Mortality and survival in patients with systemic lupus erythematosus in the Middle East and North Africa: a systematic review and meta-analysis
Clinical Snapshot
PICO Framework
| P — Population | Adult patients with systemic lupus erythematosus (SLE) residing in the Middle East and North Africa (MENA) region |
| I — Intervention | Cohort follow-up of SLE patients, including treatment exposures (corticosteroids, cyclophosphamide, hydroxychloroquine, azathioprine) |
| C — Comparator | Comparisons across studies, time points (5, 10, 15, 20 years), and treatment exposures; no explicit general-population comparator arm in all studies |
| O — Outcomes | All-cause mortality rate, survival rates at 5, 10, 15, and 20 years, predictors of mortality (renal, cardiovascular, infectious, haematologic, demographic), and cause-specific mortality |
Bottom Line
This systematic review and meta-analysis provides the first pooled regional estimate of SLE mortality in the MENA region, drawing on 12 cohort studies and 3,478 patients from five countries. The pooled all-cause mortality rate of 9.9% (95% CI: 7.2%–14.0%) and high short-term survival (93.9% at 5 years) are broadly consistent with global SLE literature, but the very high heterogeneity (I² = 89.7%) and instability of long-term estimates on sensitivity analysis substantially limit confidence in these figures. Infection emerged as the leading cause of death, followed by active disease, renal failure, and cardiovascular complications — findings that are clinically actionable regardless of the statistical limitations. The protective associations of hydroxychloroquine and azathioprine, and the harm signal from high cumulative corticosteroid and cyclophosphamide exposure, reinforce existing treatment optimisation principles. For Australian clinicians managing patients of MENA background, these findings support vigilance for renal and cardiovascular complications, aggressive infection prevention strategies, and maximising hydroxychloroquine use. The review's geographic gaps — notably the absence of Saudi Arabia and most Arab states — and the lack of GRADE assessment mean this evidence should inform clinical awareness rather than drive guideline revision. Multicenter MENA registries are urgently needed.
Key Findings
P Value: Not reported in abstract
Effect Size: Pooled all-cause mortality rate: 9.9%; Survival: 93.9% at 5 years, 90.0% at 10 years, 85.5% at 15 years, 71.7% at 20 years
Primary Outcome: Pooled all-cause mortality rate in adult SLE patients across MENA region (12 cohort studies, n=3,478)
Nnt Or Sensitivity: Prognostic study: no NNT applicable. Key mortality predictors include renal involvement, cardiovascular disease, infections, hypertension, diabetes, haematologic abnormalities, and male sex. Hydroxychloroquine and azathioprine associated with reduced mortality; higher cumulative corticosteroids and cyclophosphamide associated with increased mortality. I² = 89.7% for primary pooled estimate.
Confidence Interval: All-cause mortality 95% CI: 7.2%–14.0%; CIs for individual survival time points not reported in abstract
Clinical Application
The identified mortality predictors (renal involvement, cardiovascular risk, infection burden, male sex) are clinically actionable using existing monitoring frameworks. Optimisation of hydroxychloroquine use and minimisation of cumulative corticosteroid exposure are feasible within current rheumatology practice. Establishment of multicenter MENA registries, as recommended by the authors, would require significant infrastructure investment. Australia has a growing MENA-origin population, and SLE prevalence and severity may differ from the predominantly European cohorts underpinning current RACGP and Australian Rheumatology Association guidelines. Hydroxychloroquine is PBS-listed for SLE (PBS item 5261K) and its protective association reinforces current prescribing practice. Azathioprine is also PBS-listed as a steroid-sparing agent. The finding that infection is the leading cause of death aligns with Australian immunosuppression stewardship priorities. Clinicians managing MENA-background SLE patients should be alert to potentially higher renal involvement rates and ensure nephrology co-management pathways are in place. The TGA-approved biologics (belimumab) for SLE are not addressed in this review. RACGP chronic disease management plans should incorporate cardiovascular risk reduction given the identified cardiovascular mortality burden. Adult patients with SLE, particularly those of Middle Eastern, North African, or broadly non-European ethnic backgrounds. Findings are most directly applicable to patients from Türkiye, Iran, Egypt, Israel, and Tunisia. Caution is warranted in extrapolating to other MENA populations not represented in the included studies.
Abstract
Systemic lupus erythematosus (SLE) is associated with increased mortality compared with the general population, with outcomes influenced by ethnicity and organ involvement. Data from the Middle East and North Africa (MENA) remain limited, particularly regarding long-term survival and mortality predictors. To estimate and compare all-cause mortality and survival rates among adult patients with SLE in the MENA region and identify predictors of mortality. A systematic review and meta-analysis of cohort studies reporting survival and mortality in patients with SLE in the MENA region was conducted. Eligible studies were identified through a comprehensive database search and screened according to PRISMA guidelines. Data on treatment exposures and clinical predictors of mortality were extracted. Twelve cohort studies, including 3,478 adults with SLE from five MENA countries (Türkiye, Iran, Egypt, Israel, and Tunisia), were analyzed. The pooled all-cause mortality rate was 9.9% (95% CI: 7.2%-14.0%; I² = 89.7%). Survival remained high at 5 years (93.9%) and 10 years (90.0%), but declined at 15 years (85.5%) and 20 years (71.7%), with long-term estimates highly sensitive to single-study exclusion. Leave-one-out analysis slightly increased survival estimates and reduced heterogeneity. Major mortality predictors included renal involvement, cardiovascular disease, infections, hypertension, diabetes, hematologic abnormalities, and male sex. Higher cumulative corticosteroid and cyclophosphamide exposure was linked to increased mortality, whereas hydroxychloroquine and azathioprine appeared protective. Infection was the leading cause of death, followed by active disease, renal failure, and cardiovascular complications. Patients with SLE in the MENA region show high short-term survival, but long-term outcomes remain variable. Mortality is mainly driven by renal, cardiovascular, and infectious complications, with treatment exposure contributing to risk. These findings highlight the need for multicenter registries, standardized reporting, and strategies to reduce infection burden and optimize nephritis care.
References
- 1.Alharbi, S., & Aljohani, R. (2026). Mortality and survival in patients with systemic lupus erythematosus in the Middle East and North Africa: a systematic review and meta-analysis. Rheumatology International. https://doi.org/10.1007/s00296-019-04484-9
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