ID

45622

Beskrivning

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.

Länk

dbGaP study = phs001350

Nyckelord

  1. 2023-02-27 2023-02-27 - Simon Heim
Rättsinnehavare

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

Uppladdad den

27 februari 2023

DOI

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Licens

Creative Commons BY 4.0

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

Eligibility Criteria

Inclusion and exclusion criteria
Beskrivning

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
Inclusion/exclusion was based on enrollment on the clinical trials of ALL at St. Jude Children's Research Hospital and the Children's Oncology Group, informed consent following OPRR guidelines, availability of germline DNA, and data quality in subsequent genotyping experiments.
Beskrivning

Inclusion/exclusion was based on enrollment on the clinical trials of ALL at St. Jude Children's Research Hospital and the Children's Oncology Group, informed consent following OPRR guidelines, availability of germline DNA, and data quality in subsequent genotyping experiments.

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0441833
UMLS CUI [1,2]
C1512693
UMLS CUI [1,3]
C0680251
UMLS CUI [1,4]
C1516879
UMLS CUI [1,5]
C0008976
UMLS CUI [1,6]
C0023449
UMLS CUI [1,7]
C1519168
UMLS CUI [1,8]
C1516477
UMLS CUI [1,9]
C0021430
UMLS CUI [1,10]
C0162791
UMLS CUI [1,11]
C2986526
UMLS CUI [1,12]
C0242483
UMLS CUI [1,13]
C1285573

Similar models

Eligibility Criteria

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Inclusion/exclusion was based on enrollment on the clinical trials of ALL at St. Jude Children's Research Hospital and the Children's Oncology Group, informed consent following OPRR guidelines, availability of germline DNA, and data quality in subsequent genotyping experiments.
Item
Inclusion/exclusion was based on enrollment on the clinical trials of ALL at St. Jude Children's Research Hospital and the Children's Oncology Group, informed consent following OPRR guidelines, availability of germline DNA, and data quality in subsequent genotyping experiments.
boolean
C0441833 (UMLS CUI [1,1])
C1512693 (UMLS CUI [1,2])
C0680251 (UMLS CUI [1,3])
C1516879 (UMLS CUI [1,4])
C0008976 (UMLS CUI [1,5])
C0023449 (UMLS CUI [1,6])
C1519168 (UMLS CUI [1,7])
C1516477 (UMLS CUI [1,8])
C0021430 (UMLS CUI [1,9])
C0162791 (UMLS CUI [1,10])
C2986526 (UMLS CUI [1,11])
C0242483 (UMLS CUI [1,12])
C1285573 (UMLS CUI [1,13])

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