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Targeting Rac1 for the prevention of atherosclerosis among U.S. Veterans with inflammatory bowel disease.

Small GTPases 2022 Vol.13(1) p. 205-210

Sutton SS, Magagnoli J, Cummings TH, Hardin JW

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Evidence suggests that Ras-related C3 botulinum toxin substrate 1 (Rac1) might be a target in atherosclerotic disease (AD).

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  • HR 0.925

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BibTeX ↓ RIS ↓
APA Sutton SS, Magagnoli J, et al. (2022). Targeting Rac1 for the prevention of atherosclerosis among U.S. Veterans with inflammatory bowel disease.. Small GTPases, 13(1), 205-210. https://doi.org/10.1080/21541248.2021.1954863
MLA Sutton SS, et al.. "Targeting Rac1 for the prevention of atherosclerosis among U.S. Veterans with inflammatory bowel disease.." Small GTPases, vol. 13, no. 1, 2022, pp. 205-210.
PMID 34320903

Abstract

Evidence suggests that Ras-related C3 botulinum toxin substrate 1 (Rac1) might be a target in atherosclerotic disease (AD). We hypothesize that due to their ability to inhibit Rac1, thiopurines are associated with a lower risk of AD. We fit a time-dependent cox proportional hazards model estimating the hazard of AD among a national cohort of US veterans with inflammatory bowel disease. Patients exposed to thiopurines had a 7.5% lower risk of AD (HR = 0.925; 95% CI = (0.87-0.984)) compared to controls. The propensity score weighted analysis reveals thiopurine exposure reduces the risk of AD by 6.6% (HR = 0.934; 95% CI = (0.896-0.975)), compared to controls. Further exploration and evaluation of Rac1 inhibition as a target for AD is warranted.

추출된 의학 개체 (NER)

유형영어 표현한국어 / 풀이UMLS CUI출처등장
시술 botulinum toxin 보툴리눔독소 주사 dict 1

MeSH Terms

Humans; Immunosuppressive Agents; Veterans; Inflammatory Bowel Diseases; Cohort Studies; Atherosclerosis; rac1 GTP-Binding Protein

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