José A. Monreal

Prof. José A. Monreal

Hospital Mútua de Terrassa, Terrassa
orcid

Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2006 in Psychoneuroendocrinology
Verified
Journal Article
Closed access
FDFabrice Duval
Fabrice Duval
MMMarie-Claude Mokrani
Marie-Claude Mokrani
José A. MonrealJosé A. Monreal
José A. Monreal
SFSaïd Fattah
Saïd Fattah
CCChristiane Champeval
Christiane Champeval
JMJean-Paul Macher
Jean-Paul Macher


28 February 2017 in Brain Imaging and Behavior
Verified
Journal Article
Closed access
PDF file
DVDaniel Vega
Daniel Vega
PRPablo Ripollés
Pablo Ripollés
ÀSÀngel Soto
Àngel Soto
RTRafael Torrubia
Rafael Torrubia
JRJoan Ribas
Joan Ribas
JMJosep Marco-Pallarés
Josep Marco-Pallarés

Alexandre Gonzalez-RodriguezAlexandre Gonzalez-Rodriguez
Alexandre Gonzalez-Rodriguez
AGArmand Guàrdia
Armand Guàrdia
APAida Álvarez Pedrero
Aida Álvarez Pedrero
MBMaria Betriu
Maria Betriu
Jesus CoboJesus Cobo
Jesus Cobo
Javier LabadJavier Labad
Javier Labad
Women with schizophrenia show sex-specific health needs that differ according to stage of life. The aim of this narrative review is to resolve important questions concerning the treatment of women with schizophrenia at different periods of their life—paying special attention to reproductive and post-reproductive stages. Review results suggest that menstrual cycle-dependent treatments may be a useful option for many women and that recommendations re contraceptive options need always to be part of care provision. The pregnancy and the postpartum periods—while constituting vulnerable time periods for the mother—require special attention to antipsychotic effects on the fetus and neonate. Menopause and aging are further vulnerable times, with extra challenges posed by associated health risks. Pregnancy complications, neurodevelopmental difficulties of offspring, cancer risk and cognitive defects are indirect results of the interplay of hormones and antipsychotic treatment of women over the course of the lifespan. The literature recommends that health promotion strategies need to be directed at lifestyle modifications, prevention of medical comorbidities and increased psychosocial support. Careful monitoring of pharmacological treatment has been shown to be critical during periods of hormonal transition. Not only does treatment of women with schizophrenia often need to be different than that of their male peers, but it also needs to vary over the course of life.

1 November 2004 in Psychoneuroendocrinology
Verified
Journal Article
Closed access
FDFabrice Duval
Fabrice Duval
MCMarc-Antoine Crocq
Marc-Antoine Crocq
MGMarie-Sabine Guillon
Marie-Sabine Guillon
MMMarie-Claude Mokrani
Marie-Claude Mokrani
José A. MonrealJosé A. Monreal
José A. Monreal
JMJean-Paul Macher
Jean-Paul Macher

Javier LabadJavier Labad
Javier Labad
NSNeus Salvat-Pujol
Neus Salvat-Pujol
AAAntonio Armario
Antonio Armario
ÁCÁngel Cabezas
Ángel Cabezas
AAAida de Arriba-Arnau
Aida de Arriba-Arnau
VSVirginia Soria
Virginia Soria
Sleep plays a crucial role in cognitive processes. Sleep and wake memory consolidation seem to be regulated by glucocorticoids, pointing out the potential role of the hypothalamic-pituitary-adrenal (HPA) axis in the relationship between sleep quality and cognitive abilities. Trait anxiety is another factor that is likely to moderate the relationship between sleep and cognition, because poorer sleep quality and subtle HPA axis abnormalities have been reported in people with high trait anxiety. The current study aimed to explore whether HPA axis activity or trait anxiety moderate the relationship between sleep quality and cognitive abilities in healthy individuals. We studied 203 healthy individuals. We measured verbal and visual memory, working memory, processing speed, attention and executive function. Sleep quality was assessed with the Pittsburgh Sleep Quality Index. Trait anxiety was assessed with the State-Trait Anxiety Inventory. HPA axis measures included the cortisol awakening response (CAR), diurnal cortisol slope and cortisol levels during the day. Multiple linear regression analyses explored the relationship between sleep quality and cognition and tested potential moderating effects by HPA axis measures and trait anxiety. Poor sleep quality was associated with poorer performance in memory, processing speed and executive function tasks. In people with poorer sleep quality, a blunted CAR was associated with poorer verbal and visual memory and executive functions, and higher cortisol levels during the day were associated with poorer processing speed. Trait anxiety was a moderator of visual memory and executive functioning. These results suggest that subtle abnormalities in the HPA axis and higher trait anxiety contribute to the relationship between lower sleep quality and poorer cognitive functioning in healthy individuals.