Evidence map›Paper›PMID 25684326›Full record

ArticleJournal of cardiovascular electrophysiology2015

Influence of Zoledronic Acid on Atrial Electrophysiological Parameters and Electrocardiographic Measurements.

James E Tisdale, Matthew R Allen, Brian R Overholser, Heather A Jaynes, Richard J Kovacs

Open access · greenAbstract read
In one paragraph

Article in Journal of cardiovascular electrophysiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 27% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Effect of intravenous zoledronic acid infusion on electrocardiographic parameters in patients with osteoporosis.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2016
    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

5 authors at 4 institutions in 1 country.

James E TisdaleDepartment of Pharmacy Practice, College of Pharmacy, Purdue University, Indianapolis, Indiana, USA.
Matthew R AllenDepartment of Anatomy and Cell Biology, Indianapolis, Indiana, USA.
Brian R OverholserDepartment of Pharmacy Practice, College of Pharmacy, Purdue University, Indianapolis, Indiana, USA.
Heather A JaynesDepartment of Pharmacy Practice, College of Pharmacy, Purdue University, Indianapolis, Indiana, USA.
Richard J KovacsKrannert Institute of Cardiology, Department of Medicine, School of Medicine, Indiana University, Indianapolis, Indiana, USA.
Urology of Indiana · USIndiana University · USIndiana University IndianapolisIndiana University – Purdue University Indianapolis · US

Funding

Probing the Atrial Arrhythmogenic Substrate with Sustained Adrenergic StimulationK08HL095655 · NHLBI · PURDUE UNIVERSITY · PI OVERHOLSER, BRIAN R · 2010 to 2014
$691k
Bisphosphonate-related osteonecrosis of the jaw: Bridging the clinical-preclinicaR21DE019686 · NIDCR · INDIANA UNIVERSITY INDIANAPOLIS · PI ALLEN, MATTHEW R · 2009 to 2010
$422k
NHLBI NIH HHS K08 HL095655NIDCR NIH HHS R21 DE019686
6 · The paper itself

Abstract

introductionOur objective was to determine effects of zoledronic acid (ZA) on atrial electrophysiological parameters and electrocardiographic measurements. METHODS AND

resultsEx vivo perfusion study: Isolated guinea pig hearts were perfused with modified Krebs-Henseleit (K-H) buffer with or without ZA 0.07 mg/kg/L (each n = 6). In ZA-perfused hearts, atrial action potential at 90% repolarization (APD90 ) decreased more from baseline than in controls (-23.2% ± -5.1% vs. -2.1% ± -8.1%, P < 0 .0001), as did APD30 (-28.8% ± -3.8% vs. -2.1% ± -2.1%, P < 0.0001). In vivo dose-response study: Guinea pigs underwent intraperitoneal injections every 2 weeks in 1 of 4 groups (each n = 8): ZA 0.007 mg/kg (low-dose), ZA 0.07 mg/kg (medium-dose), ZA 0.7 mg/kg (high-dose), or placebo. Hearts were excised at 8 weeks and perfused with modified K-H. Atrial effective refractory period (ERP) was lower with medium- and high-dose ZA versus placebo (P = 0.004). Atrial APD30 was lower with high-dose ZA versus placebo, low and medium doses (P < 0.001). Canine ECG study: Mature female beagles received intravenous ZA 0.067 mg/kg or saline (placebo; each n = 6) every 2 weeks for 12 weeks. P wave dispersion was greater in the ZA group (7.7 ± 3.7 vs. 3.4 ± 2.6 ms, P = 0.04). There were no significant differences in P wave index, maximum or minimum P wave duration, or PR interval.

conclusionZA shortens left atrial APD and ERP and increases P wave dispersion.

Indexed as

Action PotentialsAnimalsAtrial FibrillationBone Density Conservation AgentsDiphosphonatesDogsDose-Response Relationship, DrugElectrocardiographyFemaleGuinea PigsImidazolesPerfusionRiskZoledronic AcidBone Density Conservation AgentsDiphosphonatesImidazolesZoledronic Acidaction potentialatrial fibrillationbisphosphonateselectrocardiographyPR intervalproarrhythmiaP wavezoledronic acid

Identifiers

PMID25684326
PMCPMC4464904
OpenAlexW2137626448

What OpenQuestion holds

Textmetadata
LicenceTDM
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.