Literature DB >> 3126357

Amniotic fluid propionylcarnitine in methylmalonic aciduria.

D Penn1, E Schmidt-Sommerfeld, C Jakobs, L L Bieber.   

Abstract

Amniotic fluid samples from pregnancies complicated by foetal methylmalonic aciduria and from metabolically normal pregnancies were obtained at 16-18 weeks of gestation and analysed for total, free and acylcarnitine and individual carnitine esters. The amniotic fluid concentrations of total acylcarnitine and propionylcarnitine were higher in pregnancies with higher in pregnancies with methylmalonic aciduria than in normal pregnancies. The predominant carnitine ester was propionylcarnitine in the methylmalonic aciduria group and acetylcarnitine in the normal group. These findings suggest that in methylmalonic aciduria, abnormalities of carnitine metabolism already occur early in gestation. The amount of propionylcarnitine in amniotic fluid may be useful as an additional indicator of foetal methylmalonic aciduria.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3126357     DOI: 10.1007/bf01799980

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  11 in total

1.  An improved and simplified radioisotopic assay for the determination of free and esterified carnitine.

Authors:  J D McGarry; D W Foster
Journal:  J Lipid Res       Date:  1976-05       Impact factor: 5.922

2.  Short-chain acylcarnitines: identification and quantitation.

Authors:  L L Bieber; J Kerner
Journal:  Methods Enzymol       Date:  1986       Impact factor: 1.600

3.  Prenatal diagnosis of the organic acidurias.

Authors:  L Sweetman
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

4.  Acetylcarnitine and free carnitine in body fluids before and after birth.

Authors:  M Novak; P B Wieser; M Buch; P Hahn
Journal:  Pediatr Res       Date:  1979-01       Impact factor: 3.756

5.  Carnitine metabolism and inborn errors.

Authors:  A G Engel; C J Rebouche
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

6.  Propionylcarnitine excretion in propionic and methylmalonic acidurias: a cause of carnitine deficiency.

Authors:  S Di Donato; M Rimoldi; B Garavaglia; G Uziel
Journal:  Clin Chim Acta       Date:  1984-05-16       Impact factor: 3.786

7.  The influence of maternal fat metabolism on fetal carnitine levels.

Authors:  E Schmidt-Sommerfeld; D Penn; H Wolf
Journal:  Early Hum Dev       Date:  1981-07       Impact factor: 2.079

8.  Transfer and metabolism of carnitine and carnitine esters in the in vitro perfused human placenta.

Authors:  E Schmidt-Sommerfeld; D Penn; R J Sodha; M Prögler; M Novak; H Schneider
Journal:  Pediatr Res       Date:  1985-07       Impact factor: 3.756

9.  Possible functions of short-chain and medium-chain carnitine acyltransferases.

Authors:  L L Bieber; R Emaus; K Valkner; S Farrell
Journal:  Fed Proc       Date:  1982-10

10.  [Carnitine in the treatment of methylmalonic aciduria (MMA)].

Authors:  D Penn; H Schmidt; A Otten; E Schmidt-Sommerfeld
Journal:  Monatsschr Kinderheilkd       Date:  1986-10       Impact factor: 0.323

View more
  2 in total

1.  Acylcarnitines in amniotic fluid: application to the prenatal diagnosis of propionic acidaemia.

Authors:  J L Van Hove; D H Chace; S G Kahler; D S Millington
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

2.  A fetus with mitochondrial trifunctional protein deficiency: Elevation of 3-OH-acylcarnitines in amniotic fluid functionally assured the genetic diagnosis.

Authors:  Ryosuke Bo; Yuki Hasegawa; Kenji Yamada; Hironori Kobayashi; Takeshi Taketani; Seiji Fukuda; Seiji Yamaguchi
Journal:  Mol Genet Metab Rep       Date:  2015-12-05
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.