Predictors of later insulin therapy for gestational diabetes diagnosed in early pregnancy

Interventions for gestational diabetes mellitus (GDM), diagnosed in early pregnancy, have been a topic of controversy. This study aimed to elucidate factors that predict patients with GDM diagnosed before 24 gestational weeks (early GDM: E-GDM) who require insulin therapy later during pregnancy. Fur...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:ENDOCRINE JOURNAL 2021, Vol.68(11), pp.1321-1328
Hauptverfasser: Tamagawa, Masumi, Kasuga, Yoshifumi, Saisho, Yoshifumi, Tanaka, Yuya, Hasegawa, Keita, Oishi, Maki, Endo, Toyohide, Sato, Yu, Ikenoue, Satoru, Tanaka, Mamoru, Ochiai, Daigo
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1328
container_issue 11
container_start_page 1321
container_title ENDOCRINE JOURNAL
container_volume 68
creator Tamagawa, Masumi
Kasuga, Yoshifumi
Saisho, Yoshifumi
Tanaka, Yuya
Hasegawa, Keita
Oishi, Maki
Endo, Toyohide
Sato, Yu
Ikenoue, Satoru
Tanaka, Mamoru
Ochiai, Daigo
description Interventions for gestational diabetes mellitus (GDM), diagnosed in early pregnancy, have been a topic of controversy. This study aimed to elucidate factors that predict patients with GDM diagnosed before 24 gestational weeks (early GDM: E-GDM) who require insulin therapy later during pregnancy. Furthermore, we identified patients whose impaired glucose tolerance should be strictly controlled from early gestation onward. Women diagnosed with GDM were categorized based on the gestational age at diagnosis into E-GDM (n = 388) or late GDM (L-GDM, diagnosed after 24 weeks, n = 340) groups. Clinical features were compared between the groups, and the predictors for insulin therapy was evaluated in the E-GDM group. There were no significant between-group differences in terms of perinatal outcomes (e.g., gestational weeks at delivery, fetal growth, hypertensive disorder of pregnancy), with the exception of the Apgar score at 5 min. Moreover, there was no significant difference in the frequency of insulin therapy during pregnancy between the two groups. Using multiple logistic regression analysis, pre-pregnancy body mass index (BMI) ≥25 kg/m2, a family history of diabetes, and higher fasting plasma glucose (FPG), 1 h-plasma glucose (PG), and 2 h-PG values increased insulin therapy risk during pregnancy in the E-GDM group. Furthermore, since E-GDM patients with abnormal levels of FPG, as well as 1 h-PG or 2 h-PG, and those with pre-pregnancy BMI ≥25 kg/m2 and a family history of diabetes had a higher risk of later insulin therapy during pregnancy, they may require more careful follow-up in the perinatal period.
doi_str_mv 10.1507/endocrj.EJ21-0118
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2605319901</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2605319901</sourcerecordid><originalsourceid>FETCH-LOGICAL-c659t-daceed67c4435b0f161117070fd6b6f404a4800a8b57c5c86549cd8fb176c9513</originalsourceid><addsrcrecordid>eNpFkE9vEzEQxS0EoqHwAbggS5y3zMR_1j6iqrSgSnCgh54sr-1NN9qsU3tzyLfHbtLlMmNL7715-hHyGeEKBbTfwuSjS9urm19rbABRvSErZFw1XHB4S1agUTVKC31BPuS8BWBMcPaeXDCOoBjCijz-ScEPbo4p09jT0c4h0WHKh3GY6PwUkt0faR8T3YQ823mIkx2pH2wX5pDrYzPFHHyx0GDTeKT7FDaTndzxI3nX2zGHT-d9SR5-3Py9vmvuf9_-vP5-3zgp9Nx460LwsnWcM9FBjxIRW2ih97KTPQduuQKwqhOtE05JwbXzqu-wlU4LZJfk6yl3n-LzobQ023hIpWY2awmCodZQVXhSuRRzTqE3-zTsbDoaBFNhmjNMU2GaCrN4vpyTD90u-MXxSq8Ibk-CXWVoxzgVauH_ffcsX1LNGmomSIV1tQZZ-ZehmF4jg5p0d0raFsqbsJyyaR7cGJZyUpkSUebScpG4J5uKjv0D2_eiag</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2605319901</pqid></control><display><type>article</type><title>Predictors of later insulin therapy for gestational diabetes diagnosed