questionsmedicales.fr
Acides aminés, peptides et protéines
Protéines
Hémoprotéines
Cytochromes
Cytochrome P-450 enzyme system
Famille-1 de cytochromes P450
Cytochrome P-450 CYP1A2
Cytochrome P-450 CYP1A2 : Questions médicales fréquentes
Termes MeSH sélectionnés :
Tissue Plasminogen Activator
Diagnostic
5
Cytochrome P-450
Métabolisme des médicaments
Tests sanguins
Cytochrome P-450
Biomarqueurs
Cytochrome P-450
Médicaments
Cytochrome P-450
Tests génétiques
Polymorphisme génétique
Symptômes
5
Dysfonction hépatique
Effets indésirables
Toxicité médicamenteuse
Cytochrome P-450
Induction enzymatique
Efficacité médicamenteuse
Réactions indésirables
Troubles hépatiques
Maladies
Métabolisme des médicaments
Prévention
5
Interactions médicamenteuses
Cytochrome P-450
Éducation médicale
Surveillance médicale
Alimentation
Cytochrome P-450
Toxicité médicamenteuse
Cytochrome P-450
Traitements
5
Ajustement médicamenteux
Cytochrome P-450
Médicaments
Antidépresseurs
Induction enzymatique
Ajustement médicamenteux
Effets indésirables
Surveillance médicale
Traitements alternatifs
Cytochrome P-450
Complications
5
Complications médicales
Réactions indésirables
Maladies hépatiques
Cytochrome P-450
Gestion des complications
Surveillance médicale
Surdosage
Cytochrome P-450
Santé chronique
Dysfonction hépatique
Facteurs de risque
5
Facteurs de risque
Génétique
Tabagisme
Induction enzymatique
Alcool
Inhibition enzymatique
Antibiotiques
Antidépresseurs
Alimentation
Cytochrome P-450
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"name": "Comment évaluer l'activité de CYP1A2 ?",
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{
"@type": "Question",
"name": "Quels tests sanguins sont utilisés pour CYP1A2 ?",
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{
"@type": "Question",
"name": "Quels sont les tests génétiques pour CYP1A2 ?",
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{
"@type": "Question",
"name": "Quels symptômes indiquent une dysfonction de CYP1A2 ?",
"position": 6,
"acceptedAnswer": {
"@type": "Answer",
"text": "Une dysfonction peut entraîner des effets indésirables liés à l'accumulation de médicaments."
}
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{
"@type": "Question",
"name": "Comment CYP1A2 affecte-t-il les symptômes de toxicité ?",
"position": 7,
"acceptedAnswer": {
"@type": "Answer",
"text": "Une activité réduite de CYP1A2 peut augmenter la toxicité des médicaments métabolisés."
}
},
{
"@type": "Question",
"name": "Y a-t-il des symptômes liés à l'induction de CYP1A2 ?",
"position": 8,
"acceptedAnswer": {
"@type": "Answer",
"text": "L'induction peut réduire l'efficacité des médicaments, entraînant des symptômes de maladie."
}
},
{
"@type": "Question",
"name": "Quels signes cliniques sont associés à CYP1A2 ?",
"position": 9,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les signes peuvent inclure des réactions indésirables aux médicaments et des troubles hépatiques."
}
},
{
"@type": "Question",
"name": "CYP1A2 influence-t-il les symptômes de maladies ?",
"position": 10,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, CYP1A2 peut influencer les symptômes de maladies en modifiant le métabolisme des médicaments."
}
},
{
"@type": "Question",
"name": "Comment prévenir les interactions médicamenteuses avec CYP1A2 ?",
"position": 11,
"acceptedAnswer": {
"@type": "Answer",
"text": "Évitez les médicaments connus pour interagir avec CYP1A2 et consultez un médecin."
}
},
{
"@type": "Question",
"name": "Y a-t-il des mesures préventives pour CYP1A2 ?",
"position": 12,
"acceptedAnswer": {
"@type": "Answer",
"text": "Des mesures incluent l'éducation sur les médicaments et la surveillance des effets."
