TY - JOUR
T1 - Real-World Clinical Practice Among Patients With Bipolar Disorder and Chronic Kidney Disease on Long-term Lithium Therapy
AU - Kumar, Rakesh
AU - Joseph, Boney
AU - Pazdernik, Vanessa M.
AU - Geske, Jennifer
AU - Nuñez, Nicolas A.
AU - Pahwa, Mehak
AU - Kashani, Kianoush B.
AU - Veldic, Marin
AU - Betcher, Hannah K.
AU - Moore, Katherine M.
AU - Croarkin, Paul E.
AU - Ozerdem, Aysegul
AU - Cuellar-Barboza, Alfredo B.
AU - McElroy, Susan L.
AU - Biernacka, Joanna M.
AU - Frye, Mark A.
AU - Singh, Balwinder
N1 - Funding Information:
Nicolas A. Nuñez reports research support by the National Institute of General Medical Sciences of the National Institutes of Health under award number T32 GM008685. Paul E. Croarkin has received research support from Neuronetics, Inc; NeoSync, Inc; and Pfizer. He has received grant in kind (equipment and laboratory support for research studies) from Assurex Health; Neuronetics, Inc; and MagVenture, Inc. He has served as a consultant for Engrail Therapeutics, Myriad Neuroscience, Procter & Gamble, and Sunovion. Balwinder Singh received grant support from Mayo Clinic. Susan L. McElroy is or has been a consultant to or member of the scientific advisory boards of Avanir; Allergan (now AbbVie); Bracket (now Signant Health); Naurex; Idorsia; Intra-Cellular Therapies, Inc; Shire (now Takeda); Sunovion; and Takeda. She is or has been a principal or coinvestigator on studies sponsored by the Agency for Healthcare Research & Quality; Avenir; AstraZeneca; Cephalon; Forest; Marriott Foundation; Medibio; National Institute of Mental Health; Orexigen Therapeutics, Inc; Jazz; Shire (now Takeda); Sunovian; and Takeda Pharmaceutical Company Ltd. She is also an inventor on United States Patent No. 6,323,236 B2, Use of Sulfamate Derivatives for Treating Impulse Control Disorders, and along with the patent's assignee, the University of Cincinnati, Cincinnati, Ohio, has received payments from Johnson & Johnson, which has exclusive rights under the patent. Mark A. Frye received support from Assurex Health, Mayo Foundation, and Medibio. The remaining authors declare no conflicts of interest. This research was supported by the Marriott Family Foundation.
Publisher Copyright:
Copyright © 2022 Wolters Kluwer Health, Inc. All rights reserved.
PY - 2023/1/1
Y1 - 2023/1/1
N2 - Purpose: Long-term lithium therapy (LTLT) has been associated with chronic kidney disease (CKD). We investigated changes in clinical characteristics, pharmacotherapeutic treatments for medical/psychiatric disorders, and outcomes among patients with bipolar disorder (BD) and CKD on LTLT in a 2-year mirror-image study design. Methods: Adult BD patients on LTLT for ≥1 year who enrolled in the Mayo Clinic Bipolar Disorder Biobank and developed CKD (stage 3) were included, and our study was approved by the Mayo Clinic Institutional Review Board. The primary outcome was the time to the first mood episode after CKD diagnosis among the lithium (Li) continuers and discontinuers. Cox proportional hazards models were used to estimate the time to the first mood episode. We tested for differences in other medication changes between the Li continuers and discontinuers group using Mantel-Haenszel χ2 tests (linear associations). Results: Of 38 BD patients who developed CKD, 18 (47%) discontinued Li, and the remainder continued (n = 20). The median age of the cohort was 56 years (interquartile range [IQR], 48–67 years), 63.2% were female, and 97.4% were White. As compared with continuers, discontinuers had more psychotropic medication trials (6 [IQR, 4–6] vs 3 [IQR, 2–5], P = 0.02), a higher rate of 1 or more mood episodes (61% vs 10%, P = 0.002), and a higher risk of a mood episode after CKD diagnoses (Hazard Ratio, 8.38; 95% confidence interval, 1.85–38.0 [log-rank P = 0.001]]. Conclusions: Bipolar disorder patients on LTLT who discontinued Li had a higher risk for relapse and a shorter time to the first mood episode, suggesting a need for more thorough discussion before Li discontinuation after the CKD diagnosis.
AB - Purpose: Long-term lithium therapy (LTLT) has been associated with chronic kidney disease (CKD). We investigated changes in clinical characteristics, pharmacotherapeutic treatments for medical/psychiatric disorders, and outcomes among patients with bipolar disorder (BD) and CKD on LTLT in a 2-year mirror-image study design. Methods: Adult BD patients on LTLT for ≥1 year who enrolled in the Mayo Clinic Bipolar Disorder Biobank and developed CKD (stage 3) were included, and our study was approved by the Mayo Clinic Institutional Review Board. The primary outcome was the time to the first mood episode after CKD diagnosis among the lithium (Li) continuers and discontinuers. Cox proportional hazards models were used to estimate the time to the first mood episode. We tested for differences in other medication changes between the Li continuers and discontinuers group using Mantel-Haenszel χ2 tests (linear associations). Results: Of 38 BD patients who developed CKD, 18 (47%) discontinued Li, and the remainder continued (n = 20). The median age of the cohort was 56 years (interquartile range [IQR], 48–67 years), 63.2% were female, and 97.4% were White. As compared with continuers, discontinuers had more psychotropic medication trials (6 [IQR, 4–6] vs 3 [IQR, 2–5], P = 0.02), a higher rate of 1 or more mood episodes (61% vs 10%, P = 0.002), and a higher risk of a mood episode after CKD diagnoses (Hazard Ratio, 8.38; 95% confidence interval, 1.85–38.0 [log-rank P = 0.001]]. Conclusions: Bipolar disorder patients on LTLT who discontinued Li had a higher risk for relapse and a shorter time to the first mood episode, suggesting a need for more thorough discussion before Li discontinuation after the CKD diagnosis.
KW - bipolar disorders
KW - chronic kidney disease
KW - lithium
KW - mirror-image study
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U2 - 10.1097/JCP.0000000000001632
DO - 10.1097/JCP.0000000000001632
M3 - Article
C2 - 36584244
AN - SCOPUS:85145425777
VL - 43
SP - 6
EP - 11
JO - Journal of Clinical Psychopharmacology
JF - Journal of Clinical Psychopharmacology
SN - 0271-0749
IS - 1
ER -