ID

45622

Beschreibung

Principal Investigator: Mary V. Relling, PharmD, St. Jude Children's Research Hospital MeSH: Leukemia, Lymphoid,Pancreatitis https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001350 A complication of acute lymphoblastic leukemia (ALL) treatment is acute pancreatitis, which is one of the common causes of asparaginase intolerance. To determine clinical and genetic risk factors for pancreatitis, we studied a cohort of children and young adults with ALL enrolled on COG trials (9904/9905/9906, AALL0232) and on St. Jude trial Total XV. We performed a genome-wide association study using germline DNA collected from blood in patients at remission in this cohort of 5185 patients and in an independent case-control group of 213 patients on AALL0331. The frequency of pancreatitis in the cohort was 2.3% (117 of 5185). No common variants reached genome-wide significance, but a rare nonsense variant rs199695765 in CPA2, encoding carboxypeptidase A2, was highly associated with pancreatitis (odds ratio = 587, 95% confidence interval 66.8-5166, P = 9.0 x 10-9). A gene-level analysis showed an excess of additional CPA2 variants in patients who did versus those who did not develop pancreatitis (P = 0.018). Sixteen CPA2 SNPs were associated (P 0.05) with pancreatitis, and 13 of 24 patients who carried at least one of these variants developed pancreatitis. Biological functions that were overrepresented by common variants modestly associated with pancreatitis included purine metabolism and cytoskeleton regulation.

Link

dbGaP study = phs001350

Stichworte

  1. 27.02.23 27.02.23 - Simon Heim
Rechteinhaber

Mary V. Relling, PharmD, St. Jude Children's Research Hospital

Hochgeladen am

27. Februar 2023

DOI

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Lizenz

Creative Commons BY 4.0

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dbGaP phs001350 Pancreatitis after Treatment for Acute Lymphoblastic Leukemia (SJIRB XPD04-123 and XPD05-078)

Subject ID, St Jude TOTALXV protocols, with or without pancreatitis, gender, and genotype race of participants with or without pancreatitis and involved in the "Pancreatitis after Treatment for Acute Lymphoblastic Leukemia (SJIRB XPD04-123 and XPD05-078)" project.

pht009879
Beschreibung

pht009879

Alias
UMLS CUI [1,1]
C3846158
De-identified subject identifier
Beschreibung

N/A

Datentyp

string

Alias
UMLS CUI [1,1]
C4684638
UMLS CUI [1,2]
C2348585
St Jude TOTALXV protocols; Children's Oncology Group P9904, P9905, P9906, AALL0331 and AALL0232 protocols.
Beschreibung

N/A

Datentyp

string

Alias
UMLS CUI [1,1]
C4683627
UMLS CUI [1,2]
C1516477
1 indicates pancreatitis, 0 not so
Beschreibung

N/A

Datentyp

string

Alias
UMLS CUI [1,1]
C1522602
UMLS CUI [1,2]
C0030305
Gender [Male or Female]
Beschreibung

N/A

Datentyp

string

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C0086582
UMLS CUI [1,3]
C0086287
Race genetically determined using STRUCTURE with genome-wide mapping array
Beschreibung

N/A

Datentyp

string

Alias
UMLS CUI [1,1]
C0034510
UMLS CUI [1,2]
C0079435
UMLS CUI [1,3]
C0678594

Ähnliche Modelle

Subject ID, St Jude TOTALXV protocols, with or without pancreatitis, gender, and genotype race of participants with or without pancreatitis and involved in the "Pancreatitis after Treatment for Acute Lymphoblastic Leukemia (SJIRB XPD04-123 and XPD05-078)" project.

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
pht009879
C3846158 (UMLS CUI [1,1])
SUBJECT_ID
Item
De-identified subject identifier
string
C4684638 (UMLS CUI [1,1])
C2348585 (UMLS CUI [1,2])
Clinical_Protocol
Item
St Jude TOTALXV protocols; Children's Oncology Group P9904, P9905, P9906, AALL0331 and AALL0232 protocols.
string
C4683627 (UMLS CUI [1,1])
C1516477 (UMLS CUI [1,2])
Pancreatitis
Item
1 indicates pancreatitis, 0 not so
string
C1522602 (UMLS CUI [1,1])
C0030305 (UMLS CUI [1,2])
Gender
Item
Gender [Male or Female]
string
C0079399 (UMLS CUI [1,1])
C0086582 (UMLS CUI [1,2])
C0086287 (UMLS CUI [1,3])
GenotypeRace
Item
Race genetically determined using STRUCTURE with genome-wide mapping array
string
C0034510 (UMLS CUI [1,1])
C0079435 (UMLS CUI [1,2])
C0678594 (UMLS CUI [1,3])

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