4.7 Article

Milk Fat Globule Epidermal Growth Factor 8 (MFGE8) Gene Variants in Rheumatoid Arthritis and Sjogren's Syndrome

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JOURNAL OF CLINICAL MEDICINE
卷 11, 期 5, 页码 -

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MDPI
DOI: 10.3390/jcm11051180

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MFGE8; systemic lupus erythematosus; rheumatoid arthritis; Sjogren's Syndrome; polymorphisms

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This study found that MFGE8 variants were possibly associated with susceptibility to SS and RA, and that SS patients had reduced MFGE8 serum levels, which were related to increased risk of atherosclerosis.
Milk Fat Globule Epidermal Growth Factor 8 (MFGE8) deficiency and gene polymorphisms have been previously linked to systemic lupus erythematosus (SLE)-like and SLE development. Our aim was to explore whether four MFGE8 variants and MFGE8 serum levels are associated with autoimmunity susceptibility and autoimmune related atherosclerosis. DNA from 107 primary Sjogren's syndrome (SS), 116 rheumatoid arthritis (RA) and 123 SLE patients as well as 199 HC were genotyped for the MFGE8 rs2271715, rs1878326, rs4945, rs3743388 variants by RFLP-PCR. MFGE8 serum levels were measured by ELISA. The CA genotype of rs4945 variant exhibited a protective effect against RA development, a finding not confirmed in the SS and SLE populations. The CACG haplotype exhibited a protective effect in both RA and SS patients compared to HC. Primary SS patients with IMT <= 0.9 mm displayed higher MGFE8 serum levels compared to those with >0.9 mm. Here, we report a novel association of MFGE8 variants in SS and RA susceptibility, as well as reduced MFGE8 serum levels in SS patients with heightened atherosclerotic risk.

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