Evidence map›Paper›PMID 29157100›Full record

ArticleRenal failure2017

Imbalanced plasma ACE and ACE2 level in the uremic patients with cardiovascular diseases and its change during a single hemodialysis session.

Chung-Wei Yang, Li-Che Lu, Chia-Chu Chang, Ching-Chang Cho, Wen-Yeh Hsieh, Chin-Hung Tsai, Yi-Chang Lin, Chih-Sheng Lin

Open access · goldAbstract read
In one paragraph

Article in Renal failure, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 2 pooled it
1.1field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 2 syntheses or guidelines pooled it, 27 citations in OpenAlex.

  1. Pooled it
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  7. Medicina (Kaunas, Lithuania) · 2023
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  11. COVID-19: angiotensin-converting enzyme 2 (ACE2) expression and tissue susceptibility to SARS-CoV-2 infection.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2021
    Review
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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 3 institutions in 1 country.

Chung-Wei Yanga Department of Biological Science and Technology , National Chiao Tung University , Hsinchu , Taiwan.ORCID http://orcid.org/0000-0002-8613-3597
Li-Che Luc Division of Nephrology, Department of Internal Medicine , Shin Kong Wu Ho-Su Memorial Hospital , Taipei , Taiwan.
Chia-Chu Changd Division of Nephrology, Department of Internal Medicine , Changhua Christian Hospital , Changhua , Taiwan.
Ching-Chang Choa Department of Biological Science and Technology , National Chiao Tung University , Hsinchu , Taiwan.ORCID http://orcid.org/0000-0002-5087-3542
Wen-Yeh Hsiehf Division of Chest Medicine, Department of Internal Medicine , Hsinchu Mackay Memorial Hospital , Hsinchu , Taiwan.
Chin-Hung Tsaia Department of Biological Science and Technology , National Chiao Tung University , Hsinchu , Taiwan.
Yi-Chang Lina Department of Biological Science and Technology , National Chiao Tung University , Hsinchu , Taiwan.
Chih-Sheng Lina Department of Biological Science and Technology , National Chiao Tung University , Hsinchu , Taiwan.ORCID http://orcid.org/0000-0002-1609-7594
National Yang Ming Chiao Tung University · TWChanghua Christian Hospital · TWMinghsin University of Science and Technology · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe renin-angiotensin system (RAS) has significant influences on heart and renal disease progression. Angiotensin converting enzyme (ACE) and angiotensin converting enzyme II (ACE2) are major peptidases of RAS components and play counteracting functions through angiotensin II (Ang II)/ATIR and angiotensin-(1-7) (Ang-(1-7))/Mas axis, respectively.

methodsThere were 360 uremic patients on regular hemodialysis (HD) treatment (inclusive of 119 HD patients with cardiovascular diseases (CVD) and 241 HD patients without CVD and 50 healthy subjects were enrolled in this study. Plasma ACE, ACE2, Ang II and Ang-(1-7) levels of the HD patients were determined.

resultsWe compared pre-HD levels of plasma ACE, ACE2, Ang II and Ang-(1-7) in the HD patients with and without CVD to those of the controls. The HD patients, particularly those with CVD, showed a significant increase in the levels of ACE and Ang II, whereas ACE2 and Ang-(1-7) levels were lower than those in the healthy controls. Therefore, imbalanced ACE/ACE2 was observed in the HD patients with CVD. In the course of a single HD session, the plasma ACE, ACE/ACE2 and Ang II levels in the HD patients with CVD were increased from pre-HD to post-HD. On the contrary, ACE2 levels were decreased after the HD session. These changes were not detected in the HD patients without CVD.

conclusionsPathogenically imbalanced circulating ACE/ACE2 was detected in the HD patients, particularly those with CVD. HD session could increase ACE/Ang II/AT1R axis and decrease ACE2/Ang-(1-7)/Mas axis activity in the circulation of HD patients with CVD.

Indexed as

AgedAged, 80 and overAngiotensin-Converting Enzyme 2Cardiovascular DiseasesFemaleHumansKidney Failure, ChronicMaleMiddle AgedPeptidyl-Dipeptidase AProspective StudiesUremiaACE2 protein, humanAngiotensin-Converting Enzyme 2Peptidyl-Dipeptidase AAngiotensin converting enzymeangiotensin converting enzyme IIcardiovascular diseaseshemodialysisrenin-angiotensin systemuremic patient

Identifiers

PMID29157100
PMCPMC6446170
OpenAlexW2769223956

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.