Antipsychotics and the risk of diabetes and death among adults with serious mental illnesses

• Published in: Psychological medicine 2023-12, Vol.53 (16), p.7677-7684
• Main Authors: Poulos, Jason, Normand, Sharon-Lise T., Zelevinsky, Katya, Newcomer, John W., Agniel, Denis, Abing, Haley K., Horvitz-Lennon, Marcela
• Format: Article
• Language: English
• Subjects: Antidiabetics; Antipsychotics; Aripiprazole; Cardiovascular disease; Death & dying; Diabetes; Diabetes mellitus; Diagnosis; Drugs; Enrollments; Ethnicity; Haloperidol; Medicaid; Medical diagnosis; Medicare; Mental disorders; Metabolism; Minority & ethnic groups; Morbidity; Mortality; Observational studies; Olanzapine; Older people; Original; Original Article; Psychotropic drugs; Quetiapine; Race; Risk assessment; Risk factors; Risk reduction; Risperidone; Schizophrenia; Second generation; Sensitivity analysis; Ziprasidone
• ISSN: 0033-2917; 1469-8978; 1469-8978
• DOI: 10.1017/S0033291723001502

Individuals with schizophrenia exposed to second-generation antipsychotics (SGA) have an increased risk for diabetes, with aripiprazole purportedly a safer drug. Less is known about the drugs' mortality risk or whether serious mental illness (SMI) diagnosis or race/ethnicity modify these effects. Authors created a retrospective cohort of non-elderly adults with SMI initiating monotherapy with an SGA (olanzapine, quetiapine, risperidone, and ziprasidone, aripiprazole) or haloperidol during 2008-2013. Three-year diabetes incidence or all-cause death risk differences were estimated between each drug and aripiprazole, the comparator, as well as effects within SMI diagnosis and race/ethnicity. Sensitivity analyses evaluated potential confounding by indication. 38 762 adults, 65% White and 55% with schizophrenia, initiated monotherapy, with haloperidol least (6%) and quetiapine most (26·5%) frequent. Three-year mortality was 5% and diabetes incidence 9.3%. Compared with aripiprazole, haloperidol and olanzapine reduced diabetes risk by 1.9 (95% CI 1.2-2.6) percentage points, or a 18.6 percentage point reduction relative to aripiprazole users' unadjusted risk (10.2%), with risperidone having a smaller advantage. Relative to aripiprazole users' unadjusted risk (3.4%), all antipsychotics increased mortality risk by 1.1-2.2 percentage points, representing 32.4-64.7 percentage point increases. Findings within diagnosis and race/ethnicity were generally consistent with overall findings. Only quetiapine's higher mortality risk held in sensitivity analyses. Haloperidol's, olanzapine's, and risperidone's lower diabetes risks relative to aripiprazole were not robust in sensitivity analyses but quetiapine's higher mortality risk proved robust. Findings expand the evidence on antipsychotics' risks, suggesting a need for caution in the use of quetiapine among individuals with SMI.