Comparison of 71 bipolar disorder pharmacotherapies for kidney disorder risk: The potential hazards of polypharmacy

• Published in: Journal of affective disorders Vol. 252; pp. 201 - 211
• Main Authors: Nestsiarovich, Anastasiya, Kerner, Berit, Mazurie, Aurélien J., Cannon, Daniel C., Hurwitz, Nathaniel G., Zhu, Yiliang, Nelson, Stuart J., Oprea, Tudor I., Unruh, Mark L., Crisanti, Annette S., Tohen, Mauricio, Perkins, Douglas J., Lambert, Christophe G.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.06.2019
• Subjects: Adult; Anticonvulsants - adverse effects; Antidepressive Agents - adverse effects; Antimanic Agents - adverse effects; Antipsychotic Agents - adverse effects; Bipolar; Bipolar Disorder - drug therapy; Drug; Female; Humans; Kidney; Kidney Diseases - chemically induced; Male; Middle Aged; Pharmacotherapy; Polypharmacy; Psychiatric; Psychotropic Drugs - adverse effects; Renal; Retrospective Studies; Risk Factors; Drug; Pharmacotherapy; Bipolar; Renal; Kidney; Psychiatric
• ISSN: 0165-0327; 1573-2517
• DOI: 10.1016/j.jad.2019.04.009

•No drug regimen had a significantly lower risk for kidney disorders than “No drug”.•Monoamine oxidase inhibitors had markedly high kidney disorders risk estimates.•Lithium had a 1.27–1.82-fold higher risk of kidney disorders than “No drug”.•Polypharmacy often had higher kidney disorder risk than monotherapy. : This study compared the largest set of bipolar disorder pharmacotherapies to date (71 drugs and drug combinations) for risk of kidney disorders (KDs). : This retrospective observational study used the IBM MarketScan® database to analyze data on 591,052 adults with bipolar disorder without prior nephropathy, for onset of KDs (of “moderate” or “high” severity) following psychopharmacotherapy (lithium, mood stabilizing anticonvulsants [MSAs], antipsychotics, antidepressants), or “No drug”. Cox regression models included fixed pre-treatment covariates and time-varying drug exposure covariates to estimate the hazard ratio (HR) of each treatment versus “No drug”. : Newly observed KD occurred in 14,713 patients. No regimen had significantly lower risk of KDs than “No drug”. The HR estimates ranged 0.86–2.66 for “all” KDs and 0.87–5.30 for “severe” KDs. As additional drugs were combined to compare more complex polypharmacies, higher HRs were consistently observed. Most regimens containing lithium, MSAs, or antipsychotics had a higher risk than “No drug” (p < 0.05). The risk for “all” and “severe” KDs was highest respectively on monoamine oxidase inhibitors (MAOIs) (HR = 2.66, p = 5.73 × 10−5), and a lithium-containing four-class combination (HR = 5.30, p = 2.46 × 10−9). The HR for lithium monotherapy was 1.82 (p = 4.73 × 10−17) for “severe” KDs. : The limitations inherent for an observational study were non-randomized assignment of patients to treatment groups, non-standardization of diagnostic decisions, and non-uniform quality of data collection. No correction was made for medication dosage. : The findings support literature concerns about lithium nephrotoxicity and highlight the potential risks of MAOIs, MSAs, antipsychotics and psychotropic polypharmacy.