in early pregnancy</title><source>MEDLINE</source><source>J-STAGE (Japan Science &amp; Technology Information Aggregator, Electronic) Freely Available Titles - Japanese</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Tamagawa, Masumi ; Kasuga, Yoshifumi ; Saisho, Yoshifumi ; Tanaka, Yuya ; Hasegawa, Keita ; Oishi, Maki ; Endo, Toyohide ; Sato, Yu ; Ikenoue, Satoru ; Tanaka, Mamoru ; Ochiai, Daigo</creator><creatorcontrib>Tamagawa, Masumi ; Kasuga, Yoshifumi ; Saisho, Yoshifumi ; Tanaka, Yuya ; Hasegawa, Keita ; Oishi, Maki ; Endo, Toyohide ; Sato, Yu ; Ikenoue, Satoru ; Tanaka, Mamoru ; Ochiai, Daigo ; Department of Obstetrics and Gynecology ; Keio University School of Medicine ; Department of Internal Medicine</creatorcontrib><description>Interventions for gestational diabetes mellitus (GDM), diagnosed in early pregnancy, have been a topic of controversy. This study aimed to elucidate factors that predict patients with GDM diagnosed before 24 gestational weeks (early GDM: E-GDM) who require insulin therapy later during pregnancy. Furthermore, we identified patients whose impaired glucose tolerance should be strictly controlled from early gestation onward. Women diagnosed with GDM were categorized based on the gestational age at diagnosis into E-GDM (n = 388) or late GDM (L-GDM, diagnosed after 24 weeks, n = 340) groups. Clinical features were compared between the groups, and the predictors for insulin therapy was evaluated in the E-GDM group. There were no significant between-group differences in terms of perinatal outcomes (e.g., gestational weeks at delivery, fetal growth, hypertensive disorder of pregnancy), with the exception of the Apgar score at 5 min. Moreover, there was no significant difference in the frequency of insulin therapy during pregnancy between the two groups. Using multiple logistic regression analysis, pre-pregnancy body mass index (BMI) ≥25 kg/m2, a family history of diabetes, and higher fasting plasma glucose (FPG), 1 h-plasma glucose (PG), and 2 h-PG values increased insulin therapy risk during pregnancy in the E-GDM group. Furthermore, since E-GDM patients with abnormal levels of FPG, as well as 1 h-PG or 2 h-PG, and those with pre-pregnancy BMI ≥25 kg/m2 and a family history of diabetes had a higher risk of later insulin therapy during pregnancy, they may require more careful follow-up in the perinatal period.</description><identifier>ISSN: 0918-8959</identifier><identifier>EISSN: 1348-4540</identifier><identifier>DOI: 10.1507/endocrj.EJ21-0118</identifier><identifier>PMID: 34108310</identifier><language>eng</language><publisher>Japan: The Japan Endocrine Society</publisher><subject>Adult ; Apgar score ; Blood Glucose ; Body Mass Index ; Diabetes mellitus ; Diabetes, Gestational - blood ; Diabetes, Gestational - diagnosis ; Diabetes, Gestational - drug therapy ; Female ; Fetuses ; Gestational age ; Gestational diabetes ; Glucose ; Glucose Intolerance ; Glucose tolerance ; Glucose Tolerance Test ; Humans ; Hypoglycemic Agents - therapeutic use ; Insulin ; Insulin - blood ; Insulin - therapeutic use ; Obesity ; Oral glucose tolerance test ; Patients ; Pregnancy ; Risk Factors</subject><ispartof>Endocrine Journal, 2021, Vol.68(11), pp.1321-1328</ispartof><rights>The Japan Endocrine Society</rights><rights>Copyright Japan Science and Technology Agency 