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Mathematical models of body heat exchanges can be used to define the thermal limits needed to protect premature neonates nursed in incubators against thermal stress–stress that can have potentially devastating impairments on neurological development and body growth. Predictive models can help caregivers to keep a neonate’s body temperature within the normal range and to solve problems that arise during intensive care, such as the risk of hyperthermia during phototherapy, the risk of hypothermia during transport from one clinical centre to another, and the use of a plastic bag to reduce skin water loss and body dehydration. Here, we review the strengths and limitations of models used to predict the risk of thermal stress, with a focus on uncertainties in the algorithms governing heat transfers between the neonate’s skin and the complicated thermal environment encountered in incubators. We describe attempts to reduce the large number of empirical assumptions and uncertainties in this field, and suggest ways of more accurately modelling optimal thermal conditions for neonates nursed in closed incubators.

Spinal muscular atrophy (SMA) is caused by insufficient levels of the survival motor neuron (SMN) protein leading to muscle paralysis and respiratory failure. In mouse, introducing the human SMN2 gene partially rescues Smn-/- embryonic lethality. However current models were either too severe or nearly unaffected precluding convenient drug testing for SMA. We report here new SMN2;Smn-/- lines carrying one to four copies of the human SMN2 gene. Mice carrying three SMN2 copies exhibited an intermediate phenotype with delayed appearance of motor defects and developmental breathing disorders reminiscent of those found in severe SMA patients. Although normal at birth, at 7 days of age respiratory rate was decreased and apnea frequency was increased in SMA mice in parallel with the appearance of neuromuscular junction defects in the diaphragm. With median survival of 15 days and postnatal onset of neurodegeneration, these mice could be an important tool for evaluating new therapeutics.