}
},
{
"@type": "Question",
"name": "Comment le mode de vie influence-t-il CYP1A2 ?",
"position": 13,
"acceptedAnswer": {
"@type": "Answer",
"text": "Un mode de vie sain, y compris l'alimentation, peut influencer l'activité de CYP1A2."
}
},
{
"@type": "Question",
"name": "Quels aliments affectent CYP1A2 ?",
"position": 14,
"acceptedAnswer": {
"@type": "Answer",
"text": "Des aliments comme le brocoli et le pamplemousse peuvent influencer l'activité de CYP1A2."
}
},
{
"@type": "Question",
"name": "Comment éviter la toxicité liée à CYP1A2 ?",
"position": 15,
"acceptedAnswer": {
"@type": "Answer",
"text": "Évitez les doses élevées de médicaments métabolisés par CYP1A2 pour prévenir la toxicité."
}
},
{
"@type": "Question",
"name": "Comment traiter une dysfonction de CYP1A2 ?",
"position": 16,
"acceptedAnswer": {
"@type": "Answer",
"text": "Le traitement implique l'ajustement des doses de médicaments métabolisés par CYP1A2."
}
},
{
"@type": "Question",
"name": "Quels médicaments affectent CYP1A2 ?",
"position": 17,
"acceptedAnswer": {
"@type": "Answer",
"text": "Des médicaments comme la caféine et certains antidépresseurs peuvent influencer CYP1A2."
}
},
{
"@type": "Question",
"name": "Y a-t-il des traitements pour l'induction de CYP1A2 ?",
"position": 18,
"acceptedAnswer": {
"@type": "Answer",
"text": "L'induction peut nécessiter des ajustements de traitement pour éviter l'inefficacité."
}
},
{
"@type": "Question",
"name": "Comment gérer les effets indésirables liés à CYP1A2 ?",
"position": 19,
"acceptedAnswer": {
"@type": "Answer",
"text": "La gestion implique la surveillance des effets indésirables et l'ajustement des doses."
}
},
{
"@type": "Question",
"name": "Quels sont les traitements alternatifs pour CYP1A2 ?",
"position": 20,
"acceptedAnswer": {
"@type": "Answer",
"text": "Des traitements alternatifs peuvent inclure des médicaments non métabolisés par CYP1A2."
}
},
{
"@type": "Question",
"name": "Quelles complications peuvent survenir avec CYP1A2 ?",
"position": 21,
"acceptedAnswer": {
"@type": "Answer",
"text": "Des complications incluent des réactions indésirables graves aux médicaments métabolisés."
}
},
{
"@type": "Question",
"name": "CYP1A2 peut-il causer des maladies hépatiques ?",
"position": 22,
"acceptedAnswer": {
"@type": "Answer",
"text": "Une dysfonction de CYP1A2 peut contribuer à des maladies hépatiques en altérant le métabolisme."
}
},
{
"@type": "Question",
"name": "Comment les complications sont-elles gérées ?",
"position": 23,
"acceptedAnswer": {
"@type": "Answer",
"text": "La gestion des complications implique l'ajustement des traitements et la surveillance étroite."
}
},
{
"@type": "Question",
"name": "Y a-t-il des risques de surdosage avec CYP1A2 ?",
"position": 24,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, un métabolisme altéré peut augmenter le risque de surdosage de certains médicaments."
}
},
{
"@type": "Question",
"name": "Quels sont les effets à long terme de la dysfonction de CYP1A2 ?",
"position": 25,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les effets à long terme peuvent inclure des problèmes de santé chroniques liés au métabolisme."
}
},
{
"@type": "Question",
"name": "Quels facteurs influencent l'activité de CYP1A2 ?",
"position": 26,
"acceptedAnswer": {
"@type": "Answer",
"text": "Des facteurs comme la génétique, l'alimentation et l'usage de médicaments influencent l'activité."
}
},
{
"@type": "Question",
"name": "Comment le tabagisme affecte-t-il CYP1A2 ?",
"position": 27,
"acceptedAnswer": {
"@type": "Answer",
"text": "Le tabagisme induit l'activité de CYP1A2, augmentant le métabolisme de certains médicaments."
