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1.
Int J Psychiatry Med ; 59(5): 521-535, 2024 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-38140979

RESUMEN

BACKGROUND: Comorbid major depressive disorder (MDD) and opium use disorder (OUD) are known to increase the risk of suicide. The purpose of this study was to compare the efficacy and safety of adjunctive therapy with either ketamine or buprenorphine in patients with comorbid MDD and OUD. METHODS: This was a randomized double-blind controlled trial in adults admitted to a hospital in Iran. Sixty-six participants were enrolled and received either ketamine or buprenorphine, along with current antidepressant therapy. The primary outcome was change in depressive symptoms assessed using the Beck Depression Inventory (BDI) after 2 hours, 24 hours, and 7 days following initiation of treatment. Secondary outcomes included changes in suicidal ideation, evaluated by the Beck Scale for Suicidal Ideation (BSSI). RESULTS: Both groups experienced a significant decrease in the severity of depression following the interventions (p < .05). However, there was no significant difference in the between-group comparison (p > .05). Both groups also exhibited a significant reduction in suicidal ideation compared to before the study, with the decrease in severity being over 85% in both groups (p < .05). CONCLUSION: Both ketamine and buprenorphine appear to be equally effective in reducing symptoms of depression and suicidal ideation among individuals with MDD and OUD.


Asunto(s)
Buprenorfina , Trastorno Depresivo Mayor , Ketamina , Ideación Suicida , Humanos , Trastorno Depresivo Mayor/tratamiento farmacológico , Trastorno Depresivo Mayor/epidemiología , Ketamina/uso terapéutico , Ketamina/administración & dosificación , Buprenorfina/uso terapéutico , Masculino , Adulto , Femenino , Método Doble Ciego , Quimioterapia Combinada , Antidepresivos/uso terapéutico , Irán , Persona de Mediana Edad , Comorbilidad , Adicción al Opio/tratamiento farmacológico , Adicción al Opio/epidemiología , Trastornos Relacionados con Opioides/tratamiento farmacológico , Adulto Joven
2.
Subst Use Misuse ; 53(10): 1726-1729, 2018 08 24.
Artículo en Inglés | MEDLINE | ID: mdl-29393724

RESUMEN

For several centuries, opium addiction has been a social problem all over the world. It has been prevalent in Iran from the Safavid era (1501-1736 A.D). During this period, Hakim Imad al-Din Mahmud ibn-Mas'ud Shirazi (1515-1592 A.D), also known as Imad was one of the Persian physicians who wrote one of the earliest books in the field of opium and addiction (called Afiounieh) in history. In this book, he introduced two sustained release rectal (suppository) and oral (pill) dosage forms for Muslim addicts who fast in the month of Ramadan. He aimed to formulate them for these people so that they could keep fasting by using the slow release drugs. In these formulations, his innovation has important impacts in the history of both addiction and pharmaceutical sciences.


Asunto(s)
Preparaciones de Acción Retardada/uso terapéutico , Adicción al Opio/tratamiento farmacológico , Religión y Medicina , Administración Oral , Libros , Preparaciones de Acción Retardada/administración & dosificación , Preparaciones de Acción Retardada/historia , Historia del Siglo XVI , Historia del Siglo XVII , Historia del Siglo XVIII , Humanos , Islamismo , Persia , Médicos , Supositorios , Terapias en Investigación/historia
3.
J Psychoactive Drugs ; 49(3): 242-251, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28632076

