Antidepressants During Pregnancy and Lactation: Pharmacokinetics and Clinical Implications
Background: The childbearing years are a time of increased vulnerability to the onset of mood disorders in women and a high prevalence of exposure to antidepressant drugs during pregnancy and postpartum has been reported. However, the lack of information regarding the milk transfer and the safety of these drugs in breastfed infants and the related fear of adverse events for the sucking infant are some of the factors responsible for stopping prematurely breast-feeding or avoiding drug therapy. Selective serotonin reuptake inhibitors (SSRI) and selective serotonin and noradrenaline reuptake inhibitors (SNRI) are the most frequently prescribed antidepressant drugs during pregnancy and the post-partum period. They exhibit a wide interpatient variability in their concentration profiles that has been related to numerous environmental, stereochemical, demographic and genetic influences that might alter the level of exposure of breastfed newborns. Limited information is available regarding the safety of use of these antidepressant drugs during lactation, and is generally derived from small studies. A comprehensive description of their distribution and quantification in milk in a larger cohort of patients under various influences and the resulting impact on milk concentrations is lacking.
Objectives: The current proposal addresses the primary objectives of quantifying the range of concentration to citalopram, escitalopram, sertraline, fluoxetine, paroxetine, fluvoxamine, duloxetine and venlafaxine in mother plasma and breast milk in relation to genetic polymorphisms, stereochemistry, demographics and environmental factors in a large cohort of depressive mothers. This will enable to derive the exposure to the breast-fed child taking into account this variability and therefore better adjust treatment to potential influences. As secondary objectives, we will examine the neurodevelopmental outcome of a sub-set of infants subjected to SSRI/SNRI in utero and/or during breastfeeding at birth, 6, 18 and 36 months, and compared to that of a control population of infants not subjected to this treatment.
Expected Results: The proposed strategy will offer new information regarding the expected level of drug exposure associated with each or with a combination of risk factors and help for optimizing the security and rationalizing the use of antidepressant treatment in lactating women. Hence, research on the safety of use of these drugs for the developing child is an area of great public health significance.
|Study Design:||Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
|Official Title:||Antidepressant Treatments During Pregnancy and Lactation: Prediction of Drug Exposure Through Breastfeeding and Evaluation of Drug Effect on the Neonatal Adaptation and the Development of the Young Child|
- Evaluate the pharmacokinetics of SSRI/SNRI antidepressant drugs in breast milk secretion [ Time Frame: week 1 and week 4-6 postpartum ]
The principal aim is to derive exposure to the breast-fed child by simulation while integrating influencing factors on pharmacokinetics (as genetic polymorphism, stereochemistry, demographics or environmental aspects).
5ml blood, 10ml fore-milk and 10ml hind-milk are taken from the mother during the same feed at week 1 and week 4-6 postpartum. Antidepressant drug concentrations are determined by LC-MS/MS and milk composition by human milk analyzer.Pharmacogenetic tests are performed with PCR-Taqman on maternal blood samples and cover genes involved in the metabolism (e.g CYP) and distribution (e.g. p-Gp) of antidepressants. Simulation of antidepressant drug secretion into breast milk will take into account all this information and will be performed with non-linear mixed effects modelling techniques.
- Examine neonatal adaptation [ Time Frame: delivery and week 1 postpartum ]
The specific aim is to evaluate neonatal adaptation after in utero exposure to antidepressants and its relation to cord blood concentration.
5ml blood are taken from the umbilical cord and the mother at delivery. Antidepressant drug concentrations are determined by LC-MS/MS. Finnegan Score is used to evaluate the severity of possible withdrawal or discontinuation syndrome in exposed newborns.
- Examine neurodevelopment [ Time Frame: week 1, month 6, 18 and 36 postpartum ]
The specific aim is to evaluate neurodevelopment of a sub-set of infants exposed to any SSRI/SNRI in utero and/or during breastfeeding compared to a control population of infants not exposed to this treatment.
During week 1 postpartum, somatic and neurologic state of the newborn are evaluated by a pediatrician using routine measures as well as specific tools (Dubowitz's neurologic assessment, Prechtl's general movements). At month 6,18 and 36, neurodevelopment of the infants are assessed using Hammersmith Infant Neurological Examination and Bayley Scales of Infant Development III. At the same time, mother's mental well-being is determined by using self-administered questionnaires (Edinburgh Postnatal Depression Scale, State-Trait Anxiety Inventory, Parental Sens of Competence and Revised Infant Temperament Questionnaire).
