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      Neonatal cardiac hypertrophy: the role of hyperinsulinism—a review of literature

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          Abstract

          Hypertrophic cardiomyopathy (HCM) in neonates is a rare and heterogeneous disorder which is characterized by hypertrophy of heart with histological and functional disruption of the myocardial structure/composition. The prognosis of HCM depends on the underlying diagnosis. In this review, we emphasize the importance to consider hyperinsulinism in the differential diagnosis of HCM, as hyperinsulinism is widely associated with cardiac hypertrophy (CH) which cannot be distinguished from HCM on echocardiographic examination. We supply an overview of the incidence and treatment strategies of neonatal CH in a broad spectrum of hyperinsulinemic diseases. Reviewing the literature, we found that CH is reported in 13 to 44% of infants of diabetic mothers, in approximately 40% of infants with congenital hyperinsulinism, in 61% of infants with leprechaunism and in 48 to 61% of the patients with congenital generalized lipodystrophy. The correct diagnosis is of importance since there is a large variation in prognoses and there are various strategies to treat CH in hyperinsulinemic diseases.

          Conclusion: The relationship between CH and hyperinsulism has implications for clinical practice as it might help to establish the correct diagnosis in neonates with cardiac hypertrophy which has both prognostic and therapeutic consequences. In addition, CH should be recognized as a potential comorbidity which might necessitate treatment in all neonates with known hyperinsulinism.

          What is Known:

          Hyperinsulinism is currently not acknowledged as a cause of hypertrophic cardiomyopathy (HCM) in textbooks and recent Pediatric Cardiomyopathy Registry publications.

          What is New:

          This article presents an overview of the literature of hyperinsulinism in neonates and infants showing that hyperinsulinism is associated with cardiac hypertrophy (CH) in a broad range of hyperinsulinemic diseases.

          As CH cannot be distinguished from HCM on echocardiographic examination, we emphasize the importance to consider hyperinsulinism in the differential diagnosis of HCM/CH as establishing the correct diagnosis has both prognostic and therapeutic consequences.

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          Most cited references95

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          Germline mutations in HRAS proto-oncogene cause Costello syndrome.

          Costello syndrome is a multiple congenital anomaly and mental retardation syndrome characterized by coarse face, loose skin, cardiomyopathy and predisposition to tumors. We identified four heterozygous de novo mutations of HRAS in 12 of 13 affected individuals, all of which were previously reported as somatic and oncogenic mutations in various tumors. Our observations suggest that germline mutations in HRAS perturb human development and increase susceptibility to tumors.
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            Distinct and overlapping functions of insulin and IGF-I receptors.

            Targeted gene mutations have established distinct, yet overlapping, developmental roles for receptors of the insulin/IGF family. IGF-I receptor mediates IGF-I and IGF-II action on prenatal growth and IGF-I action on postnatal growth. Insulin receptor mediates prenatal growth in response to IGF-II and postnatal metabolism in response to insulin. In rodents, unlike humans, insulin does not participate in embryonic growth until late gestation. The ability of the insulin receptor to act as a bona fide IGF-II-dependent growth promoter is underscored by its rescue of double knockout Igf1r/Igf2r mice. Thus, IGF-II is a true bifunctional ligand that is able to stimulate both insulin and IGF-I receptor signaling, although with different potencies. In contrast, the IGF-II/cation-independent mannose-6-phosphate receptor regulates IGF-II clearance. The growth retardation of mice lacking IGF-I and/or insulin receptors is due to reduced cell number, resulting from decreased proliferation. Evidence from genetically engineered mice does not support the view that insulin and IGF receptors promote cellular differentiation in vivo or that they are required for early embryonic development. The phenotypes of insulin receptor gene mutations in humans and in mice indicate important differences between the developmental roles of insulin and its receptor in the two species.
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              Perspective on the Genetics and Diagnosis of Congenital Hyperinsulinism Disorders.

              Congenital hyperinsulinism (HI) is the most common cause of hypoglycemia in children. The risk of permanent brain injury in infants with HI continues to be as high as 25-50% due to delays in diagnosis and inadequate treatment. Congenital HI has been described since the birth of the JCEM under various terms, including "idiopathic hypoglycemia of infancy," "leucine-sensitive hypoglycemia," or "nesidioblastosis."

                Author and article information

                Contributors
                n.d.paauw-2@umcutrecht.nl
                r.stegeman@umcutrecht.nl
                j.termote@umcutrecht.nl
                freund.matthias@klinikum-oldenburg.de
                h.breur@umcutrecht.nl
                Journal
                Eur J Pediatr
                Eur. J. Pediatr
                European Journal of Pediatrics
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0340-6199
                1432-1076
                16 December 2019
                16 December 2019
                2020
                : 179
                : 1
                : 39-50
                Affiliations
                [1 ]GRID grid.7692.a, ISNI 0000000090126352, Department of Obstetrics, Wilhelmina Children’s Hospital Birth Center, , University Medical Center Utrecht, ; Utrecht, The Netherlands
                [2 ]GRID grid.7692.a, ISNI 0000000090126352, Department of Pediatric Cardiology, Wilhelmina Children’s Hospital, , University Medical Center Utrecht, ; PO Box 85090, 3508 AB Utrecht, The Netherlands
                [3 ]GRID grid.7692.a, ISNI 0000000090126352, Department of Pediatric Endocrinology, Wilhelmina Children’s Hospital, , University Medical Center Utrecht, ; Utrecht, The Netherlands
                [4 ]GRID grid.7692.a, ISNI 0000000090126352, Department of Neonatology, Wilhelmina Children’s Hospital Birth Center, , University Medical Center Utrecht, ; Utrecht, The Netherlands
                [5 ]GRID grid.5560.6, ISNI 0000 0001 1009 3608, Department of Pediatric Cardiology, Klinikum Oldenburg, , University of Oldenburg, ; Oldenburg, Germany
                Author notes

                Communicated by Peter de Winter

                Author information
                http://orcid.org/0000-0002-4915-7127
                Article
                3521
                10.1007/s00431-019-03521-6
                6942572
                31840185
                a64655a4-3f40-44ec-ae57-05a01a34122c
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 9 August 2019
                : 30 October 2019
                : 31 October 2019
                Funding
                Funded by: Utrecht University
                Categories
                Review
                Custom metadata
                © Springer-Verlag GmbH Germany, part of Springer Nature 2020

                Pediatrics
                hypertrophic cardiomyopathy,cardiac hypertrophy,hyperinsulinemia,hyperinsulinemic state

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