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Phenotypical Approach of the Drug Metabolizing Hormones Activity Before and After Roux-en Y-Gastric Bypass

Phase 1
Completed
Conditions
Obesity
Interventions
Drug: phenotypical approach
Registration Number
NCT01443039
Lead Sponsor
Assistance Publique - Hôpitaux de Paris
Brief Summary

The activity of drug-metabolizing enzymes and transporters evolutes after Roux-en-Y gastric Bypass.

Primary aim : To study the intra individual evolution of phenotypical markers of different drug metabolizing enzymes and one transporter (CYP1A2, CYP2D6, CYP2C9, CYP2C19, CYP3A4 and P-gp), using a cocktail phenotypic approach, after Roux-en-Y gastric Bypass.

Detailed Description

Principal Judgement criteria :

Phenotypical markers of enzymes and transporter activity before, at 5-8 weeks and 25-30 weeks following surgery.

Secondary judgement criteria :

* Genetic polymorphisms known to affect expression and/or activity of enzymes and transporter.

* Intestinal and hepatic expression and activity of the enzymes and transporter of interest.

* Markers of inflammation Methodology, study design : open-labelled monocentric study.

Sample size : It will be a descriptive experimental study involving 12 subjects.

Study design : In centre 1: Inclusion at least 2 weeks prior to surgery (V0)

In centre 2: Three studies of 12 hours each will occur (in addition with the usual clinical and surgical follow up) at three times periods: in the 8 weeks period before surgery (V1), at 5-8 weeks after surgery (V2) and at 25-30 weeks after surgery (V3).

In centre 3: the patients will undergo gastric bypass surgery (corresponding to the usual clinical and surgical follow up) and samples of jejunum and liver will be obtain during the surgery (J0).

Centres 4 and 5 are involved in samples analysis.Hence, patients will attend 3 visits, in addition to the usual clinical and surgical follow-up.

Study duration: 26 months (with duration of inclusion of 18 months)

Duration for a patient: 38 weeks at maximum (8 months)

Investigating center and participating units: one center enrolling the patients and three centers involving in the others investigations.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
11
Inclusion Criteria
  • Patients with morbid obesity (IMC > 40 kg/m²) or severe obesity (IMC=35-40 kg/m²) with co morbidities (sleep apnea syndrome or hypertension without treatment or steatosis hepatitis) candidates for a gastric bypass.
  • Patient not receiving more than two treatments whose effect on the expression of enzymes and drug transporters is zero other than vitamins.
  • Patient agreeing to participate at three studies of one day (12 hours) occurring at three different periods.
  • Patients aged between 18 and 60 years old.
  • Patient giving its well-informed and free consent.
  • Patient without allergy to any of the drugs used for test.
  • Patients living in France during the study and with French social security
Exclusion Criteria
  • Tabacco
  • Contraception including estrogens compounds
  • Medication other than vitamins.
  • Allergy

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
phenotypical approachphenotypical approachphenotypical approach
Primary Outcome Measures
NameTimeMethod
Phenotypical markers of enzymes and transporter activity25-30 weeks

plasmatic \[Paraxanthine/caffeine\] ratio (T4H) at 25-30 weeks following surgery. - plasmatic \[Omeprazole/5-hydroxyomeprazole\] ratio (T4H) at 25-30 weeks following surgery. - urinary Log (dextromethorphan/dextrorphan) (T0-T8h) at 25-30 weeks following surgery. - urinary Losartan/ E-3174 (T0-8h) at 25-30 weeks following surgery. - plasmatic AUC 0-inf midazolam at 25-30 weeks following surgery. - plasmatic AUC 0-inf digoxin at 25-30 weeks following surgery

Secondary Outcome Measures
NameTimeMethod
Intestinal and hepatic expression and activity of the enzymes and transporter of interest and markers of inflammationbefore surgery

Intestinal and hepatic expression and activity of the enzymes and transporter of interest and markers of inflammation

Trial Locations

Locations (1)

Unit of internal medicine A, Lariboisière Hospital

🇫🇷

Paris, France

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