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The Development of Circadian Rhythms in Human Infants

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crucial <strong>in</strong> physiological development and maturation. However it should be noted that<br />

the study did not <strong>in</strong>clude extremely premature <strong>in</strong>fants. It <strong>in</strong>cluded only n<strong>in</strong>e <strong>in</strong>fants<br />

born between 31 and 34 weeks gestation. <strong>The</strong> HPA axis <strong>of</strong> extremely premature<br />

<strong>in</strong>fants would be expected to be significantly immature and not likely to mature at a<br />

similar postnatal age to term <strong>in</strong>fants.<br />

<strong>The</strong> visual data were based on work<strong>in</strong>g def<strong>in</strong>itions <strong>of</strong> the appearance <strong>of</strong> a diurnal<br />

pattern <strong>of</strong> secretion for the secretion <strong>of</strong> the hormones melaton<strong>in</strong> and cortisol, sleep<br />

and peripheral gene expression.<br />

Detailed statistical analysis to determ<strong>in</strong>e the exact tim<strong>in</strong>g <strong>of</strong> the maturation <strong>of</strong> each<br />

aspect <strong>of</strong> physiology studied was not feasible due to the sample size, and the <strong>in</strong>herent<br />

difficulties compar<strong>in</strong>g different types <strong>of</strong> outputs. For example it is problematic to<br />

attempt to l<strong>in</strong>k hormone secretion directly to gene expression; whilst compar<strong>in</strong>g age<br />

<strong>of</strong> maturation <strong>of</strong> cortisol secretion with melaton<strong>in</strong> secretion by determ<strong>in</strong><strong>in</strong>g tim<strong>in</strong>g <strong>of</strong><br />

maximal diurnal rhythmicity (as there are both humoral outputs) is more<br />

straightforward. Although there are limitations as to what can be <strong>in</strong>ferred from the<br />

data, there is a possible suggestion that the physiological maturation <strong>of</strong> the different,<br />

but <strong>in</strong>terrelated systems, occurs over a period <strong>of</strong> weeks, rather than simultaneously.<br />

<strong>The</strong> box and whisker plots show there is wide variability with<strong>in</strong> each physiological<br />

system measured for the age at which „maturation‟ took place but does not clearly<br />

give any <strong>in</strong>dication <strong>of</strong> the precision <strong>of</strong> the estimate <strong>of</strong> the mean for each week <strong>of</strong><br />

maturation. This study does, however, contribute strongly towards the argument for<br />

larger studies, to more accurately answer the question whether there is actually a<br />

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