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Published Online: 1 April 2014

Lower Risk for Body Weight Gain and Better Control of Appetite After Switching Risperidone to Paliperidone in a Schizoaffective Patient

Publication: The Journal of Neuropsychiatry and Clinical Neurosciences
To the Editor: Paliperidone, a metabolite of risperidone, can also treat schizoaffective disorder. Its characteristics in metabolic profile remain controversial in recent years.1,2 However, I want to present a schizoaffective patient with a lower risk for body weight gain and a better control of appetite after switching from risperidone to paliperidone.

Case Report

Miss C, a 43-year-old woman with schizoaffective disorder, received risperidone 5 mg/day and duloxetine 60 mg/day for 2 to 3 years. She had significant improvements of psychotic symptoms and depression symptoms [Brief Psychiatric Rating Scale-18 (BPRS-18) scores: 13 and Hamilton Rating Scales for Depression-17 (HDRS-17) scores: 8]. She also had a stable job in the environmental protection agency of the government. However, she had progressive body weight gain problems associated with increased appetite since the use of risperidone and duloxetine [body mass index (BMI): 29.58‒31.79; body weight: 84‒99 kg within 2 years]. She started to worry a lot about persistent body weight gain and related metabolic syndrome. After careful consideration about the balance between the worsening of psychotic symptoms and persistent body weight gain problems, the risperidone 5 mg/day was switched to paliperidone 9 mg/day. We still continued duloxetine 60 mg/day in her treatment regimen. After a 2-month paliperidone treatment, her psychotic symptoms remained stable (BPRS-18 score: 12 and HDRS-17 score: 7), and her appetite started to decline with a decrease in body weight (BMI scores 30.75; body weight: 91.5 kg). No significant side effects after the switch of the antipsychotics were observed. She felt more satisfied with the improvement in quality of life, clear thinking, and less inattention after switching to paliperidone.

Discussion

In this case, risperidone is related to significant body weight gain and increased appetite. The switch to paliperidone can lead to less body weight gain without significant exacerbation of psychotic symptoms. Nasrallah et al. suggested that the dopamine D2 receptor and serotonin receptor affinity might be related to body weight side effects of risperidone.3 The review of oral paliperidone showed that paliperidone might decrease cholesterol and low density lipoprotein.1 However, Nussbaum and Stroup found that paliperidone might cause body weight gain.2 In a head-to-head study, paliperidone showed superiority over olanzapine in the metabolic side effect profile, insulin resistance, elevated triglyceride, and weight gain.4 Meltzer et al. reported that paliperidone even can show no significant differences of in weight gain, glucose handling, and lipid metabolism compared with the placebo group.5 In a 30-week trial, paliperidone showed no significant weight gain and relatively safe profile.6 However, the results of several studies were against the lower weight gain result of paliperidone.79 Kim et al. suggested that paliperidone-related weight gain might only occur in one out of four patients who received paliperidone treatment.10 Kim et al.’s study might provide an optimal solution for paliperidone-related weight gain. This case might belong to another group with no significant weight gain under paliperidone treatment. The switch management might provide us with a treatment choice when facing risperidone-related significant weight gain and fear of exacerbations of psychotic symptoms while switch to another kind of atypical antipsychotic.

References

1.
Yang LP: Oral paliperidone: a review of its use in the management of schizoaffective disorder. CNS Drugs 2011; 25:523–538
2.
Nussbaum A, Stroup TS: Paliperidone for schizophrenia. Cochrane Database Syst Rev 2008;2:CD006369
3.
Nasrallah HA: Atypical antipsychotic-induced metabolic side effects: insights from receptor-binding profiles. Mol Psychiatry 2008; 13:27–35
4.
Schreiner A, Niehaus D, Shuriquie NA, et al.: Metabolic effects of paliperidone extended release versus oral olanzapine in patients with schizophrenia: a prospective, randomized, controlled trial. J Clin Psychopharmacol 2012; 32:449–457
5.
Meltzer HY, Bobo WV, Nuamah IF, et al.: Efficacy and tolerability of oral paliperidone extended-release tablets in the treatment of acute schizophrenia: pooled data from three 6-week, placebo-controlled studies. J Clin Psychiatry 2008; 69:817–829
6.
Tzimos A, Samokhvalov V, Kramer M, et al.: Safety and tolerability of oral paliperidone extended-release tablets in elderly patients with schizophrenia: a double-blind, placebo-controlled study with six-month open-label extension. Am J Geriatr Psychiatry 2008; 16:31–43
7.
De Hert M, Yu W, Detraux J, et al.: Body weight and metabolic adverse effects of asenapine, iloperidone, lurasidone and paliperidone in the treatment of schizophrenia and bipolar disorder: a systematic review and exploratory meta-analysis. CNS Drugs 2012; 26:733–759
8.
Hu S, Yao M, Peterson BS, et al. A randomized, 12-week study of the effects of extended-release paliperidone (paliperidone ER) and olanzapine on metabolic profile, weight, insulin resistance, and beta-cell function in schizophrenic patients. Psychopharmacology (Berl) 2013;
9.
Turkoz I, Bossie CA, Lindenmayer JP, et al.: Paliperidone ER and oral risperidone in patients with schizophrenia: a comparative database analysis. BMC Psychiatry 2011; 11:21
10.
Kim SW, Yoon JS, Kim YS, et al.: The effect of paliperidone extended release on subjective well-being and responses in patients with schizophrenia. Prog Neuropsychopharmacol Biol Psychiatry 2012; 38:228–235

Information & Authors

Information

Published In

Go to The Journal of Neuropsychiatry and Clinical Neurosciences
Go to The Journal of Neuropsychiatry and Clinical Neurosciences
The Journal of Neuropsychiatry and Clinical Neurosciences
Pages: E36 - E37
PubMed: 24763786

History

Published online: 1 April 2014
Published in print: Spring 2014

Authors

Details

Yi-Cheng Hou, M.Sc.
Department of Nutrition, Buddhist Tzu-Chi General Hospital, Taipei Branch, New Taipei City, Taiwan
Chien-Han Lai, M.D.
Department of Psychiatry, Cheng Hsin General Hospital, Taipei City, Taiwan, ROC

Notes

Send correspondence to Dr. Lai; email: [email protected]

Competing Interests

The authors report no financial relationship with commercial interests.

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