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Prepubertal to adolescent lupus: Age-related variations in clinical, laboratory, and outcome profiles
Lujayn Akbar1, Majd S Khader2, Rawan Elshaer2
1King Fahd Hospital of the University, Al-Khobar, Saudi Arabia.
Insights
Childhood-onset systemic lupus erythematosus (cSLE) shows age-related variations. Prepubertal onset cSLE has significantly higher mortality, highlighting the need for early diagnosis and intervention in this vulnerable group.
Area of Science:
- Pediatric Rheumatology
- Autoimmune Diseases
- Systemic Lupus Erythematosus
Background:
- Childhood-onset systemic lupus erythematosus (cSLE) is a complex autoimmune condition with varying presentations based on age.
- Existing research on age-related cSLE variations is limited by retrospective designs and single-nation cohorts, leading to inconsistent findings.
- Understanding age-specific differences is crucial for optimizing diagnosis and management of cSLE.
Purpose of the Study:
- To systematically investigate age-related variations in childhood-onset systemic lupus erythematosus (cSLE) across distinct subgroups: prepubertal, peripubertal, and adolescent-onset.
- To compare clinical manifestations, disease activity, damage, and outcomes among these cSLE age groups.
Main Methods:
- A systematic review was conducted following PRISMA guidelines, searching PubMed, Cochrane Library, and Web of Science for studies published between January 2000 and February 2025.
- Eligible studies included those examining age-related variations in cSLE diagnosed before 18 years, with data categorized into prepubertal, peripubertal, and adolescent-onset groups.
- Study quality was assessed using NHLBI criteria, with data extraction and analysis performed by multiple reviewers.
Main Results:
- Of 16,313 screened studies, 13 met inclusion criteria, encompassing 3920 cSLE cases: 11.8% prepubertal, 49.6% peripubertal, and 38.6% adolescent-onset.
- The female-to-male ratio was highest in the adolescent-onset group (p = .002). Musculoskeletal involvement increased with age, while neuropsychiatric symptoms and fever decreased.
- Mortality was significantly higher in the prepubertal group (16.5%) compared to the adolescent-onset group (2.9%) (p = .014), despite similar disease activity and damage across groups.
Conclusions:
- This systematic review highlights significant age-related differences in childhood-onset systemic lupus erythematosus (cSLE), particularly concerning mortality.
- Prepubertal onset cSLE is associated with a substantially higher mortality rate, underscoring the critical need for prompt diagnosis and aggressive early intervention.
- Further research into age-specific management strategies for cSLE is warranted to improve long-term outcomes across all age groups.
Abstract:
BackgroundChildhood-onset systemic lupus erythematosus (cSLE) is a heterogeneous autoimmune disease with age-related variations. Older children often exhibit higher disease activity, whereas early-onset cSLE is associated with worse outcomes. However, most existing studies are retrospective and based on single-nation cohorts, yiedling inconsistent findings.ObjectiveTo investigate age-related variations in cSLE subgroups, namely prepubertal, peripubertal, and adolescent-onset cases.MethodsThis systematic review, registered in PROSPERO and conducted in accordance with PRISMA guidelines, searched PubMed, the Cochrane Library, and Web of Science for English-language studies pubslished between January 2000- February 2025. Eligible studies examined age-related variations in cSLE diagnosed before 18 years of age. Data were categorized into prepubertal, peri-pubertal, and adolescent-onset groups. Exclusion criteria included case reports, comments, editorials, viewpoint articles, conference abstracts, and incomplete studies. Four reviewers independently screened the articles, with discrepancies resolved by a fifth reviewer. Study quality was assessed using the NHLBI criteria.ResultsOf 16,313 studies screened, 13 met the inclusion criteria, comprising a total of 3920 cSLE cases. Among these, 464 (11.8%) were prepubertal, 1943 (49.6%) peripubertal, and 1513 (38.6%) adolescent-onset. The mean age at diagnosis was 5.8 ± 2.3, 9.4 ± 2.5, and 13.9 ± 1.1 years, respectively. The female-to-male ratio was highest in the adolescent-onset group (p = .002). Clinical manifestations showed no significant age-related differences; however, musculoskeletal involvement increased with age, while neuropsychiatric symptoms and fever decreased. Lymphopenia was more frequent in the adolescent-onset group (60% vs 25.6%, p = .016). Although disease activity and damage did not differ significantly across age groups, mortality was signficantly higher in the prepubertal group (16.5%) compared to the adolescent-onset group (2.9%) (p = .014).ConclusionThis review underscores both similarities and differences in cSLE across age groups. Prepubertal onset was associated with higher mortality, emphasizing the need for timely diagnosis and early intervention in this subgroup.
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