Maria Lidia Gerra
Research Subjects
Maria Lidia Gerra has a total of 23 co-authors. Here are the top co-authors by number of shared publications:
- Claudia Donnini
Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy
2 shared publications - Gilberto Gerra
Drug Prevention and Health Branch, Division for Operations, United Nations Office on Drugs and Crime, Vienna, Austria
2 shared publications - Lorenzo Somaini
Addiction Treatment Centre, Local Health Unit, Biella, Italy
2 shared publications - Paolo Ossola
University of Parma
2 shared publications A. Zaimovic
Servizio Tossicodipendenze, AUSL, Parma, Italy
1 shared publicationCarlo Marchesi
Department of Medicine and Surgery, University of Parma, Parma, Italy
1 shared publication
Latest Publications
- 1 December 2021
- Published by Elsevier in Neuroscience & Biobehavioral Reviews
- Vol. 131, 560-580
Early parent-child interactions and substance use disorder: An attachment perspective on a biopsychosocial entanglement
- 1 December 2021
- Published by Elsevier in Neuroscience & Biobehavioral Reviews
- Vol. 131, 560-580
Early parent-child interactions and substance use disorder: An attachment perspective on a biopsychosocial entanglement
- 19 November 2019
- Published by Springer Nature in International Journal of Behavioral Medicine
- Vol. 26 (6) , 673-679
Alexithymia and Cardiac Outcome in Patients at First Acute Coronary Syndrome
This cohort study was aimed to verify whether subjects at their first acute coronary syndrome (ACS) were more alexithymic than healthy controls (HC) and whether alexithymia can predispose patients with coronary artery disease to new major adverse cardiac events (MACE) during a 24-month follow-up period.
- 19 November 2019
- Published by Springer Nature in International Journal of Behavioral Medicine
- Vol. 26 (6) , 673-679
Alexithymia and Cardiac Outcome in Patients at First Acute Coronary Syndrome
This cohort study was aimed to verify whether subjects at their first acute coronary syndrome (ACS) were more alexithymic than healthy controls (HC) and whether alexithymia can predispose patients with coronary artery disease to new major adverse cardiac events (MACE) during a 24-month follow-up period.
- 1 May 2011
- Published by Bentham Science Publishers Ltd. in Recent Patents on CNS Drug Discovery
- Vol. 6 (2) , 146-160
Promising Medications for Cocaine Dependence Treatment
Cocaine dependence is characterized by compulsive drug seeking and high vulnerability to relapse. Overall, cocaine remains one of the most used illicit drugs in the world. Given the difficulty of achieving sustained recovery, pharmacotherapy of cocaine addiction remains one of the most important clinical challenges. Recent advances in neurobiology, brain imaging and clinical trials suggest that certain medications show promise in the treatment of cocaine addiction. The pharmacotherapeutic approaches for cocaine dependence include medications able to target specific subtypes of dopamine receptors, affect different neurotransmitter systems (i.e. noradrenergic, serotonergic, cholinergic, glutamatergic, GABAergic and opioidergic pathways), and modulate neurological processes. The systematic reviews concerning the pharmacological treatment of cocaine dependence appear to indicate controversial findings and inconclusive results. The aim of future studies should be to identify the effective medications matching the specific needs of patients with specific characteristics, abandoning the strategies extended to the entire population of cocaine dependent patients. In the present review we summarize the current pharmacotherapeutic approaches to the treatment of cocaine dependence with a focus on the new patents.
