Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 May 14;33(3):e100192.
doi: 10.1136/gpsych-2020-100192. eCollection 2020.

Association of the HTR2C-759C/T polymorphism and antipsychotic-induced weight gain: a meta-analysis

Affiliations

Association of the HTR2C-759C/T polymorphism and antipsychotic-induced weight gain: a meta-analysis

Yan Chen et al. Gen Psychiatr. .

Abstract

Background: Antipsychotic-induced weight gain (AIWG) is a crucial factor for the medication cessation of patients with schizophrenia. Multiple studies have shown that the functional polymorphism -759 C/T (rs3813929) in the HTR2C promoter region could possibly be correlated with AIWG.

Aim: To evaluate the genetic association of the HTR2C-759C/T polymorphism and AIWG in patients with schizophrenia with antipsychotic drugs (APDs) administration.

Methods: Eligible studies were identified by searching the following databases: PubMed, Embase, Web of Science, China Nation Knowledge Infrastructure (CNKI), VIP, Wanfang Data, Chinese Biomedical Literature Database (CBM) and the Airiti Library. The quality of studies was evaluated based on the Newcastle-Ottawa Scale. The pooled OR and 95% CI were calculated for the dominant (CT/TT/T vs CC/C) mode, and subgroup analyses were performed based on ethnicity, antipsychotic medication and gender; all statistical analyses were performed using the statistical software STATA V.12.0.

Result: A total of 17 studies with 3170 patients with schizophrenia were included in our meta-analysis. The result of the meta-analysis has shown that the association between the -759 C/T polymorphism and AIWG is statistically significant (OR 0.34, 95% CI: 0.20 to 0.57, z=4.11, p<0.001). The subgroup analyses revealed significant correlations between the -759 C/T polymorphism and AIWG in the Caucasian population (OR 0.33, 95% CI: 0.14 to 0.77, z=2.55, p=0.011), the Asian population (OR 0.31, 95% CI: 0.18 to 0.52, z=4.46, p<0.001), the patients with APDs administration (CT/TT/T vs CC/C: OR 0.63, 95% CI: 0.40 to 1.00, z=1.97, p=0.049) and the patients with atypical antipsychotic drug administration (CT/TT/T vs CC/C: OR 0.21, 95% CI: 0.09 to 0.47, z=3.83, p<0.001). The sensitivity analysis showed that the results were stable. Begg's test (after correction z=1.07, p=0.287) and Egger's test (t=-2.41, p=0.029) show that the included articles have no significant publication bias.

Conclusion: There is a significant genetic association between HTR2C-759C/T and AIWG, and patients with T allele are less likely to have AIWG.

Keywords: meta-analysis as topic; schizophrenia.

PubMed Disclaimer

Conflict of interest statement

Competing interests: None declared.

Figures

Figure 1
Figure 1
Flowchart of the search process
Figure 2
Figure 2
Meta-analysis forest plot of the genetic correlation of HTR2C-759C/T polymorphism and antipsychotic-induced weight gain (subgroup analysis based on ethnicity).
Figure 3
Figure 3
Meta-analysis forest plot of the genetic association between HTR2C-759C/T polymorphism and antipsychotic-induced weight gain (subgroup analysis based on the type of antipsychotic medication). AAP, atypical antipsychotic drug; APD, antipsychotic drug.
Figure 4
Figure 4
Sensitivity analysis.
Figure 5
Figure 5
Begg’s funnel plot.

References

    1. Lieberman JA. Effectiveness of antipsychotic drugs in patients with chronic schizophrenia: efficacy, safety and cost outcomes of CATIE and other trials. J Clin Psychiatry 2007;68:e04. 10.4088/jcp.0207e04 - DOI - PubMed
    1. Raben AT, Marshe VS, Chintoh A, et al. The complex relationship between antipsychotic-induced weight gain and therapeutic benefits: a systematic review and implications for treatment. Front Neurosci 2017;11:741. 10.3389/fnins.2017.00741 - DOI - PMC - PubMed
    1. Jeon SW, Kim Y-K. Unresolved issues for utilization of atypical antipsychotics in schizophrenia: antipsychotic polypharmacy and metabolic syndrome. Int J Mol Sci 2017;18:2174. 10.3390/ijms18102174 - DOI - PMC - PubMed
    1. Puangpetch A, Unaharassamee W, Jiratjintana N, et al. Genetic polymorphisms of HTR2C, Lep and Lepr on metabolic syndromes in patients treated with atypical antipsychotic drugs. J Pharm Pharmacol 2018;70:536–42. 10.1111/jphp.12892 - DOI - PubMed
    1. Blundell JE. Is there a role for serotonin (5-hydroxytryptamine) in feeding? Int J Obes 1977;1:15–42. - PubMed

LinkOut - more resources