All-cause and cause-specific mortality in atopic dermatitis patients: a systematic review and meta-analysis.
메타분석
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
환자: atopic dermatitis (AD)
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Future research should incorporate more diverse populations and study designs. [PROSPERO IDENTIFIER] CRD420251038553.
[INTRODUCTION] This meta-analysis evaluates the risk of all-cause and cause-specific mortality in patients with atopic dermatitis (AD).
- HR 1.222
- 연구 설계 meta-analysis
APA
Yang Y, Zhang Q, et al. (2026). All-cause and cause-specific mortality in atopic dermatitis patients: a systematic review and meta-analysis.. Expert review of clinical immunology, 22(1), 135-143. https://doi.org/10.1080/1744666X.2026.2618271
MLA
Yang Y, et al.. "All-cause and cause-specific mortality in atopic dermatitis patients: a systematic review and meta-analysis.." Expert review of clinical immunology, vol. 22, no. 1, 2026, pp. 135-143.
PMID
41560609 ↗
Abstract 한글 요약
[INTRODUCTION] This meta-analysis evaluates the risk of all-cause and cause-specific mortality in patients with atopic dermatitis (AD).
[METHODS] A systematic search of PubMed, EMBASE, and the Cochrane Library (from inception to April 2025) was conducted for cohort studies comparing mortality risks in AD patients versus controls, in accordance with PRISMA guidelines. Two reviewers screened studies, extracted data, and assessed quality using the Newcastle-Ottawa Scale. Hazard ratios (HRs) were calculated using random-effects models in Stata 14.0, with sensitivity analyses, subgroup analyses, and publication bias assessments.
[RESULTS] Nine cohort studies were included. AD patients had significantly increased risks of all-cause mortality [HR = 1.222, 95% CI (1.117-1.336)], as well as mortality due to infectious diseases [HR = 1.606, CI (1.087-2.372)], cancer [HR = 1.129, CI (1.015-1.256)], respiratory diseases [HR = 1.381, CI (1.044-1.825)], and gastrointestinal diseases [HR = 1.658, CI (1.002-2.743)]. Subgroup analyses revealed a higher risk of all-cause mortality in prospective studies compared to retrospective studies, with significantly higher risks in studies from Europe and Asia.
[CONCLUSIONS] AD is associated with an elevated risk of all-cause and cause-specific mortality, underscoring the need for improved monitoring and targeted interventions. Future research should incorporate more diverse populations and study designs.
[PROSPERO IDENTIFIER] CRD420251038553.
[METHODS] A systematic search of PubMed, EMBASE, and the Cochrane Library (from inception to April 2025) was conducted for cohort studies comparing mortality risks in AD patients versus controls, in accordance with PRISMA guidelines. Two reviewers screened studies, extracted data, and assessed quality using the Newcastle-Ottawa Scale. Hazard ratios (HRs) were calculated using random-effects models in Stata 14.0, with sensitivity analyses, subgroup analyses, and publication bias assessments.
[RESULTS] Nine cohort studies were included. AD patients had significantly increased risks of all-cause mortality [HR = 1.222, 95% CI (1.117-1.336)], as well as mortality due to infectious diseases [HR = 1.606, CI (1.087-2.372)], cancer [HR = 1.129, CI (1.015-1.256)], respiratory diseases [HR = 1.381, CI (1.044-1.825)], and gastrointestinal diseases [HR = 1.658, CI (1.002-2.743)]. Subgroup analyses revealed a higher risk of all-cause mortality in prospective studies compared to retrospective studies, with significantly higher risks in studies from Europe and Asia.
[CONCLUSIONS] AD is associated with an elevated risk of all-cause and cause-specific mortality, underscoring the need for improved monitoring and targeted interventions. Future research should incorporate more diverse populations and study designs.
[PROSPERO IDENTIFIER] CRD420251038553.
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