}
},
{
"@type": "Question",
"name": "Y a-t-il des risques liés à l'alcool et CYP1A2 ?",
"position": 28,
"acceptedAnswer": {
"@type": "Answer",
"text": "La consommation excessive d'alcool peut inhiber l'activité de CYP1A2, affectant le métabolisme."
}
},
{
"@type": "Question",
"name": "Quels médicaments sont des facteurs de risque pour CYP1A2 ?",
"position": 29,
"acceptedAnswer": {
"@type": "Answer",
"text": "Des médicaments comme les antibiotiques et les antidépresseurs peuvent influencer CYP1A2."
}
},
{
"@type": "Question",
"name": "Comment l'alimentation influence-t-elle CYP1A2 ?",
"position": 30,
"acceptedAnswer": {
"@type": "Answer",
"text": "Certains aliments, comme le pamplemousse, peuvent inhiber ou induire l'activité de CYP1A2."
}
}
]
}
]
}
Expert en Médecine, Optimisation des Parcours de Soins et Révision Médicale
Validation scientifique effectuée le 07/03/2025
Contenu vérifié selon les dernières recommandations médicales
2 publications dans cette catégorie
Affiliations :
Department of Pharmacology, Faculty of Pharmacy, University of Pécs, Rókus u. 2, Pécs H-7624, Hungary; Lab-on-a-Chip Research Group, János Szentágothai Research Centre, University of Pécs, Ifjúság útja 20, Pécs H-7624, Hungary. Electronic address: poor.miklos@pte.hu.
Publications dans "Cytochrome P-450 CYP1A2" :
2 publications dans cette catégorie
Affiliations :
Department of Pharmacology and Experimental Therapeutics, and the Stanley S. Scott Cancer Center, Louisiana State University Health Sciences Center, New Orleans, LA.
Publications dans "Cytochrome P-450 CYP1A2" :
2 publications dans cette catégorie
Affiliations :
Department of Pharmacology and Experimental Therapeutics, and the Stanley S. Scott Cancer Center, Louisiana State University Health Sciences Center, New Orleans, LA.
Publications dans "Cytochrome P-450 CYP1A2" :
2 publications dans cette catégorie
Affiliations :
Department of Pharmacology and Experimental Therapeutics, and the Stanley S. Scott Cancer Center, Louisiana State University Health Sciences Center, New Orleans, LA.
Publications dans "Cytochrome P-450 CYP1A2" :
2 publications dans cette catégorie
Affiliations :
Sichuan Key Laboratory of Animal Genetics and Breeding, Sichuan Animal Science Academy, Chengdu, P.R. China.
Veterinary Natural Medicine Research and GCP Experimental Animal Centre, Lezhi, P.R. China.
Publications dans "Cytochrome P-450 CYP1A2" :
2 publications dans cette catégorie
Affiliations :
Sichuan Key Laboratory of Animal Genetics and Breeding, Sichuan Animal Science Academy, Chengdu, P.R. China.
Veterinary Natural Medicine Research and GCP Experimental Animal Centre, Lezhi, P.R. China.
Publications dans "Cytochrome P-450 CYP1A2" :
2 publications dans cette catégorie
Affiliations :
Sichuan Key Laboratory of Animal Genetics and Breeding, Sichuan Animal Science Academy, Chengdu, P.R. China.
Veterinary Natural Medicine Research and GCP Experimental Animal Centre, Lezhi, P.R. China.
Publications dans "Cytochrome P-450 CYP1A2" :
2 publications dans cette catégorie
Affiliations :
Federal University of Sao Joao del-Rei, Av. Sebastiao Goncalves Coelho, 400, Campus Centro-Oeste, Chanadour, Divinopolis-MG, CEP: 35501-296, Brazil.
Federal University of Minas Gerais, Av. Presidente Antonio Carlos, 667, Campus Pampulha, Belo Horizonte-MG, CEP: 31270-901, Brazil.
