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Prospective Evaluation of Fetal Hemoglobin Expression in Maternal Erythrocytes: An Analysis of a Cohort of 345 Parturients
It is believed that fetal hemoglobin (HbF) expression in adults is largely genetically regulated. The increased expression of HbF in pregnancy has been reported in a small number of articles. Different mechanisms have been proposed, but the description of HbF expression during pregnancy remains uncl...
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Published in: | Diagnostics (Basel) 2023-05, Vol.13 (11), p.1873 |
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creator | Blain, Laurence Watier, Christian Weng, Xiaoduan Masse, Andre Bédard, Marie-Josée Bettache, Nazila Weber, Florence Mahone, Michele Forté, Stéphanie Lavallée, Vincent-Philippe Gaudreau, Pierre-Olivier Newmarch, Michael J Soulières, Denis |
description | It is believed that fetal hemoglobin (HbF) expression in adults is largely genetically regulated. The increased expression of HbF in pregnancy has been reported in a small number of articles. Different mechanisms have been proposed, but the description of HbF expression during pregnancy remains unclear. The objectives of this study were to document HbF expression during peri and postpartum periods, confirm its maternal origin, and assess clinical and biochemical parameters potentially associated with HbF modulation. In this observational prospective study, 345 pregnant women were followed. At baseline, 169 had HbF expression (≥1% of total hemoglobin) and 176 did not have HbF expression. Women were followed at the obstetric clinic during their pregnancy. Clinical and biochemical parameters were measured at each visit. Analyses were made to determine which parameters had a significant correlation to HbF expression. Results show that HbF expression of ≥1% during peri and postpartum periods in pregnant women without influencing comorbidities is at its highest peak during the first trimester. In all women, it was proven that HbF was of maternal origin. A significant positive correlation between HbF expression, βeta-human chorionic gonadotropin (β-HCG), and glycosylated hemoglobin (HbA1c) was present. A significant negative association between HbF expression and total hemoglobin was found. HbF expression induction during pregnancy is probably associated with an increase in β-HCG and HbA1C, and a decrease in total hemoglobin, which could temporarily reactivate the fetal erythropoietic system. |
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The increased expression of HbF in pregnancy has been reported in a small number of articles. Different mechanisms have been proposed, but the description of HbF expression during pregnancy remains unclear. The objectives of this study were to document HbF expression during peri and postpartum periods, confirm its maternal origin, and assess clinical and biochemical parameters potentially associated with HbF modulation. In this observational prospective study, 345 pregnant women were followed. At baseline, 169 had HbF expression (≥1% of total hemoglobin) and 176 did not have HbF expression. Women were followed at the obstetric clinic during their pregnancy. Clinical and biochemical parameters were measured at each visit. Analyses were made to determine which parameters had a significant correlation to HbF expression. Results show that HbF expression of ≥1% during peri and postpartum periods in pregnant women without influencing comorbidities is at its highest peak during the first trimester. In all women, it was proven that HbF was of maternal origin. A significant positive correlation between HbF expression, βeta-human chorionic gonadotropin (β-HCG), and glycosylated hemoglobin (HbA1c) was present. A significant negative association between HbF expression and total hemoglobin was found. HbF expression induction during pregnancy is probably associated with an increase in β-HCG and HbA1C, and a decrease in total hemoglobin, which could temporarily reactivate the fetal erythropoietic system.