Parenteral nutrition compromises neurodevelopment of preterm pigs

J Nutr. 2014 Dec;144(12):1920-7. doi: 10.3945/jn.114.197145. Epub 2014 Oct 23.

Abstract

Background: Despite advances in nutritional support and intensive care, preterm infants are at higher risk of compromised neurodevelopment.

Objective: This study evaluated the contribution of total parenteral nutrition (PN) to compromised neurodevelopment after preterm birth.

Methods: Preterm pigs were provided PN or enteral nutrition (EN) for 10 d. Neurodevelopment was assessed by observations of motor activity and evaluation of sensory/motor reflexes, brain weight, MRI, and cerebellar histology.

Results: Despite similar gains in body weight, PN pigs had smaller brains (32 ± 0.4 vs. 35 ± 0.6 g; P = 0.0002) including the cerebellum, as well as reduced motor activity (P = 0.005), which corresponded to underdeveloped myelination (P = 0.004) measured by diffusion tensor imaging. PN resulted in lower serum triglycerides (17 ± 5.9 vs. 27 ± 3.1 mg/dL; P = 0.05), total cholesterol (31 ± 9.6 vs. 85 ± 8.1 mg/dL; P = 0.04), VLDL cholesterol (3.7 ± 1.2 vs. 5.7 ± 0.7 mg/dL; P = 0.04), and HDL cholesterol (16 ± 4.6 vs. 57 ± 7.3 mg/dL; P = 0.03) and nonsignificantly lower LDL cholesterol (10.7 ± 4.4 vs. 22.7 ± 2.9 mg/dL; P = 0.09).

Conclusions: The compromised neurodevelopment caused by total PN is a novel finding, was independent of confounding variables (disease, inconsistent gestational ages, diverse genetics, extrauterine growth retardation, and inconsistent neonatal intensive care unit protocols), and highlights a need to improve current PN solutions. The preterm pig is a translational animal model for improving nutrition support to enhance neurodevelopment of preterm infants requiring PN.

Keywords: animal model; brain; gestation; infant; premature.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine Transaminase / blood
  • Alkaline Phosphatase / blood
  • Animals
  • Animals, Newborn
  • Aspartate Aminotransferases / blood
  • Behavior, Animal / drug effects
  • Bilirubin / blood
  • Blood Glucose / metabolism
  • Brain / drug effects
  • Brain / growth & development*
  • Cholesterol, HDL / blood
  • Cholesterol, LDL / blood
  • Creatinine / blood
  • Enteral Nutrition
  • Gestational Age
  • Magnetic Resonance Imaging
  • Models, Animal
  • Neurons / drug effects*
  • Neurons / metabolism
  • Parenteral Nutrition / adverse effects*
  • Serum Albumin / metabolism
  • Swine
  • Triglycerides / blood

Substances

  • Blood Glucose
  • Cholesterol, HDL
  • Cholesterol, LDL
  • Serum Albumin
  • Triglycerides
  • Creatinine
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Alkaline Phosphatase
  • Bilirubin