ID
45233
Descrizione
Principal Investigator: Nancy Brown, MD, Vanderbilt University Medical Center, Nashville, TN, USA MeSH: Angioedema https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000438 The purpose of this study is to identify genetic predictors of ACE inhibitor-associated angioedema. In addition to preventing the formation of the pressor angiotensin II, ACE inhibitors prevent the carboxyl-terminal degradation of the vasoactive substances bradykinin and substance P. Angioedema is hypothesized to result from defective amino-terminal degradation of bradykinin or substance P in patients in whom ACE is inhibited. For example, activity of dipeptidyl peptidase IV (DPP-IV), the enzyme responsible for the inactivation of substance P when ACE is inhibited, is decreased in patients with angioedema. In preliminary studies, we have identified SNPs in the DPP4 gene that associate with DPP-IV activity and, in blacks, with risk of angioedema. This project will use genome-wide genotyping to compare 250 cases and 568 ACE inhibitor-exposed control subjects (131 cases and 288 controls ascertained at Vanderbilt and 70 cases and 280 controls ascertained at the Marshfield Clinic). We plan a 2-stage analysis of associations between SNPs and angioedema - first, we will study DPP4 SNPs for association with angioedema and, second, we will explore associations using the full GWAS data set. Depending on the platform, additional DPP4 SNPs will be used to fully tag common genetic variants in both African American and European American samples. Based on the HapMap data, there are 14 tagging SNPs in people of European descent and 34 in Yoruba (selection criteria MAF0.05 and r20.8). Cases were defined as having ACE inhibitor-associated angioedema if they had had swelling of the lips, throat, tongue or face while taking an ACE inhibitor but had never had angioedema while not taking an ACE inhibitor. For simplicity, intestinal edema was excluded. Control subjects were treated for at least 6 months with an ACE inhibitor without angioedema. Because black Americans are known to be overrepresented among patients with ACE inhibitor-associated angioedema, control subjects were prespecified to be 50% black American, 50% white American, and 50% female. At Vanderbilt, the medical history, including the history of angioedema, was confirmed by a research nurse or physician using a detailed case report form. Characteristics of Vanderbilt cases appear in the Table. At Marshfield, medical history will be confirmed by chart review. The Marshfield cohort is 98% white American and 57% female with a mean age of 47.2 years.
collegamento
Keywords
versioni (3)
- 21/07/22 21/07/22 - Simon Heim
- 12/10/22 12/10/22 - Adrian Schulz
- 29/01/25 29/01/25 - Akane Nishihara
Titolare del copyright
Nancy Brown, MD, Vanderbilt University Medical Center, Nashville, TN, USA
Caricato su
12 ottobre 2022
DOI
Per favore, per richiedere un accesso.
Licenza
Creative Commons BY 4.0
Commenti del modello :
Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.
Commenti del gruppo di articoli per :
Commenti dell'articolo per :
Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.
dbGaP phs000438 PGRN-RIKEN: Identification of Genetic Predictors of ACE Inhibitor-Associated Angioedema
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- Subject ID, consent group, and affection status of participants with or without angioedema and involved in the "A Genome-Wide Association Analysis in Angiotensin-Converting enzyme (ACE) Inhibitor-Associated Angioedema and ACE Inhibitor-Exposed Controls; A Collaboration between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Center for Genomic Medicine" project.
- Subject ID, sample ID, and sample use of participants with or without angioedema and involved in the "A Genome-Wide Association Analysis in Angiotensin-Converting enzyme (ACE) Inhibitor-Associated Angioedema and ACE Inhibitor-Exposed Controls; A Collaboration between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Center for Genomic Medicine" project.
- Subject ID, case or control, age, gender, and race of participants with or without angioedema and involved in the "A Genome-Wide Association Analysis in Angiotensin-Converting enzyme (ACE) Inhibitor-Associated Angioedema and ACE Inhibitor-Exposed Controls; A Collaboration between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Center for Genomic Medicine" project.
- Sample ID, body site where sample was collected of participants with or without angioedema and involved in the "A Genome-Wide Association Analysis in Angiotensin-Converting enzyme (ACE) Inhibitor-Associated Angioedema and ACE Inhibitor-Exposed Controls; A Collaboration between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Center for Genomic Medicine" project.
Similar models
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- Subject ID, consent group, and affection status of participants with or without angioedema and involved in the "A Genome-Wide Association Analysis in Angiotensin-Converting enzyme (ACE) Inhibitor-Associated Angioedema and ACE Inhibitor-Exposed Controls; A Collaboration between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Center for Genomic Medicine" project.
- Subject ID, sample ID, and sample use of participants with or without angioedema and involved in the "A Genome-Wide Association Analysis in Angiotensin-Converting enzyme (ACE) Inhibitor-Associated Angioedema and ACE Inhibitor-Exposed Controls; A Collaboration between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Center for Genomic Medicine" project.
- Subject ID, case or control, age, gender, and race of participants with or without angioedema and involved in the "A Genome-Wide Association Analysis in Angiotensin-Converting enzyme (ACE) Inhibitor-Associated Angioedema and ACE Inhibitor-Exposed Controls; A Collaboration between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Center for Genomic Medicine" project.
- Sample ID, body site where sample was collected of participants with or without angioedema and involved in the "A Genome-Wide Association Analysis in Angiotensin-Converting enzyme (ACE) Inhibitor-Associated Angioedema and ACE Inhibitor-Exposed Controls; A Collaboration between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Center for Genomic Medicine" project.
C1706256 (UMLS CUI [1,2])
C0001779 (UMLS CUI [1,3])
C1512693 (UMLS CUI [2,1])
C1706256 (UMLS CUI [2,2])
C0085756 (UMLS CUI [2,3])
C0221786 (UMLS CUI [2,4])
C1512693 (UMLS CUI [3,1])
C1706256 (UMLS CUI [3,2])
C0002994 (UMLS CUI [3,3])
C0003015 (UMLS CUI [3,4])
C0009932 (UMLS CUI [1,2])
C0001779 (UMLS CUI [1,3])
C1512693 (UMLS CUI [2,1])
C0009932 (UMLS CUI [2,2])
C0085756 (UMLS CUI [2,3])
C0221786 (UMLS CUI [2,4])
C1512693 (UMLS CUI [3,1])
C0009932 (UMLS CUI [3,2])
C0003015 (UMLS CUI [3,3])
C4082120 (UMLS CUI [3,4])
C2003901 (UMLS CUI [3,5])
C0002994 (UMLS CUI [3,6])
C1512693 (UMLS CUI [4,1])
C0009932 (UMLS CUI [4,2])
C0010200 (UMLS CUI [4,3])
C0002994 (UMLS CUI [1,2])
C0003015 (UMLS CUI [1,3])
C0680251 (UMLS CUI [2,1])
C3888796 (UMLS CUI [2,2])
C0680251 (UMLS CUI [3,1])
C0205216 (UMLS CUI [3,2])
C0540301 (UMLS CUI [3,3])
C0009498 (UMLS CUI [3,4])
C0680251 (UMLS CUI [4,1])
C3841804 (UMLS CUI [4,2])