Publications dans "Cytochrome P-450 CYP1A2" :
2 publications dans cette catégorie
Affiliations :
Federal University of Sao Joao del-Rei, Av. Sebastiao Goncalves Coelho, 400, Campus Centro-Oeste, Chanadour, Divinopolis-MG, CEP: 35501-296, Brazil.
Publications dans "Cytochrome P-450 CYP1A2" :
2 publications dans cette catégorie
Affiliations :
Federal University of Sao Joao del-Rei, Av. Sebastiao Goncalves Coelho, 400, Campus Centro-Oeste, Chanadour, Divinopolis-MG, CEP: 35501-296, Brazil.
Publications dans "Cytochrome P-450 CYP1A2" :
2 publications dans cette catégorie
Affiliations :
Department of Pharmaceutics, College of Pharmacy, University of Florida, Gainesville, FL 32611, United States.
Publications dans "Cytochrome P-450 CYP1A2" :
2 publications dans cette catégorie
Affiliations :
Federal University of Sao Joao del-Rei, Av. Sebastiao Goncalves Coelho, 400, Campus Centro-Oeste, Chanadour, Divinopolis-MG, CEP: 35501-296, Brazil.
Publications dans "Cytochrome P-450 CYP1A2" :
2 publications dans cette catégorie
Affiliations :
Wuya College of Innovation, Shenyang Pharmaceutical University, Shenyang, Liaoning 110016, P.R. China.
Publications dans "Cytochrome P-450 CYP1A2" :
2 publications dans cette catégorie
Affiliations :
Wuya College of Innovation, Shenyang Pharmaceutical University, Shenyang, Liaoning 110016, P.R. China.
State Key Laboratory of Functions and Applications of Medicinal Plants, Key Laboratory of Pharmaceutics of Guizhou Province, Guizhou Medical University, Guiyang, Guizhou 550025, P.R. China.
Key Laboratory of Environmental Pollution, Monitoring and Disease Control, Ministry of Education, Guizhou Medical University, Guiyang, Guizhou 550025, P.R. China.
Publications dans "Cytochrome P-450 CYP1A2" :
2 publications dans cette catégorie
Affiliations :
Daiichi Sankyo, Inc., Basking Ridge, New Jersey, USA.
Publications dans "Cytochrome P-450 CYP1A2" :
2 publications dans cette catégorie
Affiliations :
Department of Pharmacy, Affiliated Meitan People's Hospital of Zunyi Medical University, Zunyi, Guizhou 564100, P.R. China.
The Key Laboratory of Clinical Pharmacy of Zunyi City, Zunyi Medical University, Zunyi, Guizhou 563006, P.R. China.
Publications dans "Cytochrome P-450 CYP1A2" :
2 publications dans cette catégorie
Affiliations :
The Key Laboratory of Clinical Pharmacy of Zunyi City, Zunyi Medical University, Zunyi, Guizhou 563006, P.R. China.
Laboratory of Stem Cell Regulation with Chinese Medicine and Its Application, Hunan University of Chinese Medicine, Changsha, Hunan 410208, P.R. China.
Publications dans "Cytochrome P-450 CYP1A2" :
2 publications dans cette catégorie
Affiliations :
Department of Neurology, Laboratory of Neurogenetics, University Hospital of Larissa, University of Thessaly, Biopolis, Mezourlo Hill, 41100, Larissa, Greece.
Publications dans "Cytochrome P-450 CYP1A2" :
2 publications dans cette catégorie
Affiliations :
Department of Neurology, Laboratory of Neurogenetics, University Hospital of Larissa, University of Thessaly, Biopolis, Mezourlo Hill, 41100, Larissa, Greece.
Publications dans "Cytochrome P-450 CYP1A2" :
2 publications dans cette catégorie
Affiliations :
Department of Neurology, Laboratory of Neurogenetics, University Hospital of Larissa, University of Thessaly, Biopolis, Mezourlo Hill, 41100, Larissa, Greece.
Publications dans "Cytochrome P-450 CYP1A2" :
Mechanical thrombectomy is a highly effective treatment for acute ischemic stroke caused by large-vessel occlusion in the anterior cerebral circulation, significantly increasing the likelihood of reco...