RESUMEN

Genetic association of rs678849 along with neuroimaging and biomarker phenotypes, parallel with the known involvements of the OPRD1 in drug abuse, provided additional support for targeting these receptors as potential therapeutic targets in both neurodegenerative diseases and neuropsychiactric disorders such as Alzheimer's disease. Samples were selected among 202 opium-addicted participants undergoing methadone treatment and 202 healthy controls. Genomic DNA of all subjects was extracted from whole blood samples through a Salting Out procedure. Four variants (rs678849, 2236857, 2236855, and 760589) were genotyped in the studied subjects using ARMS-PCR. The analysis was performed using SNPalyze and SPSS ver.20 software. According to single locus analysis, rs678849 under dominant model (p < 0.001), rs2236857 under recessive model (p = 0.006), and the two variants, rs2236855 and rs760589 under co-dominant model, showed significant contributions between groups (p = 0.001 and p = 0.009, respectively). rs2236855 was associated with the development of libido dysfunction in opium-addicted patients undergoing methadone treatment (p = 0.011). Through haplotype analyses, five haplotypes with frequency of more than 5% displayed significant association with opioid dependence in study participants. In conclusion, the four studied OPRD1 gene variants and their haplotypes can play important roles in susceptibility to opioid dependence.


Asunto(s)
Metadona/uso terapéutico , Narcóticos/uso terapéutico , Tratamiento de Sustitución de Opiáceos/métodos , Adicción al Opio/genética , Receptores Opioides delta/genética , Adulto , Humanos , Irán , Libido/efectos de los fármacos , Masculino , Adicción al Opio/tratamiento farmacológico
4.
Drug Alcohol Depend ; 176: 117-125, 2017 07 01.
Artículo en Inglés | MEDLINE | ID: mdl-28531768

RESUMEN

BACKGROUND: Some patients with opioid use disorder (OUD) are treated with methadone maintenance therapy (MMT). However, as with opioids, methadone has major side-effects; sexual dysfunction is a particularly distressing such effect. Rosa Damascena oil has been shown to reduce subjective sexual dysfunction in patients with major depressive disorders, but its influence on testosterone has not so far been tested. The aim of the present study was to investigate the influence of Rosa Damascena oil on sexual dysfunction and testosterone levels among male patients with OUD and undergoing MMT. METHODS: A total of 50 male patients (mean age: 40 years) diagnosed with OUD and receiving MMT were randomly assigned either to the Rosa Damascena oil (drops) or a placebo condition. At baseline, and four and eight weeks later, patients completed questionnaires covering sexual and erectile function. Blood samples to assess testosterone levels were taken at baseline and eight weeks later on completion of the study. RESULTS: Over time sexual dysfunction decreased, and testosterone increased in the Rosa Damascena oil, but not in the placebo condition. Sexual dysfunction scores and testosterone levels were not consistently related. CONCLUSIONS: Results from this double-blind, randomized, and placebo-controlled clinical trial showed that Rosa Damascena oil improved sexual function and testosterone levels among males with OUD and undergoing MMT.


Asunto(s)
Metadona/efectos adversos , Tratamiento de Sustitución de Opiáceos/efectos adversos , Fitoterapia/métodos , Aceites de Plantas/uso terapéutico , Rosa/química , Disfunciones Sexuales Psicológicas/tratamiento farmacológico , Adulto , Método Doble Ciego , Humanos , Masculino , Adicción al Opio/tratamiento farmacológico , Conducta Sexual/efectos de los fármacos , Disfunciones Sexuales Psicológicas/sangre , Disfunciones Sexuales Psicológicas/inducido químicamente , Testosterona/sangre
5.
Psychopharmacol Bull ; 47(1): 48-51, 2017 01 26.
Artículo en Inglés | MEDLINE | ID: mdl-28138205

RESUMEN

Two patients with opium dependence developed delirium during abstinence. The delirium resolved completely within 48-58 hours of appropriate treatment. Caution needs to be exercised during opioid detoxification in timely detecting and treating potentially life-threatening condition like delirium.


Asunto(s)
Delirio/etiología , Trastornos Relacionados con Opioides/complicaciones , Opio/efectos adversos , Síndrome de Abstinencia a Sustancias/complicaciones , Adulto , Analgésicos Opioides/uso terapéutico , Anticonvulsivantes/uso terapéutico , Clonazepam/uso terapéutico , Humanos , Masculino , Persona de Mediana Edad , Adicción al Opio/tratamiento farmacológico , Síndrome de Abstinencia a Sustancias/tratamiento farmacológico , Síndrome de Abstinencia a Sustancias/etiología , Tramadol/uso terapéutico
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