{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["103(43)"],"submitter":["Wu Y"],"pubmed_abstract":["Cysteine cathepsins are proteolytic enzymes crucial in various physiological and pathological processes, primarily operating within lysosomes. Their functions include protein degradation, immune system regulation, and involvement in various diseases. While some cysteine cathepsins play important roles in the immune system, their connection to autoimmune diseases remains unclear. This study proposes using Mendelian randomization to explore the causal relationship between cysteine cathepsins and autoimmune diseases. Single nucleotide polymorphisms (SNPs) for cysteine cathepsins were obtained from a publicly available genome-wide association study (GWAS) dataset, while outcome SNP data were sourced from 10 separate GWAS datasets. Mendelian randomization (MR) analysis employed the Wald ratio ("],"journal":["Medicine"],"pagination":["e40268"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11521024"],"repository":["biostudies-literature"],"pubmed_title":["Cysteine cathepsins and autoimmune diseases: A bidirectional Mendelian randomization."],"pmcid":["PMC11521024"],"pubmed_authors":["Huang J","Lou Y","Li Q","Wu Y","Zhou Z"],"additional_accession":[]},"is_claimable":false,"name":"Cysteine cathepsins and autoimmune diseases: A bidirectional Mendelian randomization.","description":"Cysteine cathepsins are proteolytic enzymes crucial in various physiological and pathological processes, primarily operating within lysosomes. Their functions include protein degradation, immune system regulation, and involvement in various diseases. While some cysteine cathepsins play important roles in the immune system, their connection to autoimmune diseases remains unclear. This study proposes using Mendelian randomization to explore the causal relationship between cysteine cathepsins and autoimmune diseases. Single nucleotide polymorphisms (SNPs) for cysteine cathepsins were obtained from a publicly available genome-wide association study (GWAS) dataset, while outcome SNP data were sourced from 10 separate GWAS datasets. Mendelian randomization (MR) analysis employed the Wald ratio (","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Oct","modification":"2026-06-03T07:18:57.21Z","creation":"2025-04-06T09:35:56.351Z"},"accession":"S-EPMC11521024","cross_references":{"pubmed":["39470488"],"doi":["10.1097/MD.0000000000040268"]}}