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c659t-daceed67c4435b0f161117070fd6b6f404a4800a8b57c5c86549cd8fb176c9513</citedby><cites>FETCH-LOGICAL-c659t-daceed67c4435b0f161117070fd6b6f404a4800a8b57c5c86549cd8fb176c9513</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34108310$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tamagawa, Masumi</creatorcontrib><creatorcontrib>Kasuga, Yoshifumi</creatorcontrib><creatorcontrib>Saisho, Yoshifumi</creatorcontrib><creatorcontrib>Tanaka, Yuya</creatorcontrib><creatorcontrib>Hasegawa, Keita</creatorcontrib><creatorcontrib>Oishi, Maki</creatorcontrib><creatorcontrib>Endo, Toyohide</creatorcontrib><creatorcontrib>Sato, Yu</creatorcontrib><creatorcontrib>Ikenoue, Satoru</creatorcontrib><creatorcontrib>Tanaka, Mamoru</creatorcontrib><creatorcontrib>Ochiai, Daigo</creatorcontrib><creatorcontrib>Department of Obstetrics and Gynecology</creatorcontrib><creatorcontrib>Keio University School of Medicine</creatorcontrib><creatorcontrib>Department of Internal Medicine</creatorcontrib><title>Predictors of later insulin therapy for gestational diabetes diagnosed in early pregnancy</title><title>ENDOCRINE JOURNAL</title><addtitle>Endocr J</addtitle><description>Interventions for gestational diabetes mellitus (GDM), diagnosed in early pregnancy, have been a topic of controversy. This study aimed to elucidate factors that predict patients with GDM diagnosed before 24 gestational weeks (early GDM: E-GDM) who require insulin therapy later during pregnancy. Furthermore, we identified patients whose impaired glucose tolerance should be strictly controlled from early gestation onward. Women diagnosed with GDM were categorized based on the gestational age at diagnosis into E-GDM (n = 388) or late GDM (L-GDM, diagnosed after 24 weeks, n = 340) groups. Clinical features were compared between the groups, and the predictors for insulin therapy was evaluated in the E-GDM group. There were no significant between-group differences in terms of perinatal outcomes (e.g., gestational weeks at delivery, fetal growth, hypertensive disorder of pregnancy), with the exception of the Apgar score at 5 min. Moreover, there was no significant difference in the frequency of insulin therapy during pregnancy between the two groups. Using multiple logistic regression analysis, pre-pregnancy body mass index (BMI) ≥25 kg/m2, a family history of diabetes, and higher fasting plasma glucose (FPG), 1 h-plasma glucose (PG), and 2 h-PG values increased insulin therapy risk during pregnancy in the E-GDM group. Furthermore, since E-GDM patients with abnormal levels of FPG, as well as 1 h-PG or 2 h-PG, and those with pre-pregnancy BMI ≥25 kg/m2 and a family history of diabetes had a higher risk of later insulin therapy during pregnancy, they may require more careful follow-up in the perinatal period.</description><subject>Adult</subject><subject>Apgar score</subject><subject>Blood Glucose</subject><subject>Body Mass Index</subject><subject>Diabetes mellitus</subject><subject>Diabetes, Gestational - blood</subject><subject>Diabetes, Gestational - diagnosis</subject><subject>Diabetes, Gestational - drug therapy</subject><subject>Female</subject><subject>Fetuses</subject><subject>Gestational age</subject><subject>Gestational diabetes</subject><subject>Glucose</subject><subject>Glucose Intolerance</subject><subject>Glucose tolerance</subject><subject>Glucose Tolerance Test</subject><subject>Humans</subject><subject>Hypoglycemic Agents - therapeutic use</subject><subject>Insulin</subject><subject>Insulin - blood</subject><subject>Insulin - therapeutic use</subject><subject>Obesity</subject><subject>Oral glucose tolerance test</subject><subject>Patients</subject><subject>Pregnancy</subject><subject>Risk