Evidence map›Paper›PMID 27377659›Full record

SynthesisJournal of the renin-angiotensin-aldosterone system : JRAAS2016

Protection against death and renal failure by renin-angiotensin system blockers in patients with diabetes and kidney disease.

Jian Shen, Yan-Mei Huang, Xin-Nan Song, Xue-Zhi Hong, Min Wang, Wei Ling, Xiao-Xi Zhang, Hai-Lu Zhao

Open access · hybridAbstract readMeta-AnalysisReview
In one paragraph

Synthesis in Journal of the renin-angiotensin-aldosterone system : JRAAS, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

7 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Hypertension in diabetes.Pediatric nephrology (Berlin, Germany) · 2024
    Article
  4. Diabetic vasculopathy: macro and microvascular injury.Current pathobiology reports · 2020
    Article
  5. Article
  6. Review
  7. Risk for cancer in living kidney donors and recipients.Journal of cancer research and clinical oncology · 2018
    Review
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.

Jian ShenCenter for Diabetic Systems Medicine, Guilin Medical University, China Department of pathology, Affiliated Hospital of Guilin Medical University, China.
Yan-Mei HuangCenter for Diabetic Systems Medicine, Guilin Medical University, China.
Xin-Nan SongDepartment of Anesthetics, Affiliated Hospital of Guilin Medical University, China.
Xue-Zhi HongDepartment of Rheumatology and Immunology, Affiliated Hospital of Guilin Medical University, China.
Min WangCenter for Diabetic Systems Medicine, Guilin Medical University, China.
Wei LingCenter for Diabetic Systems Medicine, Guilin Medical University, China.
Xiao-Xi ZhangCenter for Diabetic Systems Medicine, Guilin Medical University, China.
Hai-Lu ZhaoCenter for Diabetic Systems Medicine, Guilin Medical University, China zhaohailu9@126.com zhaohailu@glmc.edu.cn.
Guilin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAngiotensin-converting enzyme inhibitors (ACEis) and angiotensin receptor blockers (ARBs) are widely used to block the renin-angiotensin system (RAS). Yet it remains uncertain whether these drugs are equally effective and safe.

methodsSystematic reviews and meta-analyses of ACEis/ARBs in diabetes and kidney disease published in PubMed, Chinese National Knowledge Infrastructure (CNKI) and Wanfang databases were searched for clinical outcomes including all-cause mortality, end-stage renal disease (ESRD), hyperkalemia and cough.

resultsEight meta-analyses included 2177-61,264 patients with follow-up of 6-108 months. RAS blockers reduced mortality (relative risk ratio (RR), 0.90, 95% confidence interval (CI), 0.86-0.95) without heterogeneity. The death protection was significant specifically with ACEis (RR, 0.85, 95% CI, 0.79-0.91), but not with ARBs. Protection against ESRD was homogenously evident by ARBs (RR, 0.79, 95% CI, 0.73-0.87), ACEis (RR, 0.79, 95% , 0.64-0.94), and both (RR, 0.79, 95% CI, 0.73-0.87). Significant side effects were hyperkalemia by ARBs (RR, 2.44, 95% CI, 1.13-5.26), and cough by ACEis (RR, 2.38, 95% CI, 1.75-3.22)

conclusionsIn patients with diabetes and kidney disease, ACEis and ARBs are consistently protective for the development of ESRD. Use of ACEis alone additionally reduces deaths and increases the risk for cough. Use of ARBs alone increases the risk for hyperkalemia without additional benefit of death protection.

Indexed as

Renin-Angiotensin SystemAngiotensin-Converting Enzyme InhibitorsAngiotensin II Type 1 Receptor BlockersDiabetes MellitusHumansPublication BiasRenal InsufficiencyAngiotensin-Converting Enzyme InhibitorsAngiotensin II Type 1 Receptor BlockersAngiotensin-converting enzyme inhibitorangiotensin II receptor blockerend-stage renal diseasemeta-analysismortalityrenin-angiotensin system

Identifiers

PMID27377659
PMCPMC5843910
OpenAlexW2469312654

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.