HOMA‐IR as a risk factor of gestational diabetes mellitus and a novel simple surrogate index in early pregnancy
Objective To assess the association between insulin resistance and gestational diabetes mellitus (GDM) in early pregnancy and find a simple surrogate index of the homeostasis model assessment of insulin resistance (HOMA‐IR). Methods A total of 700 pregnant women were included in this prospective, do...
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Published in | International journal of gynecology and obstetrics Vol. 157; no. 3; pp. 694 - 701 |
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Main Authors | , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
01.06.2022
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Abstract | Objective
To assess the association between insulin resistance and gestational diabetes mellitus (GDM) in early pregnancy and find a simple surrogate index of the homeostasis model assessment of insulin resistance (HOMA‐IR).
Methods
A total of 700 pregnant women were included in this prospective, double‐center, observational cohort study. The glucose and lipid metabolic characterization was performed at 6–12 weeks of pregnancy. All participants underwent a 75‐g oral glucose tolerance test at 24–28 weeks of pregnancy. Linear regression analysis was applied to find a novel surrogate index of HOMA‐IR. Binary logistic analysis was applied to estimate possible associations of different indices with GDM and insulin resistance.
Results
GDM was diagnosed in 145 of 700 women with singleton pregnancies (20.7%). HOMA‐IR was higher in the GDM group than in the normal glucose tolerance (NGT) group and was an individual risk factor for GDM (adjusted risk ratio RR 1.371, 95% confidence interval [CI] 1.129–1.665, P < 0.001). TyHGB index as the surrogate index of HOMA‐IR was represented as TG/HDL‐C + 0.7*FBG (mmol/L) +0.1*preBMI (kg/m2)(where TG/HDL‐C is triglyceride/high‐density lipoprotein cholesterol; FBG is fasting blood glucose, and preBMI is the pre‐pregnancy body mass index [calculated as weight in kilograms divided by the square of height in meters]). The cut‐off point of the TyHGB index was 6.0 (area under the curve 0.827, 95% CI 0.794–0.861, P < 0.001) for mild insulin resistance.
Conclusion
Increased HOMA‐IR in early pregnancy was a risk factor of GDM. TyHGB index could be a surrogate index of HOMA‐IR and had a predictive value for GDM. |
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AbstractList | To assess the association between insulin resistance and gestational diabetes mellitus (GDM) in early pregnancy and find a simple surrogate index of the homeostasis model assessment of insulin resistance (HOMA-IR).
A total of 700 pregnant women were included in this prospective, double-center, observational cohort study. The glucose and lipid metabolic characterization was performed at 6-12 weeks of pregnancy. All participants underwent a 75-g oral glucose tolerance test at 24-28 weeks of pregnancy. Linear regression analysis was applied to find a novel surrogate index of HOMA-IR. Binary logistic analysis was applied to estimate possible associations of different indices with GDM and insulin resistance.
GDM was diagnosed in 145 of 700 women with singleton pregnancies (20.7%). HOMA-IR was higher in the GDM group than in the normal glucose tolerance (NGT) group and was an individual risk factor for GDM (adjusted risk ratio RR 1.371, 95% confidence interval [CI] 1.129-1.665, P < 0.001). TyHGB index as the surrogate index of HOMA-IR was represented as TG/HDL-C + 0.7*FBG (mmol/L) +0.1*preBMI (kg/m
)(where TG/HDL-C is triglyceride/high-density lipoprotein cholesterol; FBG is fasting blood glucose, and preBMI is the pre-pregnancy body mass index [calculated as weight in kilograms divided by the square of height in meters]). The cut-off point of the TyHGB index was 6.0 (area under the curve 0.827, 95% CI 0.794-0.861, P < 0.001) for mild insulin resistance.
