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Published in: BMC Pregnancy and Childbirth 1/2020

Open Access 01-12-2020 | Case report

Increased creatine demand during pregnancy in Arginine: Glycine Amidino-Transferase deficiency: a case report

Authors: Maria Grazia Alessandrì, Francesca Strigini, Giovanni Cioni, Roberta Battini

Published in: BMC Pregnancy and Childbirth | Issue 1/2020

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Abstract

Background

Creatine (Cr), an amino acid derivative, is one of the most important sources of energy acting as both a spatial and temporal energy buffer through its phosphorylated analogue phosphocreatine (PCr) and creatine kinase (CK). Maternal Cr biosynthesis and metabolism seem to play an important role in pregnancy, as shown in preclinical and in healthy human pregnancy studies. Patients with Arginine:Glycine Amidino-Transferase deficiency (AGAT-d), due to the deficit of the first enzyme involved in Cr synthesis, are at a disadvantage due to their failure to synthesize Cr and their dependence on external intake, in contrast to normal subjects, where changes in Cr biosynthesis supply their needs.
We report the outcomes of a pregnancy in an AGAT-d woman, and the challenge we faced in managing her treatment with oral Cr to ensure optimal conditions for her fetus.

Case presentation

A 22-year-old AGAT-d woman referred to our Institute for the management of her first conception at 11 weeks of fetal gestational age. Sonographic monitoring at 20 w GA indicated a reduction of fetal growth, in particular of the head circumference that was below the 3rd centile. Biochemical monitoring of Cr in biological fluids of the mother revealed a decline of the Cr concentrations, in particular in the urine sample, requiring prompt correction of the Cr dose. At 35 weeks of gestation the patient delivered a male infant, heterozygous for GATM mutation, with normal brain Cr levels; at one year the baby achieved typical developmental milestones.

