Evidence map›Paper›PMID 40510603›Full record

ArticleKidney medicine2025

Utilization Trends of Dual GIP/GLP-1 Receptor Agonist, Newer Glucose-Lowering Medications, and Anti-Obesity Medications Among Patients With Chronic Kidney Disease With and Without Type 2 Diabetes.

Panupong Hansrivijit, Janinne Ortega-Montiel, Deborah J Wexler, Elisabetta Patorno, Julie M Paik

Abstract read
In one paragraph

Article in Kidney medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Panupong HansrivijitDivision of Pharmacoepidemiology & Pharmacoeconomics, Brigham and Women's Hospital, Boston, MA.
Janinne Ortega-MontielDivision of Pharmacoepidemiology & Pharmacoeconomics, Brigham and Women's Hospital, Boston, MA.
Deborah J WexlerDiabetes Center, Massachusetts General Hospital, Boston, MA.
Elisabetta PatornoDivision of Pharmacoepidemiology & Pharmacoeconomics, Brigham and Women's Hospital, Boston, MA.
Julie M PaikDivision of Pharmacoepidemiology & Pharmacoeconomics, Brigham and Women's Hospital, Boston, MA.

Funding

Novel approaches to improve comparative effectiveness research of medical and surgical weight reduction strategies in clinical practiceR01DK138036 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI Elisabetta Patorno · 2024 to 2026
$2.3M
Optimizing the Safety of the Newer Diabetes Medications in Patients with Diabetes and Kidney DiseaseR01DK135706 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI Julie M Paik · 2024 to 2026
$2.2M
NIDDK NIH HHS R01 DK135706NIDDK NIH HHS R01 DK138036
6 · The paper itself

Abstract

Rationale & Objective: Tirzepatide, a dual GIP/GLP-1 receptor agonist, has been approved for type 2 diabetes (T2D) and obesity. However, the real-world utilization of tirzepatide remains unexplored, particularly in patients with chronic kidney disease (CKD), where the prevalence of T2D and obesity is high. This study aimed to describe the utilization trends of tirzepatide, glucose-lowering medications (GLMs), and anti-obesity medications (AOMs) in patients with CKD, with and without T2D. Study Design: A population-based, observational cohort study. Setting & Participants: Patients with CKD, with and without T2D, were identified from a large US health insurance claims database (from January 1, 2022 to September 30, 2023). Exposures: Tirzepatide, other GLMs, and AOMs. Outcomes: Medication utilization trends and patient characteristics. Any users were defined as those with prescription claims, and incident users as those with no previous dispensing within 365 days. Analytical Approach: Longitudinal trends were assessed by 1-month intervals from January 1, 2022 to September 30, 2023. Results: Among 455,047 patients with CKD and T2D, tirzepatide any users increased to 4.8% in September 2023, while incident users rose from 0.8% to 8.6%. Sodium glucose cotransporter-2 inhibitors remained the most initiated GLM. Tirzepatide initiators had higher rates of obesity (32.5%), and morbid obesity (44.1%) when compared with other GLMs. Among 5,978 patients with CKD without diabetes, weekly semaglutide ≤2 mg was the most initiated AOM, followed by tirzepatide. Incident users of tirzepatide rose from 0.6% in June 2022 to 23.5% in September 2023. Clinical characteristics were similar between semaglutide ≤2 mg versus tirzepatide initiators. Limitations: The study period ended before tirzepatide's approval for weight management (November 2023). Conclusions: Our study indicates rapidly shifting trends in tirzepatide uptake among patients with CKD both with and without diabetes. The uptake of tirzepatide is expected to increase further. Future studies on the comparative effectiveness and safety of tirzepatide in patients with CKD are warranted.

Indexed as

adult obesitychronic kidney diseaseGIP/GLP-1GLP-1 receptor agonistsprescribing trendsSGLT2 inhibitorstype 2 diabetes

Identifiers

PMID40510603
PMCPMC12152630

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.