Genetic Epidemiology, Translational Neurogenomics, Psychiatric Genetics and Statistical Genetics Laboratories investigate the pattern of disease in families, particularly identical and non-identical twins, to assess the relative importance of genes and environment in a variety of important health problems.
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PMID
41951734
TITLE
Genetic predictors of GLP1 receptor agonist weight loss and side effects.
ABSTRACT
The development of glucagon-like peptide 1 (GLP1) receptor agonists, including semaglutide and tirzepatide, has transformed the clinical management of overweight and obesity. However, substantial inter-person variability exists in both weight loss efficacy and the incidence of side effects . To investigate the genetic basis of this variability, here we conduct a genome-wide association study of self-reported weight loss and treatment-related side effects in 27,885 people following GLP1 receptor agonist therapy. We identify a missense variant in GLP1R that is associated significantly with increased efficacy of GLP1 medications (P = 2.9 × 10 ), with an additional -0.76 kg of weight loss expected per copy of the effect allele. Furthermore, we identify associations linking variation in both GLP1R and GIPR to GLP1 medication-related nausea or vomiting, with the GIPR association being restricted to people using tirzepatide. We incorporate these findings into a broader model of GLP1 medication response, and demonstrate the ability to stratify patients by efficacy and side effect risk. These findings provide direct genetic evidence that variation in the drug target genes contributes to inter-person variability in response and lay the foundation for precision medicine approaches in the treatment of obesity.
© 2026. The Author(s).
DATE PUBLISHED
2026 May
HISTORY
PUBSTATUS PUBSTATUSDATE
received 2025/10/02
accepted 2026/02/26
medline 2026/05/21 06:31
pubmed 2026/04/09 00:34
entrez 2026/04/08 23:21
pmc-release 2026/04/08
AUTHORS
NAME COLLECTIVENAME LASTNAME FORENAME INITIALS AFFILIATION AFFILIATIONINFO
Su QJ Su Qiaojuan Jane QJ 23andMe Research Institute, Palo Alto, CA, USA.
Ashenhurst JR Ashenhurst James R JR 23andMe Research Institute, Palo Alto, CA, USA.
Xu W Xu Wanwan W 23andMe Research Institute, Palo Alto, CA, USA.
Tran V Tran Vinh V 23andMe Research Institute, Palo Alto, CA, USA.
Ryanne Wu R Ryanne Wu R R 23andMe Research Institute, Palo Alto, CA, USA.
Weldon CH Weldon Catherine H CH 23andMe Research Institute, Palo Alto, CA, USA.
Shi J Shi Jingchunzi J 23andMe Research Institute, Palo Alto, CA, USA.
Hicks B Hicks Barry B 23andMe Research Institute, Palo Alto, CA, USA.
23andMe Research Team
Abul-Husn NS Abul-Husn Noura S NS 23andMe Research Institute, Palo Alto, CA, USA.
Aslibekyan S Aslibekyan Stella S 23andMe Research Institute, Palo Alto, CA, USA.
Holmes MV Holmes Michael V MV 23andMe Research Institute, Palo Alto, CA, USA.
Koelsch BL Koelsch Bertram L BL 23andMe Research Institute, Palo Alto, CA, USA.
Auton A Auton Adam A 23andMe Research Institute, Palo Alto, CA, USA. aauton@23andme.com.
INVESTIGATORS
LASTNAME FORENAME INITIALS AFFILIATION
Bell Robert K RK
Bond Katelyn Kukar KK
Cochinwala Zayn Z
Das Sayantan S
de Brito Kahsaia K
Dhamija Devika D
Dibaeinia Payambr P
DelloRusso Emily E
Eijsbouts Chris C
Elson Sarah L SL
Fuller Shirin S
German Chris C
Granka Julie M JM
Hengl Larry L
Hinds David A DA
Jabal Reza R
Khan Aly A
Kmiecik Matthew J MJ
Kwong Alan A
Liang Yanyu Y
Lin Keng-Han KH
McIntyre Matthew H MH
Moran Alex A
Northover Carrie C
Saini Shubham S
Shastri Anjali J AJ
Shringarpure Suyash S
Sterling Teague T
Tung Joyce Y JY
JOURNAL
VOLUME: 653
ISSUE: 8115
TITLE: Nature
ISOABBREVIATION: Nature
YEAR: 2026
MONTH: May
DAY:
MEDLINEDATE:
SEASON:
CITEDMEDIUM: Internet
ISSN: 1476-4687
ISSNTYPE: Electronic
MEDLINE JOURNAL
MEDLINETA: Nature
COUNTRY: England
ISSNLINKING: 0028-0836
NLMUNIQUEID: 0410462
PUBLICATION TYPE
PUBLICATIONTYPE TEXT
Journal Article
COMMENTS AND CORRECTIONS
GRANTS
GENERAL NOTE
KEYWORDS
MESH HEADINGS
DESCRIPTORNAME QUALIFIERNAME
Adult
Female
Humans
Male
Middle Aged
Alleles
Genome-Wide Association Study
Glucagon-Like Peptide-1 Receptor genetics
Glucagon-Like Peptide-1 Receptor Agonists therapeutic use
Glucagon-Like Peptides adverse effects
Mutation, Missense genetics
Nausea chemically induced
Obesity genetics
Receptors, Gastrointestinal Hormone genetics
Tirzepatide genetics
Treatment Outcome genetics
Weight Loss drug effects
SUPPLEMENTARY MESH
GENE SYMBOLS
CHEMICALS
REGISTRYNUMBER NAMEOFSUBSTANCE
D6H00MV7K8 gastric inhibitory polypeptide receptor
0 GLP1R protein, human
0 Glucagon-Like Peptide-1 Receptor
0 Glucagon-Like Peptide-1 Receptor Agonists
62340-29-8 Glucagon-Like Peptides
0 Receptors, Gastrointestinal Hormone
OYN3CCI6QE Tirzepatide
OTHER ID's