</description><identifier>ISSN: 2075-4418</identifier><identifier>EISSN: 2075-4418</identifier><identifier>DOI: 10.3390/diagnostics13111873</identifier><identifier>PMID: 37296725</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Adults ; Analysis ; Blood diseases ; Chorionic gonadotropin ; Creatinine ; Diabetes ; Eclampsia ; fetal hemoglobin ; Glucose ; Glycoproteins ; Glycosylated hemoglobin ; HbA1C ; Hemoglobin ; Hypertension ; Laboratories ; Menstruation ; Obstetrics ; Preeclampsia ; Pregnancy ; Pregnant women ; Ultrasonic imaging ; Womens health ; β-HCG</subject><ispartof>Diagnostics (Basel), 2023-05, Vol.13 (11), p.1873</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c517t-8740041918fb9bfc93f3584614d040c75733b1507f774c31291c05295e89625c3</cites><orcidid>0000-0002-2269-212X ; 0000-0002-1533-3815 ; 0000-0003-2434-9234 ; 0000-0001-9095-0066</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2823979415/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2823979415?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792,74997</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37296725$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Blain, Laurence</creatorcontrib><creatorcontrib>Watier, Christian</creatorcontrib><creatorcontrib>Weng, Xiaoduan</creatorcontrib><creatorcontrib>Masse, Andre</creatorcontrib><creatorcontrib>Bédard, Marie-Josée</creatorcontrib><creatorcontrib>Bettache, Nazila</creatorcontrib><creatorcontrib>Weber, Florence</creatorcontrib><creatorcontrib>Mahone, Michele</creatorcontrib><creatorcontrib>Forté, Stéphanie</creatorcontrib><creatorcontrib>Lavallée, Vincent-Philippe</creatorcontrib><creatorcontrib>Gaudreau, Pierre-Olivier</creatorcontrib><creatorcontrib>Newmarch, Michael J</creatorcontrib><creatorcontrib>Soulières, Denis</creatorcontrib><title>Prospective Evaluation of Fetal Hemoglobin Expression in Maternal Erythrocytes: An Analysis of a Cohort of 345 Parturients</title><title>Diagnostics (Basel)</title><addtitle>Diagnostics (Basel)</addtitle><description>It is believed that fetal hemoglobin (HbF) expression in adults is largely genetically regulated. The increased expression of HbF in pregnancy has been reported in a small number of articles. Different mechanisms have been proposed, but the description of HbF expression during pregnancy remains unclear. The objectives of this study were to document HbF expression during peri and postpartum periods, confirm its maternal origin, and assess clinical and biochemical parameters potentially associated with HbF modulation. In this observational prospective study, 345 pregnant women were followed. At baseline, 169 had HbF expression (≥1% of total hemoglobin) and 176 did not have HbF expression. Women were followed at the obstetric clinic during their pregnancy. Clinical and biochemical parameters were measured at each visit. Analyses were made to determine which parameters had a significant correlation to HbF expression. Results show that HbF expression of ≥1% during peri and postpartum periods in pregnant women without influencing comorbidities is at its highest peak during the first trimester. In all women, it was proven that HbF was of maternal origin. A significant positive correlation between HbF expression, βeta-human chorionic gonadotropin (β-HCG), and glycosylated hemoglobin (HbA1c) was present. A significant negative association between HbF expression and total hemoglobin was found. HbF expression induction during pregnancy is probably associated with an increase in β-HCG and HbA1C, and a decrease in total hemoglobin, which could temporarily reactivate the fetal erythropoietic system.