Management of Dysglycemia in a Pregnancy Complicated by Fanconi–Bickel Syndrome

Background/Objective: Fanconi–Bickel Syndrome (FBS) is an inherited disorder of glucose metabolism resulting from functional loss of glucose transporter 2 characterized by fasting hypoglycemia oscillating with postprandial hyperglycemia. Dysglycemia treatment strategies during FBS pregnancy have not...

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Main Authors: Emily D. Szmuilowicz, MD, MS, Ellen Fruzyna, BS, Nigel Madden, MD, Janelle R. Bolden, MD, Anne Kozek, RD, Erika Vucko, APRN-NP, FNP, Cybele Ghossein, MD, Grant Barish, MD
Format: Article
Language:English
Published: Elsevier 2024-11-01
Series:AACE Clinical Case Reports
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Online Access:http://www.sciencedirect.com/science/article/pii/S2376060524000774
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author Emily D. Szmuilowicz, MD, MS
Ellen Fruzyna, BS
Nigel Madden, MD
Janelle R. Bolden, MD
Anne Kozek, RD
Erika Vucko, APRN-NP, FNP
Cybele Ghossein, MD
Grant Barish, MD
author_facet Emily D. Szmuilowicz, MD, MS
Ellen Fruzyna, BS
Nigel Madden, MD
Janelle R. Bolden, MD
Anne Kozek, RD
Erika Vucko, APRN-NP, FNP
Cybele Ghossein, MD
Grant Barish, MD
author_sort Emily D. Szmuilowicz, MD, MS
collection DOAJ
description Background/Objective: Fanconi–Bickel Syndrome (FBS) is an inherited disorder of glucose metabolism resulting from functional loss of glucose transporter 2 characterized by fasting hypoglycemia oscillating with postprandial hyperglycemia. Dysglycemia treatment strategies during FBS pregnancy have not been reported, and insulin therapy carries significant risk due to fasting hypoglycemia in FBS. We report for the first time: (1) glycemic profiles obtained via continuous glucose monitoring (CGM), (2) CGM-guided strategies for cornstarch and nutritional therapy for fasting hypoglycemia and postprandial hyperglycemia, respectively, and (3) placental glucose transporter 2 isoform expression in a pregnant individual with FBS. Case Report: A 27-year-old woman with FBS presented at 6 weeks gestation for management of fasting hypoglycemia and postprandial hyperglycemia. Cornstarch therapy for fasting hypoglycemia and nutritional therapy for postprandial hyperglycemia were iteratively adjusted across gestation based on CGM-derived glycemic patterns. Pregnancy-specific glycemic targets were successfully achieved, and she delivered a healthy term infant. Glucose transporter 2 isoform was not detected in placental tissue. Discussion: We report for the first time glycemic patterns across gestation in a pregnant individual with FBS. Glycemic targets were achieved through stepwise optimization of nutritional and cornstarch therapy, both guided by CGM data. Our approach obviated the need for insulin therapy, which carries amplified risk in FBS. Conclusion: Fasting hypoglycemia and postprandial hyperglycemia can be effectively treated through CGM-guided adjustment of both nutritional and glucose polymer therapies in FBS pregnancy. More broadly, our case highlights a novel application for CGM in the management of uncommon glucose metabolism disorders during pregnancy.
