Evidence map›Paper›PMID 29545262›Full record

ArticleJournal of the American Heart Association2018

Downregulation of L-Type Voltage-Gated Ca

Bailin Liu, Ruixiu Shi, Xiang Li, Yanping Liu, Xueqin Feng, Xueyi Chen, Xiaorong Fan, Yingying Zhang, Wenna Zhang, Jiaqi Tang and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 8% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Guideline
  2. Review
  3. Article
  4. Review
  5. Article
  6. 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

14 authors at 2 institutions in 2 countries.

Bailin LiuInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Ruixiu ShiInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Xiang LiInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Yanping LiuInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Xueqin FengInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Xueyi ChenInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Xiaorong FanInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Yingying ZhangInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Wenna ZhangInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Jiaqi TangInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Xiuwen ZhouInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Na LiInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Xiyuan LuInstitute for Fetology, First Hospital of Soochow University, Suzhou, China xuzhice@suda.edu.cn luxiyuan2017@suda.edu.cn.
Zhice XuInstitute for Fetology, First Hospital of Soochow University, Suzhou, China xuzhice@suda.edu.cn luxiyuan2017@suda.edu.cn.
First Affiliated Hospital of Soochow University · CNSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrenatal hypoxia is suggested to be associated with increased risks of hypertension in offspring. This study tested whether prenatal hypoxia resulted in salt-sensitive offspring and its related mechanisms of vascular ion channel remodeling. METHODS AND

resultsPregnant rats were housed in a normoxic (21% O

conclusionsThe results demonstrated that chronic prenatal hypoxia may program salt-sensitive hypertension in male offspring, providing new information of ion channel remodeling in hypertensive myocytes. This information paves the way for early prevention and treatments of salt-induced hypertension related to developmental problems in fetal origins.

Indexed as

Blood PressurePrenatal Exposure Delayed EffectsSodium Chloride, DietaryAnimalsCalcium Channels, L-TypeCalcium SignalingDown-RegulationFemaleGestational AgeHypertensionHypoxiaLarge-Conductance Calcium-Activated Potassium Channel beta SubunitsMaleMembrane PotentialsMesenteric ArteriesMuscle, Smooth, VascularCACNA1C protein, mouseCalcium Channels, L-TypeKcnb1 protein, ratLarge-Conductance Calcium-Activated Potassium Channel beta SubunitsShab Potassium ChannelsSodium Chloride, Dietaryarterialhigh salthypertensionion channelsL‐type calcium channelsmesenteric arteryperinatal hypoxiaprenatal hypoxiavoltage‐gated potassium channels

Identifiers

PMID29545262
PMCPMC5907567
OpenAlexW2790757386

What OpenQuestion 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 OpenQuestion graph.