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Relationship between antipsychotic medication, serum prolactin levels and osteoporosis/osteoporotic fractures in patients with schizophrenia: a critical literature review.

AbstractINTRODUCTION:
Using an antipsychotic medication can increase prolactin (PRL) levels, causing hyperprolactinemia (HPRL). Although the occurrence of osteoporosis within the population of patients with schizophrenia has been recognized, the precise nature of the association between antipsychotic treatment, PRL, osteoporosis, and the disease itself seems to be elusive.
AREAS COVERED:
The aim of this review is to critically review the literature regarding the association between osteoporosis and PRL and to summarize the available evidence with respect to the impact of PRL-elevating antipsychotics on bone mineral density (BMD) and fractures in non-elderly patients with schizophrenia.
EXPERT OPINION:
Although long-standing HPRL can have an impact on the rate of bone metabolism and, when associated with hypogonadism, may lead to decreased bone density in both female and male subjects, the relative contribution of antipsychotic-induced HPRL in bone mineral loss in patients with schizophrenia remains unclear. Methodological shortcomings of existing studies, including the lack of prospective data and the focus on measurements of BMD instead of bone turnover markers, preclude definitive conclusions regarding the relationship between PRL-raising antipsychotics and BMD loss in patients with schizophrenia. Therefore, more well conducted prospective trials of these biomarkers are necessary to establish the precise relationship between antipsychotics, PRL levels and osteoporosis/osteoporotic risk.
AuthorsMarc De Hert, Johan Detraux, Brendon Stubbs
JournalExpert opinion on drug safety (Expert Opin Drug Saf) Vol. 15 Issue 6 Pg. 809-23 (Jun 2016) ISSN: 1744-764X [Electronic] England
PMID26986209 (Publication Type: Journal Article, Review)
Chemical References
  • Antipsychotic Agents
  • Prolactin
Topics
  • Antipsychotic Agents (adverse effects, therapeutic use)
  • Bone Density (drug effects)
  • Female
  • Humans
  • Hyperprolactinemia (chemically induced, complications)
  • Male
  • Osteoporosis (epidemiology, etiology)
  • Osteoporotic Fractures (epidemiology, etiology)
  • Prolactin (blood)
  • Schizophrenia (complications, drug therapy)

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