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GWAS Study

Novel genetic susceptibility loci for diabetic end-stage renal disease identified through robust naive Bayes classification.

Sambo F, Malovini A, Sandholm N et al.

24871321 PubMed ID
GWAS Study Type
7727 Participants
78 Views
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SF
Sambo F
MA
Malovini A
SN
Sandholm N
SM
Stavarachi M
FC
Forsblom C
MV
Mäkinen VP
HV
Harjutsalo V
LR
Lithovius R
GD
Gordin D
PM
Parkkonen M
SM
Saraheimo M
TL
Thorn LM
TN
Tolonen N
WJ
Wadén J
HB
He B
OA
Osterholm AM
TJ
Tuomilehto J
LM
Lajer M
SR
Salem RM
MA
McKnight AJ
TL
Tarnow L
PN
Panduru NM
BN
Barbarini N
DC
Di Camillo B
TG
Toffolo GM
TK
Tryggvason K
BR
Bellazzi R
CC
Cobelli C
GP
Groop PH
Chapter II

Abstract

Summary of the research findings

Aims/hypothesis: Diabetic nephropathy is a major diabetic complication, and diabetes is the leading cause of end-stage renal disease (ESRD). Family studies suggest a hereditary component for diabetic nephropathy. However, only a few genes have been associated with diabetic nephropathy or ESRD in diabetic patients. Our aim was to detect novel genetic variants associated with diabetic nephropathy and ESRD.

661 European ancestry End-stage renal disease cases, 694 European ancestry Diabetic nephropathy cases, 472 European ancestry Microalbuminuria cases, 1,637 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

7727
Total Participants
GWAS
Study Type
Yes
Replicated
92 End-stage renal disease cases, 345 Diabetic nephropathy cases, 135 Microalbuminuria cases, 370 controls
Replication Participants
European, NR, European
Ancestry
Finland, U.S., U.K., Republic of Ireland, Denmark
Recruitment Country
Chapter IV

AI-Generated Summary

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