Diabetic retinopathy (DR) is a serious complication of longstanding type 2 diabetes mellitus (T2DM), a leading cause of blindness and visual disability in the world. The aim of this study is to compar...
Among the T2DM patients enrolled in this study, 26 patients had DR (n = 26) while 29 were without DR (n = 29). The blood and tear samples were obtained from all participants. The level of PAI-1 and tP...
Patients with DR had significantly longer disease duration and higher systolic blood pressure compared to those without DR. Serum PAI-1 level was significantly higher in patients with DR compared to t...
The present study demonstrated a significantly greater serum PAI-1 levels in patients with DR compared to those without DR. No significant correlations between tears and serum PAI-1 and tPA were obser...
LDL Receptor-related Protein-1 (LRP1/CD91) binds diverse ligands, many of which activate cell-signaling. Herein, we compared three LRP1 ligands that inhibit inflammatory responses triggered by lipopol...
Tissue-type plasminogen activator (tPA) is the gold standard for emergency treatment of ischemic stroke, which is the third leading cause of death worldwide. Major challenges of tPA therapy are its ra...
Intracranial hemorrhage (ICH) is the most devastating complication of recombinant tissue plasminogen activator (rtPA) treatment in acute ischemic stroke patients. Data on rtPA-associated asymptomatic ...
To determine the incidence, risk factors, characteristics, management, and clinical outcome of rtPA-associated aICH....
The data were retrieved from the Chiang Mai University Hospital Stroke Registry between 1995 and 2019. Consecutive ischemic stroke patients were included if they were 18 or older and received rtPA. St...
Of 725 rtPA treated patients, 166 (16.0%, 95% confidence interval [CI] 13.4-18.9) had aICH, 50 (6.9%, 95% CI 5.2-9.0) had symptomatic ICH (sICH). Patients with aICH had more hemorrhagic infarctions (H...
The rtPA-associated aICH increased the risk of morbidity and mortality outcomes. Further treatment consensus, guideline generation, or clinical trials focusing on the treatment of rtPA-associated aICH...
Stressful events trigger a set of complex biological responses which follow a bell-shaped pattern. Low-stress conditions have been shown to elicit beneficial effects, notably on synaptic plasticity to...
Fibrinolytic therapy can be effective for management of complex pleural effusions. Tissue plasminogen activator (tPA, 10 mg) and deoxyribonuclease (DNAse) every 12 h with a dwell time of one hour is a...
Charts were reviewed and demographics, clinical data and treatment information were abstracted. Outcomes were assessed based on radiographic findings and need for surgery....
Two hundred and fifteen effusions in 207 patients (8 bilateral) were identified. 85% were either infectious or malignant. Two hundred and forty nine chest tubes were used: 84% were 10 Fr or 12 Fr and ...
Low dose tPA daily with a 12 h dwell time may be as effective as the standard regimen of tPA and DNAse twice daily with one hour dwell. For most patients only three doses were required, and small pigt...
The neurovascular unit (NVU) is assembled by endothelial cells (ECs) and pericytes, and encased by a basement membrane (BM) surveilled by microglia and surrounded by perivascular astrocytes (PVA), whi...
Respiratory system involvement is common in congenital plasminogen deficiency. Although many treatment approaches have been tried, there is still no definitive treatment for respiratory system involve...
We report 2 congenital plasminogen deficiency cases, who presented with severe respiratory symptoms, for whom a novel treatment modality was tried. After intravenous administration of FFP (fresh froze...
Intratracheal administration of tissue plasminogen activator and FFP is an available treatment modality for patients with lung involvement. Fibrin plaques should be carefully removed and new lesion fo...
Ischemic stroke is relatively rare in children, leading to a low level of suspicion and delayed diagnosis, particularly in cases of posterior circulation occlusion when symptoms are less indicative. O...
We report a case of a 16-year-old male who presented to the pediatric emergency department with altered mental status. There was no history of trauma or intoxication. The main symptoms included confus...