</description><subject>Adults</subject><subject>Analysis</subject><subject>Blood diseases</subject><subject>Chorionic gonadotropin</subject><subject>Creatinine</subject><subject>Diabetes</subject><subject>Eclampsia</subject><subject>fetal hemoglobin</subject><subject>Glucose</subject><subject>Glycoproteins</subject><subject>Glycosylated hemoglobin</subject><subject>HbA1C</subject><subject>Hemoglobin</subject><subject>Hypertension</subject><subject>Laboratories</subject><subject>Menstruation</subject><subject>Obstetrics</subject><subject>Preeclampsia</subject><subject>Pregnancy</subject><subject>Pregnant women</subject><subject>Ultrasonic imaging</subject><subject>Womens health</subject><subject>β-HCG</subject><issn>2075-4418</issn><issn>2075-4418</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUk1vEzEQXSEQrUp_ARJaiQuXtB5_rG0uKIpSWqmIHuBseb3ejaPNOtjeiPDr8TZtaVBtSx7PvPfGM5qieA_oghCJLhunu8HH5EwEAgCCk1fFKUaczSgF8fqZfVKcx7hGeUkgArO3xQnhWFYcs9Piz13wcWtNcjtbLne6H3Vyfih9W17ZpPvy2m581_vaDeXy9zbYGKdwfn3TyYYhI5Zhn1bBm32y8XM5H_LR_T66OInocuFXPqTJJpSVdzqkMTg7pPiueNPqPtrzh_us-Hm1_LG4nt1-_3qzmN_ODAOeZoJThChIEG0t69ZI0hImaAW0QRQZzjghNTDEW86pIYAlGMSwZFbICjNDzoqbg27j9Vptg9vosFdeO3Xv8KFT-VPO9FYhU1OMKuA0ZwVqamFaAQ0YoomWVmatLwet7VhvbGNyHUH3R6LHkcGtVOd3ChBmmEqaFT49KAT_a7QxqY2Lxva9Hqwfo8IC00pwVlUZ-vE_6NqPU8vvUURySYH9Q3U6V-CG1ufEZhJVc55zckqlyKiLF1B5N3bjjB9s67L_iEAOBJMHJAbbPhUJSE0jqF4Ywcz68Lw_T5zHgSN_Acg316s</recordid><startdate>20230527</startdate><enddate>20230527</enddate><creator>Blain, Laurence</creator><creator>Watier, Christian</creator><creator>Weng, Xiaoduan</creator><creator>Masse, Andre</creator><creator>Bédard, Marie-Josée</creator><creator>Bettache, Nazila</creator><creator>Weber, Florence</creator><creator>Mahone, Michele</creator><creator>Forté, Stéphanie</creator><creator>Lavallée, Vincent-Philippe</creator><creator>Gaudreau, Pierre-Olivier</creator><creator>Newmarch, Michael J</creator><creator>Soulières, Denis</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-2269-212X</orcidid><orcidid>https://orcid.org/0000-0002-1533-3815</orcidid><orcidid>https://orcid.org/0000-0003-2434-9234</orcidid><orcidid>https://orcid.org/0000-0001-9095-0066</orcidid></search><sort><creationdate>20230527</creationdate><title>Prospective Evaluation of Fetal Hemoglobin Expression in Maternal Erythrocytes: An Analysis of a Cohort of 345 Parturients</title><author>Blain, Laurence ; 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The increased expression of HbF in pregnancy has been reported in a small number of articles. Different mechanisms have been proposed, but the description of HbF expression during pregnancy remains unclear. The objectives of this study were to document HbF expression during peri and postpartum periods, confirm its maternal origin, and assess clinical and biochemical parameters potentially associated with HbF modulation. In this observational prospective study, 345 pregnant women were followed. At baseline, 169 had HbF expression (≥1% of total hemoglobin) and 176 did not have HbF expression. Women were followed at the obstetric clinic during their pregnancy. Clinical and biochemical parameters were measured at each visit. Analyses were made to determine which parameters had a significant correlation to HbF expression. Results show that HbF expression of ≥1% during peri and postpartum periods in pregnant women without influencing comorbidities is at its highest peak during the first trimester. In all women, it was proven that HbF was of maternal origin. A significant positive correlation between HbF expression, βeta-human chorionic gonadotropin (β-HCG), and glycosylated hemoglobin (HbA1c) was present. A significant negative association between HbF expression and total hemoglobin was found. 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subjects | Adults Analysis Blood diseases Chorionic gonadotropin Creatinine Diabetes Eclampsia fetal hemoglobin Glucose Glycoproteins Glycosylated hemoglobin HbA1C Hemoglobin Hypertension Laboratories Menstruation Obstetrics Preeclampsia Pregnancy Pregnant women Ultrasonic imaging Womens health β-HCG |
title | Prospective Evaluation of Fetal Hemoglobin Expression in Maternal Erythrocytes: An Analysis of a Cohort of 345 Parturients |
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