Evidence map›Paper›PMID 27193436›Full record

SynthesisInternational urology and nephrology2016

Effects of mineralocorticoid receptor antagonists on left ventricular mass in chronic kidney disease patients: a systematic review and meta-analysis.

RenJie Lu, Yan Zhang, Xishan Zhu, Zhengda Fan, Shanmei Zhu, Manman Cui, Yanping Zhang, Fenglei Tang

Abstract readMeta-AnalysisSystematic Review
PubMed Publisher
In one paragraph

Synthesis in International urology and nephrology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

RenJie LuDepartment of Pharmacy, The Third People's Hospital of Changzhou, Changzhou, Jiangsu, People's Republic of China.
Yan ZhangDepartment of Internal Medicine, The Third People's Hospital of Changzhou, Changzhou, Jiangsu, People's Republic of China.
Xishan ZhuDepartment of Urinary Surgery, The Third People's Hospital of Changzhou, Changzhou, Jiangsu, People's Republic of China.
Zhengda FanDepartment of Pharmacy, The Third People's Hospital of Changzhou, Changzhou, Jiangsu, People's Republic of China.
Shanmei ZhuDepartment of Pharmacy, The Third People's Hospital of Changzhou, Changzhou, Jiangsu, People's Republic of China.
Manman CuiDepartment of Infectious Diseases, The Third People's Hospital of Changzhou, Changzhou, Jiangsu, People's Republic of China.
Yanping ZhangDepartment of Infectious Diseases, The Third People's Hospital of Changzhou, Changzhou, Jiangsu, People's Republic of China.
Fenglei TangDepartment of Pharmacy, The Third People's Hospital of Changzhou, Changzhou, Jiangsu, People's Republic of China. yyyy20152015@126.com.
Changzhou Third People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMineralocorticoid receptor antagonists (MRAs) are used widely in treatment of heart failure, but their effects on cardiovascular complications and mortality of chronic kidney disease (CKD) are not well known. Thus, we aim to assess such therapeutic effects of MRAs on CKD.

methodsElectronic literature published in any language until Dec 31, 2015, was systematically searched on PubMed, Embase, and Cochrane Central Register of Controlled Trials. Primary outcome was left ventricular mass (LVM) or LVM index (LVMI), and secondary outcome was all-cause mortality and major adverse cardiovascular events (MACEs). Results of continuous outcomes were pooled using mean difference (MD) and standard mean difference (SMD). Risk ratios (RRs) with 95 % confidence intervals (CIs) were pooled using a random- or fixed-effects model.

resultsTotally 12 studies (6 randomized controlled trials with 1003 participants) involving 4935 patients were included. MRA treatment versus non-MRA treatment resulted in a significant change of 0.93 SMD (standard mean difference) in LVM (LVMI), a significant reduction of 22 % in all-cause mortality, a significant reduction of incidence of MACEs (RR 0.65, P = 0.001), significantly higher prevalence rates of hyperkalemia (>5.5 mmol/L), but no significant change in prevalence rates of severe hyperkalemia (>6.0 mmol/L).

conclusionMRA benefits CKD patients in terms of LVMI, all-cause mortality, and MACEs with no incidence of severe hyperkalemia. Nevertheless, the real effects of MRAs on cardiovascular events and mortality as well as their safety in CKD patients should be identified by further studies with prospective and large-sample clinical trials.

Indexed as

Cardiovascular DiseasesCause of DeathHeart VentriclesHyperkalemiaHypertrophy, Left VentricularIncidenceMineralocorticoid Receptor AntagonistsOrgan SizePrevalenceProtective FactorsRenal Insufficiency, ChronicRisk FactorsMineralocorticoid Receptor AntagonistsAldosterone receptor antagonistCardiovascular eventsChronic kidney diseaseLeft ventricular massMortality

Identifiers

PMID27193436
OpenAlexW2398725298

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.