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Mendelian Randomization Analysis Reveals a Complex Genetic Interplay among Atopic Dermatitis, Asthma, and Gastroesophageal Reflux Disease

Kwangmi Ahn, Raymond B. Penn, Satish Rattan, Reynold A. Panettieri, Benjamin F. Voight, Steven S. An

2022American Journal of Respiratory and Critical Care Medicine58 citationsDOIOpen Access PDF

Abstract

Abstract Rationale Gastroesophageal reflux disease (GERD) is commonly associated with atopic disorders, but cause–effect relationships remain unclear. Objectives We applied Mendelian randomization analysis to explore whether GERD is causally related to atopic disorders of the lung (asthma) and/or skin (atopic dermatitis [AD]). Methods We conducted two-sample bidirectional Mendelian randomization to infer the magnitude and direction of causality between asthma and GERD, using summary statistics from the largest genome-wide association studies conducted on asthma (N cases = 56,167) and GERD (N cases = 71,522). In addition, we generated instrumental variables for AD from the latest population-level genome-wide association study meta-analysis (N cases = 22,474) and assessed their fidelity and confidence of predicting the likely causal pathway(s) leading to asthma and/or GERD. Measurements and Main Results Applying three different methods, each method revealed similar magnitude of causal estimates that were directionally consistent across the sensitivity analyses. Using an inverse variance–weighted method, the largest effect size was detected for asthma predisposition to AD (odds ratio [OR], 1.46; 95% confidence interval [CI], 1.34–1.59), followed by AD to asthma (OR, 1.34; 95% CI, 1.24–1.45). A significant association was detected for genetically determined asthma on risk of GERD (OR, 1.06; 95% CI, 1.03–1.09) but not genetically determined AD on GERD. In contrast, GERD equally increased risks of asthma (OR, 1.21; 95% CI, 1.09–1.35) and AD (OR, 1.21; 95% CI, 1.07–1.37). Conclusions This study uncovers previously unrecognized causal pathways that have clinical implications in European-ancestry populations: 1) asthma is a causal risk for AD, and 2) the predisposition to AD, including asthma, can arise from specific pathogenic mechanisms manifested by GERD.

Topics & Concepts

Mendelian randomizationGERDMedicineAsthmaOdds ratioAtopic dermatitisGenome-wide association studyPopulationConfidence intervalDiseaseInternal medicineImmunologySingle-nucleotide polymorphismRefluxGeneticsEnvironmental healthGenotypeBiologyGenetic variantsGeneEosinophilic EsophagitisAsthma and respiratory diseasesIL-33, ST2, and ILC Pathways