHODS: We conducted a meta-analysis investigating
renoprotective effects and risk of hyperkalaemia in trials of mineralocorticoid
receptor antagonists in chronic kidney disease. Trials were identified from
MEDLINE (1966-2014), EMBASE (1947-2014) and the Cochrane Clinical Trials
Database. Unpublished summary data were obtained from investigators. We included
randomised controlled trials, and the first period of randomised cross over
trials lasting ?4 weeks in adults. RESULTS: Nineteen trials (21 study groups, 1
646 patients) were included. In random effects meta-analysis, addition of
mineralocorticoid receptor antagonists to renin angiotensin system inhibition
resulted in a reduction from baseline in systolic blood pressure (-5.7 [-9.0,
-2.3] mmHg), diastolic blood pressure (-1.7 [-3.4, -0.1] mmHg) and glomerular
filtration rate (-3.2 [-5.4, -1.0] mL/min/1.73 m(2)). Mineralocorticoid receptor
antagonism reduced weighted mean protein/albumin excretion by 38.7 % but with a
threefold higher relative risk of withdrawing from the trial due to hyperkalaemia
(3.21, [1.19, 8.71]). Death, cardiovascular events and hard renal end points were
not reported in sufficient numbers to analyse. CONCLUSIONS: Mineralocorticoid
receptor antagonism reduces blood pressure and urinary protein/albumin excretion
with a quantifiable risk of hyperkalaemia above predefined study upper limit.
|Angiotensin Receptor Antagonists/therapeutic use
[MESH]
|Angiotensin-Converting Enzyme Inhibitors/therapeutic use
[MESH]
|Blood Pressure/drug effects
[MESH]
|Disease Progression
[MESH]
|Glomerular Filtration Rate/drug effects
[MESH]
|Humans
[MESH]
|Hyperkalemia/*chemically induced
[MESH]
|Mineralocorticoid Receptor Antagonists/adverse effects/*therapeutic use
[MESH]
|Patient Dropouts/statistics & numerical data
[MESH]