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Sarcosine in the management of schizophrenia

Published online by Cambridge University Press:  26 October 2020

Daniel Brennan*
Affiliation:
Retired Consultant Psychiatrist. Email: [email protected]
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Abstract

Type
Correspondence
Copyright
Copyright © The Royal College of Psychiatrists 2020

I read with interest the editorial in December 2019 on ‘A possible role for sarcosine in the management of schizophrenia’. Professor David Curtis did suggest that ‘it seems to be universally well tolerated with an absence of significant side-effects’.Reference Curtis1 I wonder if addition of sarcosine to medication for schizophrenia is actually safe for every patient. It is well accepted that sarcosine level increases in many cases of carcinoma of the prostate gland. Indeed, it may well be a marker for carcinoma of the prostate.Reference Kdadra, Höckner, Leung, Kremer and Schiffer2Reference Cernei, Heger, Gumulec, Zitka, Masarik and Babula4 It is thought that this elevated level of sarcosine is produced by the prostatic cancer cells. This does not mean that it causes the cancer. However, there are at least two important studies in the literature that comment on this issue. Sreekumar et alReference Sreekumar, Poisson, Rajendiran, Khan, Cao and Yu5 in Nature in 2009 found metabolomic profiles delineating a potential role for sarcosine in prostatic cancer progression and Khan et alReference Khan, Rajendiran, Ateeq, Asangani, Athanikar and Yocum6 in Neoplasia in 2013 found increased alteration of benign prostatic epithelial cells upon the addition of sarcosine to prostatic cells. I wondered therefore if a note of caution should be sounded about the use of sarcosine supplement in older men with schizophrenia, especially those with signs of prostatic hypertrophy. Prostate cancer is the most common cancer in males over 70 and the second most common cause of cancer deaths in men.

Declaration of interest

None.

References

Curtis, D. A possible role for sarcosine in the management of schizophrenia. Br J Psychiatry 2019; 215: 697–8.CrossRefGoogle ScholarPubMed
Kdadra, M, Höckner, S, Leung, H, Kremer, W, Schiffer, E. Metabolomics biomarkers of prostate cancer: a systematic review. Diagnostics (Basel) 2019; 9: 21.CrossRefGoogle ScholarPubMed
Koutros, S, Meyer, TE, Fox, SD, Issaq, HJ, Veenstra, TD, Huang, WY, et al. Prospective evaluation of serum sarcosine and risk of prostate cancer in the Prostate, Lung, Colorectal and Ovarian Cancer Screening Trial. Carcinogenesis 2013; 34: 2281–5.Google ScholarPubMed
Cernei, N, Heger, Z, Gumulec, J, Zitka, O, Masarik, M, Babula, P, et al. Sarcosine as a potential prostate cancer biomarker – a review. Int J Mol Sci 2013; 14: 13893–908.CrossRefGoogle ScholarPubMed
Sreekumar, A, Poisson, LM, Rajendiran, TM, Khan, AP, Cao, Q, Yu, J, et al. Metabolomic profiles delineate potential role for sarcosine in prostate cancer progression. Nature 2009; 457: 910–4.CrossRefGoogle ScholarPubMed
Khan, AP, Rajendiran, TM, Ateeq, B, Asangani, IA, Athanikar, JN, Yocum, AK, et al. The role of sarcosine metabolism in prostate cancer progression. Neoplasia 2013; 15: 491501.CrossRefGoogle ScholarPubMed
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