JCP Webinar

GLP-1 Receptor Agonists for Long-Term Kidney Protection

In this webinar, Balwinder Singh, MD, and Raman Baweja, MD, describe emerging evidence on GLP-1 receptor agonists for long-term kidney protection in bipolar disorder with chronic kidney disease. They discuss the real-world cohort findings on kidney replacement therapy and lithium monitoring considerations raised during the Q and A.

October 23, 2026

Watch the Video Abstract

Balwinder Singh, MD, and Raman Baweja, MD, describe emerging evidence on GLP-1 receptor agonists, kidney replacement therapy outcomes, and lithium monitoring in bipolar disorder with chronic kidney disease.

JCP Webinar

In this webinar, Balwinder Singh, MD, and Raman Baweja, MD, discuss the role of GLP-1 receptor agonists for long-term kidney protection in bipolar disorder. The presentation begins with the clinical context: lithium remains the gold standard mood stabilizer in bipolar disorder, but concern about chronic kidney disease may contribute to lower prescribing, even though bipolar disorder itself carries substantial cardiometabolic and renal risk.

The speakers then review why chronic kidney disease deserves attention in bipolar disorder, including high rates of obesity, diabetes, and cardiovascular disease, and they summarize kidney-related evidence for GLP-1 receptor agonists. They describe effects in the kidneys, including vasodilatation, action on the afferent and efferent arteriole, lower intraglomerular pressure, and reduced albuminuria, along with indirect effects through glycemic control, weight, insulin resistance, blood pressure, and cardiovascular protection. They also note published cases, case reports, and case series in which starting semaglutide or tirzepatide during lithium treatment was associated with higher lithium levels and toxicity, including one case that required dialysis.

The webinar next covers their real-world cohort analysis in adults aged 18 years and older with bipolar disorder and CKD stages 1, 2, or 3, using a new-user active-comparator design with DPP-4 inhibitors and RAAS inhibitors. The speakers describe propensity score matching, Cox proportional hazards models, Kaplan-Meier analyses, subgroup analyses, and negative controls. They report that GLP-1 receptor agonist use was associated with lower observed hazard of kidney replacement therapy versus both comparator groups, while healthcare utilization findings were less consistent after matching. They close by emphasizing that the findings are hypothesis generating rather than causal and by outlining a cautious lithium monitoring approach when a GLP-1 receptor agonist is started or stopped.

Key Takeaways

  • Lithium is described as the gold standard treatment for bipolar disorder, yet only eleven percent of people with bipolar disorder were said to be prescribed lithium in a paper the speakers published earlier this year.
  • Bipolar disorder is described as carrying a high cardiometabolic burden, with almost fifty percent rates of obesity and two to three times higher rates of diabetes and cardiovascular disease, all of which are risk factors for chronic kidney disease.
  • In the FLOW randomized controlled trial, semaglutide reduced the composite of outcome of kidney failure and kidney and cardiovascular death by twenty-four percent, and semaglutide now has FDA approval for chronic kidney disease.
  • In the speakers' observational cohort, GLP-1 receptor agonist use was associated with lower observed hazard of kidney replacement therapy compared with both DPP-4 inhibitors and RAAS inhibitors, but the speakers emphasize that this is association, not proof for causation.
  • For patients who are stable on lithium and start a newer GLP-1 receptor agonist such as semaglutide or tirzepatide, the transcript advises checking a lithium level before GLP-1 initiation and rechecking after five days, and it states that about fifteen to twenty percent of patients in an ongoing study are having an increase in lithium level.
This is more hypothesis generating. This is the first data suggesting a long-term protection from a kidney standpoint in bipolar and chronic kidney disease, but this is not a randomized controlled trial.

Featured Articles

J Clin Psychiatry 2026;87(4):26m16392

This article describes the real-world cohort analysis discussed in the webinar, comparing GLP-1 receptor agonists with active comparators in adults with bipolar disorder and chronic kidney disease. It is the source of the kidney replacement therapy findings that the speakers frame as hypothesis generating rather than causal.

Read the Study