Evidence map›Paper›PMID 38789277›Full record

ArticleLupus science & medicine2024

Prevalence of major adverse cardiovascular events among Saudi patients with systemic lupus erythematosus compared with the general population: updates from the national SLE and PURE cohorts.

Ibrahim Almaghlouth, Kawther Ghassan Bohuliga, Boshra Alanazi, Bushra Khaled Alhawsa, Abdulaziz Mohammed Alabdulkareem, Wael Alqarawi, Kazi Nur Asfina, Najma Khalil, Hebatallah Hamed Ali, Mohammed Bedaiwi and 9 more

Abstract read
In one paragraph

Article in Lupus science & medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. 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

19 authors.

Ibrahim Almaghlouth *Rheumatology Unit, Department of Medicine, King Saud University, Riyadh, Saudi Arabia.
Kawther Ghassan Bohuliga *Rheumatology Unit, Department of Medicine, King Saud University, Riyadh, Saudi Arabia.
Boshra AlanaziRheumatology Unit, Department of Medicine, King Saud University, Riyadh, Saudi Arabia.
Bushra Khaled AlhawsaRheumatology Unit, Department of Medicine, King Saud University, Riyadh, Saudi Arabia.
Abdulaziz Mohammed AlabdulkareemRheumatology Unit, Department of Medicine, King Saud University, Riyadh, Saudi Arabia.
Wael AlqarawiDepartment of Cardiac Sciences, King Fahad Cardiac Center, College of Medicine, King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia.
Kazi Nur AsfinaCollege of Medicine Research Centre, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Najma KhalilCollege of Medicine Research Centre, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Hebatallah Hamed AliCollege of Medicine Research Centre, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Mohammed BedaiwiRheumatology Unit, Department of Medicine, King Saud University, Riyadh, Saudi Arabia.
Aos AboabatRheumatology Unit, Department of Medicine, King Saud University, Riyadh, Saudi Arabia.ORCID 0000-0003-2468-4171
Jiandong SuUniversity Health Network, University of Toronto, Toronto, Ontario, Canada.
Tariq Asef AlamEmergency Medicine, Norfolk and Norwich University Hospital, Norwich, UK.
Fehaid Ghali AlanaziRheumatology Unit, Department of Medicine, King Saud University, Riyadh, Saudi Arabia.
Mohammed A OmairRheumatology Unit, Department of Medicine, King Saud University, Riyadh, Saudi Arabia.
Abdurhman S AlarfajRheumatology Unit, Department of Medicine, King Saud University, Riyadh, Saudi Arabia.
Haya M AlmalagDepartment of Clinical Pharmacy, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia halmalaq@ksu.edu.sa.ORCID 0000-0001-8531-556X
Mostafa Al ShamiriDepartment of Cardiac Sciences, King Fahad Cardiac Center, College of Medicine, King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia.
Khalid F AlhabibDepartment of Cardiac Sciences, King Fahad Cardiac Center, College of Medicine, King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study examined the prevalence of major adverse cardiovascular events (MACE) among Saudi patients with SLE and the general population and considered factors associated with such outcomes were taken into consideration.

methodsThis is a cohort study evaluating the period prevalence of MACE from 2020 to 2023. The study used two datasets, namely the Saudi national prospective cohort for SLE patients and the Prospective Urban-Rural Epidemiology Study Saudi subcohort (PURE-Saudi) for the general population. Participants in both studies were monitored using a standardised protocol. MACE was defined as myocardial infarction (MI), stroke or angina. The analysis was adjusted for demographics, traditional cardiovascular risk factors and SLE diagnosis through logistic regression models.

resultsThe PURE and national SLE cohorts comprised 488 and 746 patients, respectively. Patients with SLE from the SLE cohort were younger (40.7±12.5 vs 49.5±8.6 years) and predominantly female (90.6% vs 41.6%). The prevalence of traditional risk factors was greater in the PURE cohort compared with the SLE cohort. These factors included dyslipidaemia (28.9% vs 49.4%), obesity (63% vs 85%) and diabetes (7.8% vs 27.2%), but not hypertension (19.3% vs 18.8%). MACE (defined as MI or stroke or venous thromboembolism or heart failure) occurred more frequently in patients with SLE (4.3% vs 1.6%, p=0.004). Older age and lupus diagnosis were independently associated with MACE after adjusting for conventional risk factors. The odds of MACE were significantly related to age and lupus diagnosis (p=0.00 and p=0.00, respectively), but not cardiovascular disease (CVD) risk factors (p=0.83).

conclusionPatients with SLE have a significantly higher risk of developing MACE than the general population. This risk is not well explained by traditional risk factors, which may explain the failure of CVD risk scores to stratify patients with SLE adequately. Further studies are needed to understand CVD risk's pathogenesis in SLE and mitigate it.

Indexed as

Cardiovascular DiseasesLupus Erythematosus, SystemicAdultCohort StudiesDyslipidemiasFemaleHumansMaleMiddle AgedMyocardial InfarctionObesityPrevalenceProspective StudiesRisk FactorsSaudi ArabiaStrokeCardiovascular DiseasesLupus Erythematosus, SystemicPrevalence

Identifiers

PMID38789277
PMCPMC11129032

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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.