Literature DB >> 24917847

The Correlation between Osteoporosis Occurrences in Both Schizophrenia and Parkinson's Disease.

Fatemeh Radaei1, Asma Darvishi2, Shahriar Gharibzadeh1.   

Abstract

Entities:  

Keywords:  AMPK; Parkinson’s disease; energy metabolism; osteoporosis; schizophrenia

Year:  2014        PMID: 24917847      PMCID: PMC4040489          DOI: 10.3389/fneur.2014.00083

Source DB:  PubMed          Journal:  Front Neurol        ISSN: 1664-2295            Impact factor:   4.003


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Osteoporosis disease is a metabolic disorder in which bone mineral density (BMD) is lower than the normal threshold. Based on literature, it is known that schizophrenic patients due to consuming anti-psychotic drugs and Parkinson’s disease patients due to vitamin D deficiency and decrease in mobility are at the high risk of osteoporosis (1–4). On the other hand, it is observed that adenosine 5′-monophosphate (AMP)-activated protein kinase (AMPK) activity, which is regulating cellular energy homeostasis, is reduced in schizophrenia diseases (5). In addition, it is known that there is mitochondrial dysfunction in Parkinson’s disease that can be treated by AMPK, which is identified as a mitochondrial biogenesis (6–8). Recently, some findings show that AMPK plays an important role in bone metabolism. Besides, some in vitro studies revealing that AMPK modulators regulate bone cell function (9–13). Also, some studies show that deficiency of AMPK α and β subunits in mice causes bone loss in vivo (14). Based on the above mentioned points, it can be referred that AMPK deficiency in Parkinson’s disease and schizophrenia may lead to osteoporosis. This can be used as a goal in treatment of osteoporosis in those disorders. In another word, nowadays there are some drugs available for both diseases but they have some side effect, which may lead to osteoporosis; by considering the fact that AMPK deficiency may cause osteoporosis, new drugs can be provided with AMPK supplement to reduce the osteoporosis symptoms. Surely, experimental trials are needed to validate our hypothesis.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
  14 in total

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Authors:  Richard I G Holt; Robert C Peveler
Journal:  Clin Endocrinol (Oxf)       Date:  2011-02       Impact factor: 3.478

Review 2.  Treatments for schizophrenia: a critical review of pharmacology and mechanisms of action of antipsychotic drugs.

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Journal:  Mol Psychiatry       Date:  2005-01       Impact factor: 15.992

Review 3.  Mitochondrial dysfunction in Parkinson's disease.

Authors:  Jianhui Zhu; Charleen T Chu
Journal:  J Alzheimers Dis       Date:  2010       Impact factor: 4.472

Review 4.  The role of AMP-activated protein kinase in mitochondrial biogenesis.

Authors:  Richard M Reznick; Gerald I Shulman
Journal:  J Physiol       Date:  2006-05-18       Impact factor: 5.182

5.  Germline deletion of AMP-activated protein kinase beta subunits reduces bone mass without altering osteoclast differentiation or function.

Authors:  Julian M W Quinn; Shanna Tam; Natalie A Sims; Hasnawati Saleh; Narelle E McGregor; Ingrid J Poulton; John W Scott; Matthew T Gillespie; Bruce E Kemp; B J W van Denderen
Journal:  FASEB J       Date:  2009-09-01       Impact factor: 5.191

Review 6.  Antipsychotics: impact on prolactin levels.

Authors:  Paul J Goodnick; Lucero Rodriguez; Orlando Santana
Journal:  Expert Opin Pharmacother       Date:  2002-10       Impact factor: 3.889

Review 7.  AMP-activated protein kinase pathway and bone metabolism.

Authors:  J Jeyabalan; M Shah; B Viollet; C Chenu
Journal:  J Endocrinol       Date:  2011-09-08       Impact factor: 4.286

8.  Abnormal levels of cAMP-dependent protein kinase regulatory subunits in platelets from schizophrenic patients.

Authors:  D Tardito; G B Tura; L Bocchio; S Bignotti; R Pioli; G Racagni; J Perez
Journal:  Neuropsychopharmacology       Date:  2000-08       Impact factor: 7.853

9.  Effect of metformin on bone marrow progenitor cell differentiation: in vivo and in vitro studies.

Authors:  M Silvina Molinuevo; Leon Schurman; Antonio D McCarthy; Ana M Cortizo; María J Tolosa; M Virginia Gangoiti; Veronica Arnol; Claudia Sedlinsky
Journal:  J Bone Miner Res       Date:  2010-02       Impact factor: 6.741

10.  Ghrelin is neuroprotective in Parkinson's disease: molecular mechanisms of metabolic neuroprotection.

Authors:  Jacqueline A Bayliss; Zane B Andrews
Journal:  Ther Adv Endocrinol Metab       Date:  2013-02       Impact factor: 3.565

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2.  Effects of Olanzapine on Bone Mineral Density, Glucose, and Lipid Metabolism in Schizophrenia Patients.

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