Evidence mapPaperPMID 42568564Full record

Observational studyFrontiers in immunology2026

Systemic lupus erythematosus-related mortality declined but disparities persisted in the United States: a nationwide multiple-cause-of-death analysis, 1999-2023.

Yuhuan Song, Yan Zhang, Li Luo, Xiuju Yang, Kaide Xia

Abstract readObservational Study
In one paragraph

Observational study in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yuhuan Song *Department of Nephrology, Aerospace Center Hospital, Beijing, China.
Yan Zhang *Department of Nephrology, Aerospace Center Hospital, Beijing, China.
Li Luo *School of Public Health, Guizhou Medical University, Guiyang, China.
Xiuju YangDepartment of Clinical Laboratory, The Second People's Hospital of Guiyang, Guiyang, China.
Kaide XiaDepartment of Clinical Laboratory, The Second People's Hospital of Guiyang, Guiyang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Systemic lupus erythematosus (SLE) causes substantial premature mortality. Contemporary national data on long-term SLE-related mortality and its demographic and geographic disparities in the United States remain limited, particularly across the transition into the COVID-19 era. Methods: We conducted a nationwide observational study using the 1999-2023 CDC WONDER Multiple Cause of Death database. SLE-related mortality was defined as any death certificate mention of SLE (ICD-10 M32). An underlying-cause-only sensitivity analysis assessed trend robustness. Annual deaths and age-adjusted mortality rates (AAMRs) were examined overall and by sex, age, race, geography, and urbanization. Temporal trends were evaluated using joinpoint regression to estimate annual percent changes (APCs) and average annual percent changes (AAPCs). Pooled state-level AAMRs were compared between 2016-2019 and 2020-2023. Results: From 1999 to 2023, the national SLE-related AAMR declined from 1.03 to 0.73 per 100,000 (overall AAPC, -1.46%), while annual deaths increased slightly from 2,197 to 2,291. Joinpoint analysis identified a significant decline during 1999-2014, an increase during 2014-2021, and a sharp decline during 2021-2023. Women consistently had higher AAMRs than men. Adults aged ≥65 years had the highest mortality burden with little overall improvement. Black individuals maintained the highest AAMRs throughout, despite experiencing the steepest long-term decline. Geographically, the South, HHS Region 6, and Oklahoma remained high-burden areas. Nonmetropolitan areas showed smaller overall declines and steeper late-period increases. The underlying-cause-only sensitivity analysis also showed an AAMR decline from 0.59 to 0.29 per 100,000 (AAPC, -3.23%). Conclusion: U.S. SLE-related mortality declined overall from 1999 to 2023, but the absolute burden remained substantial and unequally distributed across demographic and geographic strata. Persistent excess mortality among women, older adults, Black individuals, and residents of high-burden areas highlights the need for more equitable translation of advances in lupus care into real-world survival gains.

Indexed as

Health Status DisparitiesLupus Erythematosus, SystemicAdultAgedCause of DeathFemaleHumansMaleMiddle AgedUnited StatesCDC WONDERhealth disparitiesimmune dysregulationmortalitymultiple cause of deathsystemic lupus erythematosus

Identifiers

PMID42568564
PMCPMC13447312

What Socratic holds

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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 Socratic graph.