Association between common variants near the melanocortin 4 receptor gene and severe antipsychotic drug-induced weight gain

Abstract

Context: Second-generation antipsychotics (SGAs) are increasingly used in the treatment of many psychotic and nonpsychotic disorders. Unfortunately, SGAs are often associated with substantial weight gain, with no means to predict which patients are at greatest risk.

Objective: To identify single-nucleotide polymorphisms associated with antipsychotic drug–induced weight gain.

Design: Pharmacogenetic association study.

Setting: The discovery cohort was from a US general psychiatric hospital. Three additional cohorts were from psychiatric hospitals in the United States and Germany and from a European antipsychotic drug trial.

Participants: The discovery cohort consisted of 139 pediatric patients undergoing first exposure to SGAs. The 3 additional cohorts consisted of 73, 40, and 92 subjects.

Intervention: Patients in the discovery cohort were treated with SGAs for 12 weeks. Additional cohorts were treated for 6 and 12 weeks.

Main outcome measures: We conducted a genomewide association study assessing weight gain associated with 12 weeks of SGA treatment in patients undergoing first exposure to antipsychotic drugs. We next genotyped 3 independent cohorts of subjects assessed for antipsychotic drug-induced weight gain.

Results: Our genome-wide association study yielded 20 single-nucleotide polymorphisms at a single locus exceeding a statistical threshold of P<10(-5). This locus, near the melanocortin 4 receptor (MC4R) gene, overlaps a region previously identified by large-scale genome-wide association studies of obesity in the general population. Effects were recessive, with minor allele homozygotes gaining extreme amounts of weight during the 12-week trial. These results were replicated in 3 additional cohorts, with rs489693 demonstrating consistent recessive effects; meta-analysis revealed a genome-wide significant effect (P=5.59 X 10 (-12). Moreover, we observed consistent effects on related metabolic indices, including triglyceride, leptin, and insulin levels.

Conclusions: These data implicate MC4R in extreme SGA-induced weight gain and related metabolic disturbances. A priori identification of high-risk subjects could lead to alternative treatment strategies in this population.

Figures

Figure 1

Distribution of antipsychotic-drug induced weight gain in antipsychotic naïve subjects following 12 weeks of treatment with second-generation antipsychotic drugs. QTP = quetiapine; RIS = risperidone; ARI = aripiprazole; AVG = average of QTP, RIS and ARI; OLZ = olanzapine. The Y-axis represents the percentage of subjects in each of five weight gain categories:e.g.,subjects gaining > 21% of their baseline weight (red); subjects gaining >14% of their baseline weight (orange), etc.

Figure 2. Genome-wide Association Study Results

a. Manhattan plot displaying statistical significance levels (−log10P-values) of correlation/trend tests for change in BMI in the discovery cohort, plotted by chromosomal position for all autosomal SNPs. Peak values are observed on chromosome 18, between positions 55.934MB and 56.037MB, as detailed in Table 1A. b. Q–Q plot displaying statistical significance levels (−log10P-values) of correlation/trend tests for change in BMI in the discovery cohort, plotted against expected values under the null hypothesis. With the exception of the most strongly associated SNPs on chromosome 18, there is no deviation from the diagonal (λGC=1.00).

Figure 3

rs489693 genotype and antipsychotic-induced weight gain in four cohorts of subjects.