- Study of growth [ Time Frame: birth, month 6, 18 and 36 postpartum ]
The specific aim is to evaluate growth of infants exposed to any of the SSRI/SNRI commercialized, compared to standardized growth charts.
Usual infant growth information (size, body weight, head circumference) are collected routinely at birth and month 6,18,36.
- Examine early mother-infant relationship [ Time Frame: Month 6 postpartum ]
The specific aim is to explore the quality of early mother-infant relationship of a sub-set of infants whose mothers are treated with SSRI/SNRI, compared to that of a control population of infants not exposed to this treatment.
At month 6 postpartum, mother-infant relationship is evaluated by pedopsychiatrists using Care Index.
|Study Start Date:||August 2012|
|Estimated Study Completion Date:||December 2018|
|Estimated Primary Completion Date:||December 2016 (Final data collection date for primary outcome measure)|
No Intervention: Control
Pregnant and/or nursing mothers not taking a SSRI or SNRI antidepressant are recruited in a non-exposed group (Control or no SSRI/SNRI). Control group participates only in the sub-studies related to neonatal adaptation, neurodevelopment, growth and early mother-infant relationship.
Experimental: SSRI/SNRI exposure
Pregnant and/or nursing mothers under SSRI or SNRI treatment are recruited in an exposed group (SSRI/SNRI exposure). Drug regimen including dosage, frequency and duration is not modified by the study.
Exposed group of mothers taking one of the mentioned antidepressant drugs of the class of selective serotonin reuptake inhibitors (SSRI) or serotonin/noradrenalin reuptake inhibitors (SNRI).
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01796132
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01796132
|Contact: Chantal Csajka, Prof PhD||0041 21 314 42 firstname.lastname@example.org|
|Contact: Alice Panchaud, PhD||0041 21 314 42 email@example.com|
|Service d'Obstétrique, Service de Néonatologie; Centre Hospitalier Universitaire Nancy||Recruiting|
|Nancy, Meurthe-et-Moselle, France|
|Contact: Jean-Michel Hascoët, Prof MD firstname.lastname@example.org|
|Principal Investigator: Jean-Michel Hascoët, Prof MD|
|Sub-Investigator: Catherine Lamy, MD|
|Service d'Obstétrique, Service de Néonatologie; Hospices civiles de Lyon (HCL)||Recruiting|
|Lyon, Rhône, France|
|Contact: Olivier Claris, Prof MD email@example.com|
|Principal Investigator: Olivier Claris, Prof MD|
|Sub-Investigator: Pascal Gaucherand, Prof MD|
|Sub-Investigator: Etienne Beaufils, MD|
|Sub-Investigator: Kim NGuyen, MD|
|Division de Pharmacologie Clinique, Service d'Obstétrique, Service de Néonatologie, Service de Pédopsychiatrie de liaison, Unité de Pharmacogénétique et Psychopharmacologie Clinique; Centre Hospitalier Universitaire Vaudois (CHUV)||Recruiting|
|Lausanne, Vaud, Switzerland|
|Contact: Chantal Csajka, Prof PhD firstname.lastname@example.org|
|Principal Investigator: Chantal Csajka, Prof PhD|
|Sub-Investigator: Alice Panchaud, PhD|
|Sub-Investigator: Chin B Eap, Prof PhD|
|Sub-Investigator: Jean-Francois Tolsa, Prof MD|
|Sub-Investigator: Yvan Vial, MD MER|
|Sub-Investigator: Myriam Bickle Graz, MD|
|Sub-Investigator: Mathilde Morisod Harari, MD|
|Sub-Investigator: Céline Fischer, MD|
|Service d'Obstétrique, Service de Pédiatrie; Ensemble Hospitalier de la Côte (EHC)||Recruiting|
|Morges, Vaud, Switzerland|
|Contact: Sylvie Rouiller, MD email@example.com|
|Principal Investigator: Sylvie Rouiller, MD|
|Service d'Obstétrique, Service du Développement et de la Croissance; Hopitaux Universitaires Genevois (HUG)||Recruiting|
|Contact: Manuella Epiney, MD firstname.lastname@example.org|
|Principal Investigator: Manuella Epiney, MD|
|Principal Investigator: Cristina Borradori Tolsa, MD|
|Principal Investigator:||Chantal Csajka, Prof PhD||Centre Hospitalier Universitaire Vaudois (CHUV)|