- 1 May 2011
- Published by Bentham Science Publishers Ltd. in Recent Patents on CNS Drug Discovery
- Vol. 6 (2) , 146-160
Promising Medications for Cocaine Dependence Treatment
Cocaine dependence is characterized by compulsive drug seeking and high vulnerability to relapse. Overall, cocaine remains one of the most used illicit drugs in the world. Given the difficulty of achieving sustained recovery, pharmacotherapy of cocaine addiction remains one of the most important clinical challenges. Recent advances in neurobiology, brain imaging and clinical trials suggest that certain medications show promise in the treatment of cocaine addiction. The pharmacotherapeutic approaches for cocaine dependence include medications able to target specific subtypes of dopamine receptors, affect different neurotransmitter systems (i.e. noradrenergic, serotonergic, cholinergic, glutamatergic, GABAergic and opioidergic pathways), and modulate neurological processes. The systematic reviews concerning the pharmacological treatment of cocaine dependence appear to indicate controversial findings and inconclusive results. The aim of future studies should be to identify the effective medications matching the specific needs of patients with specific characteristics, abandoning the strategies extended to the entire population of cocaine dependent patients. In the present review we summarize the current pharmacotherapeutic approaches to the treatment of cocaine dependence with a focus on the new patents.
- 12 October 2009
- Published by Wiley in American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
- Vol. 153B (3) , 715-722
Relevance of perceived childhood neglect, 5‐HTT gene variants and hypothalamus–pituitary–adrenal axis dysregulation to substance abuse susceptibility
The hypotheses of (1) gene × environment interaction in the susceptibility to experiment with drugs and (2) hypothalamus–pituitary–adrenal (HPA) axis involvement in mediating the effects of early adverse experiences and gene variants affecting serotonin function on substance abuse vulnerability were tested by investigating in 187 healthy adolescents the possible relevance of 5‐HTT “S” polymorphism, childhood parental neglect reported retrospectively and HPA axis function to the susceptibility to experiment with illicit drugs. Higher frequency of the 5‐HTT SS genotype seems to be associated with an increased susceptibility to use illegal psychotropic drugs among the adolescents. At the same time, reduced maternal care perception was found to represent a key intermediate factor of the association between SS polymorphism and drug use, suggesting that genetic factors and parental behavior concur to drug use susceptibility. Our results also confirm the relationship between basal plasma levels of cortisol and adrenocorticotropic hormone (ACTH) on the one hand, and retrospective measures of neglect during childhood: the higher the mother and father neglect CECA‐Q scores, the higher the plasma levels of the two HPA hormones. Such positive relationship has been proved to be particularly effective and important when associated to the S‐allele, both in homozygote and heterozygote individuals. However, when tested together with genotype and parental neglect, the effect of HPA hormones such as cortisol and ACTH was not found to improve significantly the explanatory power of the risk model.
- 12 October 2009
- Published by Wiley in American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
- Vol. 153B (3) , 715-722
Relevance of perceived childhood neglect, 5‐HTT gene variants and hypothalamus–pituitary–adrenal axis dysregulation to substance abuse susceptibility
The hypotheses of (1) gene × environment interaction in the susceptibility to experiment with drugs and (2) hypothalamus–pituitary–adrenal (HPA) axis involvement in mediating the effects of early adverse experiences and gene variants affecting serotonin function on substance abuse vulnerability were tested by investigating in 187 healthy adolescents the possible relevance of 5‐HTT “S” polymorphism, childhood parental neglect reported retrospectively and HPA axis function to the susceptibility to experiment with illicit drugs. Higher frequency of the 5‐HTT SS genotype seems to be associated with an increased susceptibility to use illegal psychotropic drugs among the adolescents. At the same time, reduced maternal care perception was found to represent a key intermediate factor of the association between SS polymorphism and drug use, suggesting that genetic factors and parental behavior concur to drug use susceptibility. Our results also confirm the relationship between basal plasma levels of cortisol and adrenocorticotropic hormone (ACTH) on the one hand, and retrospective measures of neglect during childhood: the higher the mother and father neglect CECA‐Q scores, the higher the plasma levels of the two HPA hormones. Such positive relationship has been proved to be particularly effective and important when associated to the S‐allele, both in homozygote and heterozygote individuals. However, when tested together with genotype and parental neglect, the effect of HPA hormones such as cortisol and ACTH was not found to improve significantly the explanatory power of the risk model.