Factors</subject><issn>0918-8959</issn><issn>1348-4540</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE9vEzEQxS0EoqHwAbggS5y3zMR_1j6iqrSgSnCgh54sr-1NN9qsU3tzyLfHbtLlMmNL7715-hHyGeEKBbTfwuSjS9urm19rbABRvSErZFw1XHB4S1agUTVKC31BPuS8BWBMcPaeXDCOoBjCijz-ScEPbo4p09jT0c4h0WHKh3GY6PwUkt0faR8T3YQ823mIkx2pH2wX5pDrYzPFHHyx0GDTeKT7FDaTndzxI3nX2zGHT-d9SR5-3Py9vmvuf9_-vP5-3zgp9Nx460LwsnWcM9FBjxIRW2ih97KTPQduuQKwqhOtE05JwbXzqu-wlU4LZJfk6yl3n-LzobQ023hIpWY2awmCodZQVXhSuRRzTqE3-zTsbDoaBFNhmjNMU2GaCrN4vpyTD90u-MXxSq8Ibk-CXWVoxzgVauH_ffcsX1LNGmomSIV1tQZZ-ZehmF4jg5p0d0raFsqbsJyyaR7cGJZyUpkSUebScpG4J5uKjv0D2_eiag</recordid><startdate>20210101</startdate><enddate>20210101</enddate><creator>Tamagawa, Masumi</creator><creator>Kasuga, Yoshifumi</creator><creator>Saisho, Yoshifumi</creator><creator>Tanaka, Yuya</creator><creator>Hasegawa, Keita</creator><creator>Oishi, Maki</creator><creator>Endo, Toyohide</creator><creator>Sato, Yu</creator><creator>Ikenoue, Satoru</creator><creator>Tanaka, Mamoru</creator><creator>Ochiai, Daigo</creator><general>The Japan Endocrine Society</general><general>Japan Science and Technology Agency</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7T5</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20210101</creationdate><title>Predictors of later insulin therapy for gestational diabetes diagnosed in early pregnancy</title><author>Tamagawa, Masumi ; Kasuga, Yoshifumi ; Saisho, Yoshifumi ; Tanaka, Yuya ; Hasegawa, Keita ; Oishi, Maki ; Endo, Toyohide ; Sato, Yu ; Ikenoue, Satoru ; Tanaka, Mamoru ; Ochiai, Daigo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c659t-daceed67c4435b0f161117070fd6b6f404a4800a8b57c5c86549cd8fb176c9513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adult</topic><topic>Apgar score</topic><topic>Blood Glucose</topic><topic>Body Mass Index</topic><topic>Diabetes mellitus</topic><topic>Diabetes, Gestational - blood</topic><topic>Diabetes, Gestational - diagnosis</topic><topic>Diabetes, Gestational - drug therapy</topic><topic>Female</topic><topic>Fetuses</topic><topic>Gestational age</topic><topic>Gestational diabetes</topic><topic>Glucose</topic><topic>Glucose Intolerance</topic><topic>Glucose tolerance</topic><topic>Glucose Tolerance Test</topic><topic>Humans</topic><topic>Hypoglycemic Agents - therapeutic use</topic><topic>Insulin</topic><topic>Insulin - blood</topic><topic>Insulin - therapeutic use</topic><topic>Obesity</topic><topic>Oral glucose tolerance test</topic><topic>Patients</topic><topic>Pregnancy</topic><topic>Risk Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tamagawa, Masumi</creatorcontrib><creatorcontrib>Kasuga, Yoshifumi</creatorcontrib><creatorcontrib>Saisho, Yoshifumi</creatorcontrib><creatorcontrib>Tanaka, Yuya</creatorcontrib><creatorcontrib>Hasegawa, Keita</creatorcontrib><creatorcontrib>Oishi, Maki</creatorcontrib><creatorcontrib>Endo, Toyohide</creatorcontrib><creatorcontrib>Sato, Yu</creatorcontrib><creatorcontrib>Ikenoue, Satoru</creatorcontrib><creatorcontrib>Tanaka, Mamoru</creatorcontrib><creatorcontrib>Ochiai, Daigo</creatorcontrib><creatorcontrib>Department of Obstetrics and Gynecology</creatorcontrib><creatorcontrib>Keio University School of Medicine</creatorcontrib><creatorcontrib>Department of Internal Medicine</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>ENDOCRINE JOURNAL</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tamagawa, Masumi</au><au>Kasuga, Yoshifumi</au><au>Saisho, Yoshifumi</au><au>Tanaka, Yuya</au><au>Hasegawa, Keita</au><au>Oishi, Maki</au><au>Endo, Toyohide</au><au>Sato, Yu</au><au>Ikenoue, Satoru</au><au>Tanaka, Mamoru</au><au>Ochiai, Daigo</au><aucorp>Department of Obstetrics and Gynecology</aucorp><aucorp>Keio University School of Medicine</aucorp><aucorp>Department of Internal Medicine</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Predictors of later insulin therapy for