GLP1R Gene Expression and Kidney Disease Progression.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
01 Oct 2024
Historique:
medline: 25 10 2024
pubmed: 25 10 2024
entrez: 25 10 2024
Statut: epublish

Résumé

Glucagon-like peptide 1 receptor agonists (GLP-1RAs) may have nephroprotective properties beyond those related to weight loss and glycemic control. To investigate the association of genetically proxied GLP-1RAs with kidney disease progression. This genetic association study assembled a national retrospective cohort of veterans aged 18 years or older from the US Department of Veterans Affairs Million Veteran Program between January 10, 2011, and December 31, 2021. Data were analyzed from November 2023 to February 2024. Genetic risk score for systemic GLP1R gene expression that was calculated for each study participant based on genetic variants associated with GLP1R mRNA levels across all tissue samples within the Genotype-Tissue Expression project. The primary composite outcome was incident end-stage kidney disease or a 40% decline in estimated glomerular filtration rate. Cox proportional hazards regression survival analysis assessed the association between genetically proxied GLP-1RAs and kidney disease progression. Among 353 153 individuals (92.5% men), median age was 66 years (IQR, 58.0-72.0 years) and median follow-up was 5.1 years (IQR, 3.1-7.2 years). Overall, 25.7% had diabetes, and 45.0% had obesity. A total of 4.6% experienced kidney disease progression. Overall, higher genetic GLP1R gene expression was associated with a lower risk of kidney disease progression in the unadjusted model (hazard ratio [HR], 0.96; 95% CI, 0.92-0.99; P = .02) and in the fully adjusted model accounting for baseline patient characteristics, body mass index, and the presence or absence of diabetes (HR, 0.96; 95% CI, 0.92-1.00; P = .04). The results were similar in sensitivity analyses stratified by diabetes or obesity status. In this genetic association study, higher GLP1R gene expression was associated with a small reduction in risk of kidney disease progression. These findings support pleiotropic nephroprotective mechanisms of GLP-1RAs independent of their effects on body weight and glycemic control.

Identifiants

pubmed: 39453656
pii: 2825345
doi: 10.1001/jamanetworkopen.2024.40286
doi:

Substances chimiques

Glucagon-Like Peptide-1 Receptor 0
GLP1R protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2440286

Investigateurs

Sumitra Muralidhar (S)
Jennifer Moser (J)
Jennifer E Deen (JE)
Philip S Tsao (PS)
J Michael Gaziano (JM)
Elizabeth Hauser (E)
Amy Kilbourne (A)
Michael Matheny (M)
Dave Oslin (D)
Lori Churby (L)
Stacey B Whitbourne (SB)
Jessica V Brewer (JV)
Shahpoor Alex Shayan (SA)
Luis E Selva (LE)
Saiju Pyarajan (S)
Kelly Cho (K)
Scott L DuVall (SL)
Mary T Brophy (MT)
Brady Stephens (B)
Todd Connor (T)
Dean P Argyres (DP)
Tim Assimes (T)
Adriana Hung (A)
Henry Kranzler (H)
Samuel Aguayo (S)
Sunil Ahuja (S)
Kathrina Alexander (K)
Xiao M Androulakis (XM)
Prakash Balasubramanian (P)
Zuhair Ballas (Z)
Jean Beckham (J)
Sujata Bhushan (S)
Edward Boyko (E)
David Cohen (D)
Louis Dellitalia (L)
L Christine Faulk (LC)
Joseph Fayad (J)
Daryl Fujii (D)
Saib Gappy (S)
Frank Gesek (F)
Jennifer Greco (J)
Michael Godschalk (M)
Todd W Gress (TW)
Samir Gupta (S)
Salvador Gutierrez (S)
John Harley (J)
Mark Hamner (M)
Robin Hurley (R)
Pran Iruvanti (P)
Frank Jacono (F)
Darshana Jhala (D)
Scott Kinlay (S)
Michael Landry (M)
Peter Liang (P)
Suthat Liangpunsakul (S)
Jack Lichy (J)
C Scott Mahan (CS)
Ronnie Marrache (R)
Stephen Mastorides (S)
Kristin Mattocks (K)
Paul Meyer (P)
Jonathan Moorman (J)
Timothy Morgan (T)
Maureen Murdoch (M)
James Norton (J)
Olaoluwa Okusaga (O)
Kris Ann Oursler (KA)
Samuel Poon (S)
Michael Rauchman (M)
Richard Servatius (R)
Satish Sharma (S)
River Smith (R)
Peruvemba Sriram (P)
Patrick Strollo (P)
Neeraj Tandon (N)
Gerardo Villareal (G)
Jessica Walsh (J)
John Wells (J)
Jeffrey Whittle (J)
Mary Whooley (M)
Peter Wilson (P)
Junzhe Xu (J)
Shing Shing Yeh (SS)
Elizabeth S Bast (ES)
Gerald Wayne Dryden (GW)
Daniel J Hogan (DJ)
Seema Joshi (S)
Tze Shien Lo (TS)
Providencia Morales (P)
Eknath Naik (E)
Michael K Ong (MK)
Ismene Petrakis (I)
Amneet S Rai (AS)
Andrew W Yen (AW)

Auteurs

Jefferson L Triozzi (JL)

Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.

Zhihong Yu (Z)

Department of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.

Ayush Giri (A)

Division of Quantitative Sciences, Department of Obstetrics and Gynecology, Vanderbilt University, Nashville, Tennessee.
Division of Epidemiology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.

Hua-Chang Chen (HC)

Department of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.

Otis D Wilson (OD)

Nashville VA Medical Center, VA Tennessee Valley Healthcare System, Nashville.

Brian Ferolito (B)

Million Veteran Program Coordinating Center, VA Boston Healthcare System, Boston, Massachusetts.

T Alp Ikizler (TA)

Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.

Elvis A Akwo (EA)

Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.

Cassianne Robinson-Cohen (C)

Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.

John Michael Gaziano (JM)

Million Veteran Program Coordinating Center, VA Boston Healthcare System, Boston, Massachusetts.
Department of Medicine, Brigham and Women's Hospital and Harvard School of Medicine, Boston, Massachusetts.

Kelly Cho (K)

Million Veteran Program Coordinating Center, VA Boston Healthcare System, Boston, Massachusetts.
Department of Medicine, Brigham and Women's Hospital and Harvard School of Medicine, Boston, Massachusetts.

Lawrence S Phillips (LS)

VA Atlanta Health Care System, Decatur, Georgia.
Division of Endocrinology and Metabolism, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia.

Ran Tao (R)

Department of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.
Vanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville, Tennessee.

Alexandre C Pereira (AC)

Million Veteran Program Coordinating Center, VA Boston Healthcare System, Boston, Massachusetts.
Department of Medicine, Brigham and Women's Hospital and Harvard School of Medicine, Boston, Massachusetts.

Adriana M Hung (AM)

Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Nashville VA Medical Center, VA Tennessee Valley Healthcare System, Nashville.

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