Bringing precision medicine to the management of pregnancy in women with glucokinase-MODY: a study of diagnostic accuracy and feasibility of non-invasive prenatal testing.
dc.contributor.author | Hughes, AE | |
dc.contributor.author | Houghton, JAL | |
dc.contributor.author | Bunce, B | |
dc.contributor.author | Chakera, AJ | |
dc.contributor.author | Spyer, G | |
dc.contributor.author | Shepherd, MH | |
dc.contributor.author | Flanagan, SE | |
dc.contributor.author | Hattersley, AT | |
dc.date.accessioned | 2023-09-15T09:08:22Z | |
dc.date.issued | 2023-08-31 | |
dc.date.updated | 2023-09-14T16:04:57Z | |
dc.description.abstract | AIMS/HYPOTHESIS: In pregnancies where the mother has glucokinase-MODY (GCK-MODY), fetal growth is determined by fetal genotype. When the fetus inherits a maternal pathogenic GCK variant, normal fetal growth is anticipated, and insulin treatment of maternal hyperglycaemia is not recommended. At present, fetal genotype is estimated from measurement of fetal abdominal circumference on ultrasound. Non-invasive prenatal testing of fetal GCK genotype (NIPT-GCK) using cell-free DNA in maternal blood has recently been developed. We aimed to compare the diagnostic accuracy of NIPT-GCK with that of ultrasound, and determine the feasibility of using NIPT-GCK to guide pregnancy management. METHODS: We studied an international cohort of pregnant women with hyperglycaemia due to GCK-MODY. We compared the diagnostic accuracy of NIPT-GCK with that of measurement of fetal abdominal circumference at 28 weeks' gestation (n=38) using a directly genotyped offspring sample as the reference standard. In a feasibility study, we assessed the time to result given to clinicians in 43 consecutive pregnancies affected by GCK-MODY between July 2019 and September 2021. RESULTS: In terms of diagnostic accuracy, NIPT-GCK was more sensitive and specific than ultrasound in predicting fetal genotype (sensitivity 100% and specificity 96% for NIPT-GCK vs sensitivity 53% and specificity 61% for fetal abdominal circumference 75th percentile). In terms of feasibility, a valid NIPT-GCK fetal genotype (≥95% probability) was reported in all 38 pregnancies with an amenable variant and repeated samples when needed. The median time to report was 5 weeks (IQR 3-8 weeks). For the 25 samples received before 20 weeks' gestation, results were reported at a median gestational age of 20 weeks (IQR 18-24), with 23/25 (92%) reported before 28 weeks. CONCLUSIONS/INTERPRETATION: Non-invasive prenatal testing of fetal genotype in GCK-MODY pregnancies is highly accurate and is capable of providing a result before the last trimester for most patients. This means that non-invasive prenatal testing of fetal genotype is the optimal approach to management of GCK-MODY pregnancies. | en_GB |
dc.description.sponsorship | Wellcome Trust | en_GB |
dc.description.sponsorship | Wellcome Trust | en_GB |
dc.description.sponsorship | National Institute for Health Research (NIHR) | en_GB |
dc.format.extent | 1-10 | |
dc.format.medium | Print-Electronic | |
dc.identifier.citation | Published online 31 August 2023 | en_GB |
dc.identifier.doi | https://doi.org/10.1007/s00125-023-05982-9 | |
dc.identifier.grantnumber | 223187/Z/21/Z/WT | en_GB |
dc.identifier.grantnumber | WT203918/WT | en_GB |
dc.identifier.grantnumber | NIHR4-SNMRL058 | en_GB |
dc.identifier.uri | http://hdl.handle.net/10871/133996 | |
dc.identifier | ORCID: 0000-0003-1352-4447 (Hughes, Alice E) | |
dc.identifier | ScopusID: 55882698900 (Hughes, Alice E) | |
dc.identifier | ORCID: 0000-0002-8670-6340 (Flanagan, Sarah E) | |
dc.identifier | ScopusID: 13408960500 (Flanagan, Sarah E) | |
dc.identifier | ORCID: 0000-0001-5620-473X (Hattersley, Andrew T) | |
dc.language.iso | en | en_GB |
dc.publisher | Springer | en_GB |
dc.relation.url | https://www.ncbi.nlm.nih.gov/pubmed/37653058 | en_GB |
dc.relation.url | https://www.diabetesge nes.org/current-research/gck-mody-nipt/ | en_GB |
dc.relation.url | https://www.diabetesge nes.org/current-research/genetic-beta-cell-research-bank/ | en_GB |
dc.rights | © 2023. The Author(s). 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/. | en_GB |
dc.subject | Diabetes pregnancy | en_GB |
dc.subject | Glucokinase | en_GB |
dc.subject | MODY | en_GB |
dc.subject | Maturity-onset diabetes of the young | en_GB |
dc.subject | Non-invasive prenatal testing | en_GB |
dc.subject | Precision medicine | en_GB |
dc.subject | Ultrasound | en_GB |
dc.title | Bringing precision medicine to the management of pregnancy in women with glucokinase-MODY: a study of diagnostic accuracy and feasibility of non-invasive prenatal testing. | en_GB |
dc.type | Article | en_GB |
dc.date.available | 2023-09-15T09:08:22Z | |
dc.identifier.issn | 0012-186X | |
exeter.place-of-publication | Germany | |
dc.description | This is the final version. Available from Springer via the DOI in this record. | en_GB |
dc.description | Data availability Individual-level data used in this study are not freely available to protect the identity of research participants. Information for researchers and protocols for the study and submissions to the Genetic Beta Cell Research Bank are available online (https://www.diabetesge nes.org/current-research/gck-mody-nipt/ and https://www.diabetesge nes.org/current-research/genetic-beta-cell-research-bank/). Requests for additional data specifically related to this work are available to researchers through managed open collaboration. Requests will be considered after liaising with the relevant study and ethics committees, and should be made in writing to the corresponding author, AT Hattersley | en_GB |
dc.identifier.eissn | 1432-0428 | |
dc.identifier.journal | Diabetologia | en_GB |
dc.relation.ispartof | Diabetologia | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | en_GB |
dcterms.dateAccepted | 2023-06-08 | |
rioxxterms.version | VoR | en_GB |
rioxxterms.licenseref.startdate | 2023-08-31 | |
rioxxterms.type | Journal Article/Review | en_GB |
refterms.dateFCD | 2023-09-15T09:04:59Z | |
refterms.versionFCD | VoR | |
refterms.dateFOA | 2023-09-15T09:08:23Z | |
refterms.panel | A | en_GB |
refterms.dateFirstOnline | 2023-08-31 |
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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/.