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Aldosterone Resistance in Preterm Infants (PREMALDO)

A

Assistance Publique - Hôpitaux de Paris

Status

Completed

Conditions

Newborn

Study type

Observational

Funder types

Other

Identifiers

NCT01176162
P081211
B91017-20 (Other Grant/Funding Number)

Details and patient eligibility

About

In the neonatal period, the human kidney is characterized by a functional immaturity responsible for an impaired ability to regulate water and sodium homeostasis, which is exacerbated by prematurity. This altered sodium handling could be related to a partial renal aldosterone resistance. Renal sodium reabsorption and potassium excretion are mainly controlled by aldosterone, after binding to the mineralocorticoid receptor (MR). The investigators have analyzed MR expression throughout human and mouse renal development, and the investigators found a weak MR expression at birth. The investigators have conducted a pilot study in full-term newborns, which confirmed a partial neonatal aldosterone resistance. This study also highlighted that urinary aldosterone is the best index to accurately assess aldosterone sensitivity at birth.

Full description

Principal objective:

To assess aldosterone resistance at birth by a non invasive measurement of urinary aldosterone, in order to evaluate its intensity as a function of gestational age. Determination of normal values of urinary aldosterone concentration in each group.

Secondary objectives:

Comparison of plasma and urinary electrolytes concentrations with hormonal measurements and clinical parameters. Evolution of these biological parameters throughout the first year of life, depending on gestational age at birth.

Methodology : multicentric study, open study Two hundred-forty newborns will be included in order to constitute 4 groups of 60 children, classified according to their gestational age: < 28 GW, 28 - < 33 GW, 33- < 37 GW, > 37 GW.

Inclusion criteria: every newborn will be included, after written parental consent was obtained.

Study :

Urinary samples will be collected onto a gauze compress, during the first 24 hours of life, at day three, and at 1, 3, 6 and 12 months. A blood sample will be obtained from systematic umbilical cord blood collection at birth and during the Guthrie test at day three. Aldosterone and renin concentrations will be measured in BICETRE Hospital laboratory. Plasma and urinary electrolyte concentrations will be measured in the Biochemistry department. DNA samples will also be gathered from umbilical cord blood for future genetic investigations (functional polymorphisms of the MR gene).

Perspectives This study will permit to assess the intensity of aldosterone resistance in full-term and preterm newborns, by a non invasive method. It should bring new insights into the mechanisms of hormonal regulation of sodium balance in preterm newborns and during the first year of life. Urinary aldosterone assessments may open new perspectives for therapeutic management of water and sodium waste in premature infants.

Enrollment

170 patients

Sex

All

Ages

24 to 41 weeks old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria :

  • Maternal

    • Maternal age ≥ 18 and ≤ 45 years,
    • Written parental consent
    • Normal obstetrical ultrasounds
  • Neonatal - Birth by vaginal delivery or cesarean section

Exclusion criteria :

  • Maternal

    • Type 1 or type 2 diabetes,
    • Adrenal or hypophyseal deficiency
    • Treatment for arterial hypertension
  • Neonatal

    • Perinatal anoxia (defined by an Apgar score < 5 at 5 min and pH < 7,10 and lactacidemia > 9 mmol/l at blood cord).
    • Congenital malformation
    • Chromosomic abnormalities

Trial design

170 participants in 4 patient groups

Group "< 28"
Description:
• Gestational Age \< 28 weeks
Group "28 - < 33"
Description:
• Gestational Age : 28 - \< 33 weeks
Group "33- < 37"
Description:
Gestational Age : 33- \< 37 weeks
Group "> 37"
Description:
Gestational Age \> 37 weeks

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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