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The Interpretation of Bloodspot 17α-Hydroxyprogesterone Levels in Term and Pre-Term Neonates
Author(s) -
Janet Berry,
P R Betts,
Peter J. Wood
Publication year - 1986
Publication title -
annals of clinical biochemistry international journal of laboratory medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.6
H-Index - 80
eISSN - 1758-1001
pISSN - 0004-5632
DOI - 10.1177/000456328602300510
Subject(s) - hydroxyprogesterone , creatinine , endocrinology , medicine , term (time) , sodium , urinary system , chemistry , hormone , steroid , physics , quantum mechanics , organic chemistry
Bloodspot 17α-hydroxyprogesterone, plasma cortisol, plasma sodium and urinary 17α-hydroxyprogesterone, cortisol, sodium and creatinine levels were determined in 24 term and 32 pre-term infants on the third, eighth and fourteenth days of life. Pre-term infants, whether ‘well’ or ‘sick’, had significantly raised bloodspot 17α-hydroxyprogesterone levels (up to 158 nmol/L) compared with those found in term infants (up to 18·8 nmol/L). Urinary 17α-hydroxyprogesterone/creatinine ratios were also higher in pre-term infants. Plasma cortisol results showed similar ranges for term and pre-term infants, and bloodspot 17α-hydroxyprogesterone/plasma cortisol ratios for day 3 specimens correlated with the degree of prematurity. These results may be due either to immature enzyme systems in the pre-term baby or to an excess of related steroids cross-reacting in the 17α-hydroxyprogesterone assay. We propose the use of two distinct upper limits of normal of 20 nmol/L (term infants) and 200 nmol/L (pre-term infants), for the interpretation of bloodspot 17α-hydroxyprogesterone levels at the end of the first week of life.

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