Increased HOMA-IR in early pregnancy was a risk factor of GDM. TyHGB index could be a surrogate index of HOMA-IR and had a predictive value for GDM. Objective To assess the association between insulin resistance and gestational diabetes mellitus (GDM) in early pregnancy and find a simple surrogate index of the homeostasis model assessment of insulin resistance (HOMA‐IR). Methods A total of 700 pregnant women were included in this prospective, double‐center, observational cohort study. The glucose and lipid metabolic characterization was performed at 6–12 weeks of pregnancy. All participants underwent a 75‐g oral glucose tolerance test at 24–28 weeks of pregnancy. Linear regression analysis was applied to find a novel surrogate index of HOMA‐IR. Binary logistic analysis was applied to estimate possible associations of different indices with GDM and insulin resistance. Results GDM was diagnosed in 145 of 700 women with singleton pregnancies (20.7%). HOMA‐IR was higher in the GDM group than in the normal glucose tolerance (NGT) group and was an individual risk factor for GDM (adjusted risk ratio RR 1.371, 95% confidence interval [CI] 1.129–1.665, P < 0.001). TyHGB index as the surrogate index of HOMA‐IR was represented as TG/HDL‐C + 0.7*FBG (mmol/L) +0.1*preBMI (kg/m2)(where TG/HDL‐C is triglyceride/high‐density lipoprotein cholesterol; FBG is fasting blood glucose, and preBMI is the pre‐pregnancy body mass index [calculated as weight in kilograms divided by the square of height in meters]). The cut‐off point of the TyHGB index was 6.0 (area under the curve 0.827, 95% CI 0.794–0.861, P < 0.001) for mild insulin resistance. Conclusion Increased HOMA‐IR in early pregnancy was a risk factor of GDM. TyHGB index could be a surrogate index of HOMA‐IR and had a predictive value for GDM. To assess the association between insulin resistance and gestational diabetes mellitus (GDM) in early pregnancy and find a simple surrogate index of the homeostasis model assessment of insulin resistance (HOMA-IR).OBJECTIVETo assess the association between insulin resistance and gestational diabetes mellitus (GDM) in early pregnancy and find a simple surrogate index of the homeostasis model assessment of insulin resistance (HOMA-IR).A total of 700 pregnant women were included in this prospective, double-center, observational cohort study. The glucose and lipid metabolic characterization was performed at 6-12 weeks of pregnancy. All participants underwent a 75-g oral glucose tolerance test at 24-28 weeks of pregnancy. Linear regression analysis was applied to find a novel surrogate index of HOMA-IR. Binary logistic analysis was applied to estimate possible associations of different indices with GDM and insulin resistance.METHODSA total of 700 pregnant women were included in this prospective, double-center, observational cohort study. The glucose and lipid metabolic characterization was performed at 6-12 weeks of pregnancy. All participants underwent a 75-g oral glucose tolerance test at 24-28 weeks of pregnancy. Linear regression analysis was applied to find a novel surrogate index of HOMA-IR. Binary logistic analysis was applied to estimate possible associations of different indices with GDM and insulin resistance.GDM was diagnosed in 145 of 700 women with singleton pregnancies (20.7%). HOMA-IR was higher in the GDM group than in the normal glucose tolerance (NGT) group and was an individual risk factor for GDM (adjusted risk ratio RR 1.371, 95% confidence interval [CI] 1.129-1.665, P < 0.001). TyHGB index as the surrogate index of HOMA-IR was represented as TG/HDL-C + 0.7*FBG (mmol/L) +0.1*preBMI (kg/m2 )(where TG/HDL-C is triglyceride/high-density lipoprotein cholesterol; FBG is fasting blood glucose, and preBMI is the pre-pregnancy body mass index [calculated as weight in kilograms divided by the square of height in meters]). The cut-off point of the TyHGB index was 6.0 (area under the curve 0.827, 95% CI 0.794-0.861, P < 0.001) for mild insulin resistance.RESULTSGDM was diagnosed in 145 of 700 women with singleton pregnancies (20.7%). HOMA-IR was higher in the GDM group than in the normal glucose tolerance (NGT) group and was an individual risk factor for GDM (adjusted risk ratio RR 1.371, 95% confidence interval [CI] 1.129-1.665, P < 0.001). TyHGB index as the surrogate index of HOMA-IR was represented as TG/HDL-C + 0.7*FBG (mmol/L) +0.1*preBMI (kg/m2 )(where TG/HDL-C is triglyceride/high-density lipoprotein cholesterol; FBG is fasting blood glucose, and preBMI is the pre-pregnancy body mass index [calculated as weight in kilograms divided by the square of height in meters]). The cut-off point of the TyHGB index was 6.0 (area under the curve 0.827, 95% CI 0.794-0.861, P < 0.001) for mild insulin resistance.Increased HOMA-IR in early pregnancy was a risk factor of GDM. TyHGB index could be a surrogate index of HOMA-IR and had a predictive value for GDM.CONCLUSIONIncreased HOMA-IR in early pregnancy was a risk factor of GDM. TyHGB index could be a surrogate index of HOMA-IR and had a predictive value for GDM. |