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spelling doaj-art-9aceabc1bd8e4a07a26c0c6afd57d00e2024-12-11T05:57:00ZengElsevierAACE Clinical Case Reports2376-06052024-11-01106224228Management of Dysglycemia in a Pregnancy Complicated by Fanconi–Bickel SyndromeEmily D. Szmuilowicz, MD, MS0Ellen Fruzyna, BS1Nigel Madden, MD2Janelle R. Bolden, MD3Anne Kozek, RD4Erika Vucko, APRN-NP, FNP5Cybele Ghossein, MD6Grant Barish, MD7Division of Endocrinology, Metabolism, and Molecular Medicine, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois; Address correspondence to Dr Emily D. Szmuilowicz, Division of Endocrinology, Metabolism, and Molecular Medicine, Department of Medicine, Northwestern University Feinberg School of Medicine, 645 N. MI Ave, Suite 530, Chicago, Illinois.Division of Endocrinology, Metabolism, and Molecular Medicine, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IllinoisDivision of Maternal-Fetal Medicine, Department of Obstetrics & Gynecology, Northwestern University Feinberg School of Medicine, Chicago, IllinoisDivision of Maternal-Fetal Medicine, Department of Obstetrics & Gynecology, Northwestern University Feinberg School of Medicine, Chicago, IllinoisDivision of Pediatric Genetics, Genomics and Metabolism, Ann & Robert H. Lurie Children’s Hospital of Chicago, Chicago, IllinoisDivision of Pediatric Genetics, Genomics and Metabolism, Ann & Robert H. Lurie Children’s Hospital of Chicago, Chicago, IllinoisDivision of Nephrology and Hypertension, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IllinoisDivision of Endocrinology, Metabolism, and Molecular Medicine, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois; Division of Endocrinology, Diabetes, and Metabolism, Jesse Brown VA Medical Center, Chicago, IllinoisBackground/Objective: Fanconi–Bickel Syndrome (FBS) is an inherited disorder of glucose metabolism resulting from functional loss of glucose transporter 2 characterized by fasting hypoglycemia oscillating with postprandial hyperglycemia. Dysglycemia treatment strategies during FBS pregnancy have not been reported, and insulin therapy carries significant risk due to fasting hypoglycemia in FBS. We report for the first time: (1) glycemic profiles obtained via continuous glucose monitoring (CGM), (2) CGM-guided strategies for cornstarch and nutritional therapy for fasting hypoglycemia and postprandial hyperglycemia, respectively, and (3) placental glucose transporter 2 isoform expression in a pregnant individual with FBS. Case Report: A 27-year-old woman with FBS presented at 6 weeks gestation for management of fasting hypoglycemia and postprandial hyperglycemia. Cornstarch therapy for fasting hypoglycemia and nutritional therapy for postprandial hyperglycemia were iteratively adjusted across gestation based on CGM-derived glycemic patterns. Pregnancy-specific glycemic targets were successfully achieved, and she delivered a healthy term infant. Glucose transporter 2 isoform was not detected in placental tissue. Discussion: We report for the first time glycemic patterns across gestation in a pregnant individual with FBS. Glycemic targets were achieved through stepwise optimization of nutritional and cornstarch therapy, both guided by CGM data. Our approach obviated the need for insulin therapy, which carries amplified risk in FBS. Conclusion: Fasting hypoglycemia and postprandial hyperglycemia can be effectively treated through CGM-guided adjustment of both nutritional and glucose polymer therapies in FBS pregnancy. More broadly, our case highlights a novel application for CGM in the management of uncommon glucose metabolism disorders during pregnancy.http://www.sciencedirect.com/science/article/pii/S2376060524000774Fanconi–Bickel Syndromepregnancyglucose transporter 2continuous glucose monitoringcornstarch therapy
spellingShingle Emily D. Szmuilowicz, MD, MS
Ellen Fruzyna, BS
Nigel Madden, MD
Janelle R. Bolden, MD
Anne Kozek, RD
Erika Vucko, APRN-NP, FNP
Cybele Ghossein, MD
Grant Barish, MD
Management of Dysglycemia in a Pregnancy Complicated by Fanconi–Bickel Syndrome
AACE Clinical Case Reports
Fanconi–Bickel Syndrome
pregnancy
glucose transporter 2
continuous glucose monitoring
cornstarch therapy
title Management of Dysglycemia in a Pregnancy Complicated by Fanconi–Bickel Syndrome
title_full Management of Dysglycemia in a Pregnancy Complicated by Fanconi–Bickel Syndrome
title_fullStr Management of Dysglycemia in a Pregnancy Complicated by Fanconi–Bickel Syndrome
title_full_unstemmed Management of Dysglycemia in a Pregnancy Complicated by Fanconi–Bickel Syndrome
title_short Management of Dysglycemia in a Pregnancy Complicated by Fanconi–Bickel Syndrome
title_sort management of dysglycemia in a pregnancy complicated by fanconi bickel syndrome
topic Fanconi–Bickel Syndrome
pregnancy
glucose transporter 2
continuous glucose monitoring
cornstarch therapy
url http://www.sciencedirect.com/science/article/pii/S2376060524000774
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