Evidence map›Paper›PMID 36315490›Full record

ArticleAmerican journal of hypertension2023

Baseline Serum Biomarkers of Inflammation and Subsequent Visit-to-Visit Blood Pressure Variability: A Post Hoc Analysis of MESA.

Ka-Ho Wong, Varsha Muddasani, Cecilia Peterson, Nazanin Sheibani, Cameron Arkin, Irene Cheong, Jennifer J Majersik, Alessandro Biffi, Nils Petersen, Guido J Falcone and 2 more

Open access · greenAbstract read
In one paragraph

Article in American journal of hypertension, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-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

6 citing papers in PubMed, 8 citations in OpenAlex.

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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

12 authors at 5 institutions in 1 country.

Ka-Ho WongDepartment of Neurology, University of Utah, Salt Lake City, Utah, USA.ORCID 0000-0001-9597-8105
Varsha MuddasaniDepartment of Neurology, Einstein Healthcare Network, Philadelphia, Pennsylvania, USA.
Cecilia PetersonDepartment of Neurology, University of Utah, Salt Lake City, Utah, USA.
Nazanin SheibaniDepartment of Neurology, Tufts Medical Center, Boston, Massachusetts, USA.
Cameron ArkinDepartment of Neurology, University of Utah, Salt Lake City, Utah, USA.
Irene CheongDepartment of Internal Medicine, University of Utah, Salt Lake City, Utah, USA.
Jennifer J MajersikDepartment of Neurology, University of Utah, Salt Lake City, Utah, USA.
Alessandro BiffiDepartment of Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Nils PetersenDepartment of Neurology, Yale University, New Haven, Connecticut, USA.
Guido J FalconeDepartment of Neurology, Yale University, New Haven, Connecticut, USA.
Lauren H SansingDepartment of Neurology, Yale University, New Haven, Connecticut, USA.
Adam H de HavenonDepartment of Neurology, Yale University, New Haven, Connecticut, USA.
University of Utah · USYale University · USEinstein Healthcare Network · USMassachusetts General Hospital · USTufts Medical Center · US

Funding

Precision blood pressure management after endovascular stroke therapy based on real-time autoregulation measurementsK23NS110980 · NINDS · YALE UNIVERSITY · PI PETERSEN, NILS H. · 2020 to 2024
$951k
NINDS NIH HHS K23 NS110980
6 · The paper itself

Abstract

backgroundHigher blood pressure variability (BPV) is associated with the development of major vascular diseases, independent of mean blood pressure. However, despite data indicating that serum inflammatory markers are linked to hypertension, the association between serum inflammatory markers and BPV has not been studied in humans.

methodsThis is a post hoc analysis of the Multi-Ethnic Study of Atherosclerosis (MESA) study. The study exposure was tertiles of serum level of interleukin-6 (IL-6), C-reactive protein (CRP), d-dimer, plasmin-antiplasmin complex (PAP), fibrinogen antigen, and calibrated Factor VIII (%) at the baseline study visit. The primary outcome was visit-to-visit BPV measured as the residual standard deviation (rSD) of at least 4 study visits (2000-2018). Two logistic regression models were fit to the top tertile of rSD during follow-up: in Model 1, we adjusted for age, sex, and hypertension, and in Model 2, for patient age categories, sex, race/ethnicity, education, hypertension, diabetes, smoking, drinking, body mass index, lipid-lowering medication, and mean systolic blood pressure.

resultsOur analysis included 5,483 patients, with a mean (SD) age of 61.4 (10.0) years, 52.9% female, and 40.7% White. In unadjusted analyses, all markers of inflammation were associated with higher BPV, but after adjustment, only IL-6 retained significance (P < 0.001). The odds ratio for the highest tertile of BPV and IL-6 was 1.49 (95% confidence interval [CI] 1.28-1.74, P < 0.001).

conclusionsBaseline serum IL-6 was associated with increased subsequent BPV in a large multiracial cohort. Further investigation is needed to better understand the relationship between chronic inflammation and BPV.

Indexed as

AtherosclerosisHypertensionBiomarkersBlood PressureFemaleHumansInflammationInterleukin-6MaleMiddle AgedBiomarkersInterleukin-66angiotensinantiplasmin complexblood pressureblood pressure variabilityCEthnic Study of AtherosclerosishypertensionIIinterleukinMultiplasminreactive proteinresidual standard deviation

Identifiers

PMID36315490
PMCPMC11484580
OpenAlexW4307779017

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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.