Author | Peng, Zhenyao Sun, Qiujin Yuan, Tao Nie, Xiaorui Zhao, Tianyi Lu, Zechun Wang, Ailing Dong, Yingyue Chen, Yan Zhao, Weigang Qiao, Xiaolin Yang, Xianchun Sun, Wei Zhang, Jing Song, Shuoning Liu, Shixuan Duo, Yanbei Xu, Jiyu Zhang, Yuemei Fu, Yong |
Author_xml | – sequence: 1 givenname: Shuoning surname: Song fullname: Song, Shuoning organization: Chinese Academy of Medical Science and Peking Union Medical College – sequence: 2 givenname: Yuemei surname: Zhang fullname: Zhang, Yuemei organization: Haidian District Maternal and Child Health Care Hospital – sequence: 3 givenname: Xiaolin surname: Qiao fullname: Qiao, Xiaolin organization: Beijing Chaoyang District Maternal and Child Health Care Hospital – sequence: 4 givenname: Yanbei surname: Duo fullname: Duo, Yanbei organization: Chinese Academy of Medical Science and Peking Union Medical College – sequence: 5 givenname: Jiyu surname: Xu fullname: Xu, Jiyu organization: Peking Union Medical College – sequence: 6 givenname: Zhenyao surname: Peng fullname: Peng, Zhenyao organization: Haidian District Maternal and Child Health Care Hospital – sequence: 7 givenname: Jing surname: Zhang fullname: Zhang, Jing organization: Haidian District Maternal and Child Health Care Hospital – sequence: 8 givenname: Yan surname: Chen fullname: Chen, Yan organization: Beijing Chaoyang District Maternal and Child Health Care Hospital – sequence: 9 givenname: Xiaorui surname: Nie fullname: Nie, Xiaorui organization: Beijing Chaoyang District Maternal and Child Health Care Hospital – sequence: 10 givenname: Qiujin surname: Sun fullname: Sun, Qiujin organization: Beijing Chaoyang District Maternal and Child Health Care Hospital – sequence: 11 givenname: Xianchun surname: Yang fullname: Yang, Xianchun organization: Beijing Chaoyang District Maternal and Child Health Care Hospital – sequence: 12 givenname: Zechun surname: Lu fullname: Lu, Zechun organization: China CDC – sequence: 13 givenname: Shixuan surname: Liu fullname: Liu, Shixuan organization: Chinese Academy of Medical Science and Peking Union Medical College – sequence: 14 givenname: Tianyi surname: Zhao fullname: Zhao, Tianyi organization: Chinese Academy of Medical Science and Peking Union Medical College – sequence: 15 givenname: Tao surname: Yuan fullname: Yuan, Tao organization: Chinese Academy of Medical Science and Peking Union Medical College – sequence: 16 givenname: Yong surname: Fu fullname: Fu, Yong organization: Chinese Academy of Medical Science and Peking Union Medical College – sequence: 17 givenname: Yingyue surname: Dong fullname: Dong, Yingyue organization: Chinese Academy of Medical Science and Peking Union Medical College – sequence: 18 givenname: Weigang orcidid: 0000-0002-1472-7118 surname: Zhao fullname: Zhao, Weigang email: xiehezhaoweigang@163.com organization: Chinese Academy of Medical Science and Peking Union Medical College – sequence: 19 givenname: Wei surname: Sun fullname: Sun, Wei organization: Peking Union Medical College – sequence: 20 givenname: Ailing surname: Wang fullname: Wang, Ailing organization: China CDC |
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Notes | Funding information Shuoning Song, Yuemei Zhang, and Xiaolin Qiao contributed equally to this article. This study was supported by 13th Five‐Year National Science and Technology Major Project for New Drugs under Grant No. 2019ZX09734001 (to WZ). ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Undefined-3 |
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Snippet | Objective
To assess the association between insulin resistance and gestational diabetes mellitus (GDM) in early pregnancy and find a simple surrogate index of... To assess the association between insulin resistance and gestational diabetes mellitus (GDM) in early pregnancy and find a simple surrogate index of the... |
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StartPage | 694 |
SubjectTerms | gestational diabetes mellitus glucose and lipid metabolism HOMA‐IR insulin resistance |
Title | HOMA‐IR as a risk factor of gestational diabetes mellitus and a novel simple surrogate index in early pregnancy |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fijgo.13905 https://www.ncbi.nlm.nih.gov/pubmed/34449903 https://www.proquest.com/docview/2566040619 |
Volume | 157 |
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