gestational diabetes diagnosed in early pregnancy</atitle><jtitle>ENDOCRINE JOURNAL</jtitle><addtitle>Endocr J</addtitle><date>2021-01-01</date><risdate>2021</risdate><volume>68</volume><issue>11</issue><spage>1321</spage><epage>1328</epage><pages>1321-1328</pages><artnum>EJ21-0118</artnum><issn>0918-8959</issn><eissn>1348-4540</eissn><abstract>Interventions for gestational diabetes mellitus (GDM), diagnosed in early pregnancy, have been a topic of controversy. This study aimed to elucidate factors that predict patients with GDM diagnosed before 24 gestational weeks (early GDM: E-GDM) who require insulin therapy later during pregnancy. Furthermore, we identified patients whose impaired glucose tolerance should be strictly controlled from early gestation onward. Women diagnosed with GDM were categorized based on the gestational age at diagnosis into E-GDM (n = 388) or late GDM (L-GDM, diagnosed after 24 weeks, n = 340) groups. Clinical features were compared between the groups, and the predictors for insulin therapy was evaluated in the E-GDM group. There were no significant between-group differences in terms of perinatal outcomes (e.g., gestational weeks at delivery, fetal growth, hypertensive disorder of pregnancy), with the exception of the Apgar score at 5 min. Moreover, there was no significant difference in the frequency of insulin therapy during pregnancy between the two groups. Using multiple logistic regression analysis, pre-pregnancy body mass index (BMI) ≥25 kg/m2, a family history of diabetes, and higher fasting plasma glucose (FPG), 1 h-plasma glucose (PG), and 2 h-PG values increased insulin therapy risk during pregnancy in the E-GDM group. Furthermore, since E-GDM patients with abnormal levels of FPG, as well as 1 h-PG or 2 h-PG, and those with pre-pregnancy BMI ≥25 kg/m2 and a family history of diabetes had a higher risk of later insulin therapy during pregnancy, they may require more careful follow-up in the perinatal period.</abstract><cop>Japan</cop><pub>The Japan Endocrine Society</pub><pmid>34108310</pmid><doi>10.1507/endocrj.EJ21-0118</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0918-8959
ispartof Endocrine Journal, 2021, Vol.68(11), pp.1321-1328
issn 0918-8959
1348-4540
language eng
recordid cdi_proquest_journals_2605319901
source MEDLINE; J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - Japanese; EZB-FREE-00999 freely available EZB journals
subjects Adult
Apgar score
Blood Glucose
Body Mass Index
Diabetes mellitus
Diabetes, Gestational - blood
Diabetes, Gestational - diagnosis
Diabetes, Gestational - drug therapy
Female
Fetuses
Gestational age
Gestational diabetes
Glucose
Glucose Intolerance
Glucose tolerance
Glucose Tolerance Test
Humans
Hypoglycemic Agents - therapeutic use
Insulin
Insulin - blood
Insulin - therapeutic use
Obesity
Oral glucose tolerance test
Patients
Pregnancy
Risk Factors
title Predictors of later insulin therapy for gestational diabetes diagnosed in early pregnancy
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-14T09%3A17%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Predictors%20of%20later%20insulin%20therapy%20for%20gestational%20diabetes%20diagnosed%20in%20early%20pregnancy&rft.jtitle=ENDOCRINE%20JOURNAL&rft.au=Tamagawa,%20Masumi&rft.aucorp=Department%20of%20Obstetrics%20and%20Gynecology&rft.date=2021-01-01&rft.volume=68&rft.issue=11&rft.spage=1321&rft.epage=1328&rft.pages=1321-1328&rft.artnum=EJ21-0118&rft.issn=0918-8959&rft.eissn=1348-4540&rft_id=info:doi/10.1507/endocrj.EJ21-0118&rft_dat=%3Cproquest_cross%3E2605319901%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2605319901&rft_id=info:pmid/34108310&rfr_iscdi=true