Conclusions

This rare pregnancy demonstrates that Cr levels in the blood and urine of the mother with AGAT-d decreased since the first months of gestation. The increase of the Cr daily dose administered to the mother seems to have produced beneficial effects also on the fetus.
Literature
1.
go back to reference Stromberger C, Bodamer O, Stockler-Ipsiroglu S. Clinical characteristics and diagnostic clues in inborn errors of creatine metabolism. J Inher Metab Dis. 2003;26:299–308.CrossRef Stromberger C, Bodamer O, Stockler-Ipsiroglu S. Clinical characteristics and diagnostic clues in inborn errors of creatine metabolism. J Inher Metab Dis. 2003;26:299–308.CrossRef
2.
go back to reference Stockler-Ipsiroglu S, Apatean D, Battini R, DeBrosse S, Dessoffy K, Edvardson S, et al. Arginine:glycine amidinotransferase (AGAT) deficiency: Clinical features and long term outcomes, in 16 patients diagnosed worldwide. Mol Genet Metab. 2015;116:252–9.CrossRef Stockler-Ipsiroglu S, Apatean D, Battini R, DeBrosse S, Dessoffy K, Edvardson S, et al. Arginine:glycine amidinotransferase (AGAT) deficiency: Clinical features and long term outcomes, in 16 patients diagnosed worldwide. Mol Genet Metab. 2015;116:252–9.CrossRef
3.
go back to reference Ellery SJ, LaRosa DA, Kett MM, Della Gatta PA, Snow RJ, Walker DW, et al. Maternal creatine homeostasis is altered during gestation in the spiny mouse: is this a metabolic adaptation to pregnancy? BMC Pregnancy Childbirth. 2015;15:92–100.CrossRef Ellery SJ, LaRosa DA, Kett MM, Della Gatta PA, Snow RJ, Walker DW, et al. Maternal creatine homeostasis is altered during gestation in the spiny mouse: is this a metabolic adaptation to pregnancy? BMC Pregnancy Childbirth. 2015;15:92–100.CrossRef
4.
go back to reference Dickinson H, Davies-Tuck M, Ellery SJ, Grieger JA, Wallace EM, Snow RJ, et al. Maternal creatine in pregnancy: a retrospective cohort study. BJOG. 2016;123:1830–8.CrossRef Dickinson H, Davies-Tuck M, Ellery SJ, Grieger JA, Wallace EM, Snow RJ, et al. Maternal creatine in pregnancy: a retrospective cohort study. BJOG. 2016;123:1830–8.CrossRef
5.
go back to reference Ellery SJ, Della Gatta PA, Bruce CR, Kowalski GM, Davies-Tuck M, Mockler JC, et al. Creatine biosynthesis and transport by the term human placenta. Placenta. 2017;52:86–93.CrossRef Ellery SJ, Della Gatta PA, Bruce CR, Kowalski GM, Davies-Tuck M, Mockler JC, et al. Creatine biosynthesis and transport by the term human placenta. Placenta. 2017;52:86–93.CrossRef
6.
go back to reference Choe C, Nabuurs C, Stockebrand MC, Neu A, Nunes P, Morellini F, et al. L-arginine:glycine amidinotransferase deficiency protects from metabolic syndrome. Hum Mol Genet. 2013;22:110–23.CrossRef Choe C, Nabuurs C, Stockebrand MC, Neu A, Nunes P, Morellini F, et al. L-arginine:glycine amidinotransferase deficiency protects from metabolic syndrome. Hum Mol Genet. 2013;22:110–23.CrossRef
7.
go back to reference Item CB, Stöckler-Ipsiroglu S, Stromberger C, Mühl A, Alessandrì MG, Bianchi MC, et al. Arginine:glycine amidinotransferase deficiency: the third inborn error of creatine metabolism in humans. Am J Hum Genet. 2001;69:1127–33.CrossRef Item CB, Stöckler-Ipsiroglu S, Stromberger C, Mühl A, Alessandrì MG, Bianchi MC, et al. Arginine:glycine amidinotransferase deficiency: the third inborn error of creatine metabolism in humans. Am J Hum Genet. 2001;69:1127–33.CrossRef
8.
go back to reference Battini R, Alessandrì MG, Casalini C, Casarano M, Tosetti M, Cioni G. Fifteen-year follow-up of Italian families affected by arginine glycine amidinotransferase deficiency. Orphanet J Rare Dis. 2017;12:2. Battini R, Alessandrì MG, Casalini C, Casarano M, Tosetti M, Cioni G. Fifteen-year follow-up of Italian families affected by arginine glycine amidinotransferase deficiency. Orphanet J Rare Dis. 2017;12:2.
9.
go back to reference Alessandrì MG, Celati L, Battini R, Casarano M, Cioni G. Gas chromatography/mass spectrometry assay for arginine:glycine-amidinotransferase deficiency. Anal Biochem. 2005;343:356–58.CrossRef Alessandrì MG, Celati L, Battini R, Casarano M, Cioni G. Gas chromatography/mass spectrometry assay for arginine:glycine-amidinotransferase deficiency. Anal Biochem. 2005;343:356–58.CrossRef
10.
go back to reference Hadlock FP, Deter RL, Harrist RB, Park SK. Fetal head circumference: relation to menstrual age. Am J Roentgenol. 1982;138:649–53.CrossRef Hadlock FP, Deter RL, Harrist RB, Park SK. Fetal head circumference: relation to menstrual age. Am J Roentgenol. 1982;138:649–53.CrossRef
11.
go back to reference Pinto J, Barros AS, Domingues MRM, Goodfellow BJ, Galhano E, Pita C, et al. Following Healthy Pregnancy by NMR Metabolomics of Plasma and Correlation to Urine. J Proteome Res. 2015;14:1263–74.CrossRef Pinto J, Barros AS, Domingues MRM, Goodfellow BJ, Galhano E, Pita C, et al. Following Healthy Pregnancy by NMR Metabolomics of Plasma and Correlation to Urine. J Proteome Res. 2015;14:1263–74.CrossRef
12.
go back to reference Evangelou IE, du Plessis AJ, Vezina G, Noeske R, Limperopoulos C. Elucidating Metabolic Maturation in the Healthy Fetal Brain Using 1H-MR Spectroscopy. AJNR. 2016;37:360–6.CrossRef Evangelou IE, du Plessis AJ, Vezina G, Noeske R, Limperopoulos C. Elucidating Metabolic Maturation in the Healthy Fetal Brain Using 1H-MR Spectroscopy. AJNR. 2016;37:360–6.CrossRef
13.
go back to reference Ellery SJ, Murthi P, Davies-Tuck ML, Della Gatta PA, May AK, Kowalski GM, et al. Placental creatine metabolism in cases of placental insufficiency and reduced fetal growth. Mol Hum Reprod. 2019;25:495–505. Ellery SJ, Murthi P, Davies-Tuck ML, Della Gatta PA, May AK, Kowalski GM, et al. Placental creatine metabolism in cases of placental insufficiency and reduced fetal growth. Mol Hum Reprod. 2019;25:495–505.
Metadata
Title
Increased creatine demand during pregnancy in Arginine: Glycine Amidino-Transferase deficiency: a case report
Authors
Maria Grazia Alessandrì
Francesca Strigini
Giovanni Cioni
Roberta Battini
Publication date
01-12-2020
Publisher
BioMed Central
Published in
BMC Pregnancy and Childbirth / Issue 1/2020
Electronic ISSN: 1471-2393
DOI
https://doi.org/10.1186/s12884-020-03192-4

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