Evidence map›Paper›PMID 36495935›Full record

ArticleThe American journal of medicine2023

Renin-Angiotensin System-Modifying Antihypertensive Drugs Can Reduce the Risk of Cardiovascular Complications in Lupus: A Retrospective Cohort Study.

Chelsie Hurst, Maira Soto, Ernest R Vina, Kathleen E Rodgers

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 10 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

4 authors at 2 institutions in 1 country.

Chelsie HurstDepartment of Pharmacology, Center for Innovation in Brain Science, College of Medicine, University of Arizona, Tucson.
Maira SotoDepartment of Pharmacology, Center for Innovation in Brain Science, College of Medicine, University of Arizona, Tucson.
Ernest R VinaSection of Rheumatology, Lewis Katz School of Medicine, Temple University, Philadelphia, Pa.
Kathleen E RodgersDepartment of Pharmacology, Center for Innovation in Brain Science, College of Medicine, University of Arizona, Tucson. Electronic address: krodgers@arizona.edu.
University of Arizona · USTemple University · US

Funding

Timing of Menopausal Hormone Therapy across Perimenopause to Menopause Transition: Neuroimmune System in BrainP01AG026572 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ROBERTA EILEEN BRINTON · 2006 to 2026
$53.7M
Undergraduate Readying for Burgeoning Research for American Indian NeuroscientistsR25NS107185 · NINDS · UNIVERSITY OF ARIZONA · PI BRINTON, ROBERTA EILEEN, RODGERS, KATHLEEN E. · 2019 to 2023
$1.5M
NIA NIH HHS P01 AG026572NINDS NIH HHS R25 NS107185
6 · The paper itself

Abstract

backgroundPatients with systemic lupus erythematosus have a higher incidence of cardiovascular disease than the general population. Antihypertensive drugs that modify the renin-angiotensin system (RAS) are used to protect renal function in lupus nephritis and may also have extrarenal effects that lower cardiovascular disease risk due to their anti-inflammatory properties. In this study, we compared the effects of RAS vs non-RAS antihypertensive drugs on cardiovascular disease incidence in patients with lupus.

methodsUsing a medical insurance claims dataset, 220,168 patients with lupus were identified, of which 31,647 patients (4018 patients prescribed RAS drugs, 27,629 patients prescribed non-RAS drugs) were eligible for the study. Patients had a mean age of 46.1 years, were 93.0% female, and healthy (96.9% Charlson Comorbidity Index score 0-4). Patients in the 2 drug groups were propensity score matched using demographic data, risk factors, and comorbidities.

resultsUse of RAS vs non-RAS drugs lowered the relative risk (RR) of diagnosis of cardiovascular disease (RR 0.80; 95% confidence interval [CI], 0.74-0.87), which was more pronounced after propensity score matching (RR 0.62; 95% CI, 0.57-0.68). The decreased risk in cardiovascular disease occurred regardless of lupus nephritis status (with lupus nephritis: RR 0.51; 95% CI, 0.39-0.65; without lupus nephritis: RR 0.65; 95% CI, 0.59-0.72). RAS-modifying therapies significantly increased cardiovascular disease-free survival probability over a 5-year period (86.0% vs 78.3% probability).

conclusionsRAS-modifying drugs reduced the risk of cardiovascular disease in patients with systemic lupus erythematosus in this dataset. These findings have the potential to impact clinical decision-making with regards to hypertension management in patients with lupus.

Indexed as

Cardiovascular DiseasesHypertensionLupus NephritisAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsAntihypertensive AgentsFemaleHumansMaleMiddle AgedRenin-Angiotensin SystemRetrospective StudiesRisk FactorsAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsAntihypertensive AgentsACE inhibitors (ACE-I)Angiotensin receptor blockers (ARB)Cardiovascular diseaseInsurance claims databaseRenin-angiotensin system (RAS)Retrospective cohort studySystemic lupus erythematosus

Identifiers

PMID36495935
PMCPMC9957968
OpenAlexW4311114312

What OpenQuestion holds

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Registered trials

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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.