4.1 Article

Acetylcholinesterase activity and bone biochemical markers in premature and full-term neonates

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JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
卷 31, 期 12, 页码 1363-1366

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WALTER DE GRUYTER GMBH
DOI: 10.1515/jpem-2018-0426

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acetylcholinesterase; bone biomarkers; bone metabolism; metabolic bone disease of prematurity; premature infants

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Background: Almost 30% of the premature infants have low body weight and bone mineral density due to prematurity. There is no consensus of screening premature neonates for metabolic bone disease; therefore, it is important to investigate the use of bone biochemical parameters. Latest studies involved the activity of acetylcholinesterase as a mediator in bone remodeling. It is hypothesized that there is a possible correlation of bone biochemical biomarkers and acetylcholinesterase (AChE) activity in premature infants. Methods: We studied 50 neonates (26 preterm with gestational age <32 weeks, 24 full-term). Clinical data (sex, gestational week) and anthropometric parameters (body weight) were recorded. We directly measured the bone biochemical markers in serum such as alkaline phosphatase (ALP), calcium (Ca), phosphorus (P), magnesium (Mg) and parathyroid hormone (PTH). In addition, we measured the AChE activity. Results: ALP and parathyroid hormone levels were higher, but Ca, P and AChE were lower in premature neonates group compared with full-term ones. There is a significant positive correlation of gestational age with body weight, Ca and AChE. A significant negative correlation was observed for ALP and PTH with gestational age. Conclusions: We found a gestational age-related increase of AChE activity. There were significant relationships between AChE activity with P and PTH.

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