Menu
Currency
GWAS Study

Genetics of 35 blood and urine biomarkers in the UK Biobank.

Sinnott-Armstrong N, Tanigawa Y, Amar D et al.

33462484 PubMed ID
GWAS Study Type
345182 Participants
243 Views
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SN
Sinnott-Armstrong N
TY
Tanigawa Y
AD
Amar D
MN
Mars N
BC
Benner C
AM
Aguirre M
VG
Venkataraman GR
WM
Wainberg M
OH
Ollila HM
KT
Kiiskinen T
HA
Havulinna AS
PJ
Pirruccello JP
QJ
Qian J
SA
Shcherbina A
RF
Rodriguez F
AT
Assimes TL
AV
Agarwala V
TR
Tibshirani R
HT
Hastie T
RS
Ripatti S
PJ
Pritchard JK
DM
Daly MJ
RM
Rivas MA
Chapter II

Abstract

Summary of the research findings

Clinical laboratory tests are a critical component of the continuum of care. We evaluate the genetic basis of 35 blood and urine laboratory measurements in the UK Biobank (n = 363,228 individuals). We identify 1,857 loci associated with at least one trait, containing 3,374 fine-mapped associations and additional sets of large-effect (>0.1 s.d.) protein-altering, human leukocyte antigen (HLA) and copy number variant (CNV) associations. Through Mendelian randomization (MR) analysis, we discover 51 causal relationships, including previously known agonistic effects of urate on gout and cystatin C on stroke. Finally, we develop polygenic risk scores (PRSs) for each biomarker and build 'multi-PRS' models for diseases using 35 PRSs simultaneously, which improved chronic kidney disease, type 2 diabetes, gout and alcoholic cirrhosis genetic risk stratification in an independent dataset (FinnGen; n = 135,500) relative to single-disease PRSs. Together, our results delineate the genetic basis of biomarkers and their causal influences on diseases and improve genetic risk stratification for common diseases.

332,398 European ancestry individuals, 5,786 African ancestry individuals, 6,998 South Asian ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

345182
Total Participants
GWAS
Study Type
No
Replicated
European, African unspecified, South Asian
Ancestry
Chapter IV

AI-Generated Summary

AI-generated by DNAGENICS

Independent AI summary of health and genetic findings from the published study

Important: This summary is AI-generated by DNAGENICS for informational purposes only. It was not created by, affiliated with, or endorsed by the researchers behind the original publication, and is based solely on that published research. It may contain errors or omissions. DNAGENICS disclaims all liability for any inaccuracies or consequences arising from use of this information. Verify all information against the original publication. This is not professional scientific review or medical advice.

AI Summary In Progress

Our AI-generated summary of this publication is being prepared. Please check back soon.