Search citation statements
Paper Sections
Citation Types
Year Published
Publication Types
Relationship
Authors
Journals
Background. The relationship among elevated serum β-human chorionic gonadotropin (β-hCG), the incidence of pregnancy complications, and adverse pregnancy outcomes has been controversial. Differences in study design, subject bias due to demographic characteristics, and differences in local medical levels could contribute to inconsistent results. Methods. Literature searches were performed in PubMed, EMBASE, Medline, Central, China National Knowledge Infrastructure (CNKI), Wanfang, and China Science Digital Library (CSDL) databases. Inclusion criteria were as follows: (1) research subjects were singleton pregnant women; (2) the study is identified as cohort study; (3) the subjects were assigned to the high β-hCG group and control group according to whether the exposure factors increased β-hCG in the second trimester; (4) the observed outcomes include at least pregnancy-induced hypertension (PIH), diabetes (gestational diabetes mellitus, GMD), preterm delivery (PD), and intrauterine growth restriction (IUGR); and (5) the odds ratio (OR) and 95% confidence interval (CI) of exposure factors are calculated based on literature dataset. To determine the risk bias of selected literatures, Newcastle-Ottawa scale was applied. The chi-square test was further used for heterogeneity analysis. If heterogeneity was identified, subgroup analyses were then performed for source investigation. Results. A total of 13 literatures were included and analyzed, including 67,355 pregnant women and 5980 pregnant women assigned to the high β-HCG group and 61,375 pregnant women to the control group. The incidence of PIH in the high β-HCG group was higher than that in the control group ( OR = 2.11 , 95% CI [1.90, 2.35], Z = 13.85 , P < 0.00001 ). There was no heterogeneity among literatures ( χ 2 = 8.53 , P = 0.38 , I 2 = 6 % ), and thus there is no identified publication bias ( P > 0.05 ). The incidence of preterm birth in the high β-HCG group was higher than that in the control group ( OR = 2.11 , 95% CI [1.90, 2.35], Z = 13.85 , P < 0.00001 ). The analysis suggested no heterogeneity among included literatures ( χ 2 = 11.78 , P = 0.11 , I 2 = 41 % ) and no publication bias ( P > 0.05 ). Higher incidence of abortion was observed in the high β-HCG group compared with the control group ( OR = 2.80 , 95% CI [1.92, 4.09], Z = 5.32 , P < 0.00001 ). There was no heterogeneity among literatures ( χ 2 = 3.43 , P = 0.33 , I 2 = 13 % ) and no publication bias ( P > 0.05 ). The incidence of gestational diabetes was higher in the high β-HCG group than in the control group ( OR = 2.15 , 95% CI [1.05, 4.40], Z = 2.09 , P = 0.04 ). Heterogeneity was identified among literatures ( χ 2 = 47.01 , P < 0.00001 , I 2 = 87 % ). Sensitivity analysis showed that the results were not robust, and there was no publication bias ( P > 0.05 ). Compared with control, the incidence of IGUR was higher in the high β-HCG group ( OR = 2.70 , 95% CI [1.75, 4.19], Z = 4.45 , P < 0.0001 ) with no heterogeneity among literatures ( χ 2 = 3.92 , P = 0.14 , I 2 = 49 % ) and no publication bias ( P > 0.05 ). Conclusion. High levels of β-hCG during pregnancy in singleton women are associated with a high incidence of pregnancy complications and adverse pregnancy outcomes. Pregnant women with high levels of β-hCG should be monitored more closely, followed up, and given timely medical interventions to reduce the incidence of pregnancy complications and adverse outcomes.
Background. The relationship among elevated serum β-human chorionic gonadotropin (β-hCG), the incidence of pregnancy complications, and adverse pregnancy outcomes has been controversial. Differences in study design, subject bias due to demographic characteristics, and differences in local medical levels could contribute to inconsistent results. Methods. Literature searches were performed in PubMed, EMBASE, Medline, Central, China National Knowledge Infrastructure (CNKI), Wanfang, and China Science Digital Library (CSDL) databases. Inclusion criteria were as follows: (1) research subjects were singleton pregnant women; (2) the study is identified as cohort study; (3) the subjects were assigned to the high β-hCG group and control group according to whether the exposure factors increased β-hCG in the second trimester; (4) the observed outcomes include at least pregnancy-induced hypertension (PIH), diabetes (gestational diabetes mellitus, GMD), preterm delivery (PD), and intrauterine growth restriction (IUGR); and (5) the odds ratio (OR) and 95% confidence interval (CI) of exposure factors are calculated based on literature dataset. To determine the risk bias of selected literatures, Newcastle-Ottawa scale was applied. The chi-square test was further used for heterogeneity analysis. If heterogeneity was identified, subgroup analyses were then performed for source investigation. Results. A total of 13 literatures were included and analyzed, including 67,355 pregnant women and 5980 pregnant women assigned to the high β-HCG group and 61,375 pregnant women to the control group. The incidence of PIH in the high β-HCG group was higher than that in the control group ( OR = 2.11 , 95% CI [1.90, 2.35], Z = 13.85 , P < 0.00001 ). There was no heterogeneity among literatures ( χ 2 = 8.53 , P = 0.38 , I 2 = 6 % ), and thus there is no identified publication bias ( P > 0.05 ). The incidence of preterm birth in the high β-HCG group was higher than that in the control group ( OR = 2.11 , 95% CI [1.90, 2.35], Z = 13.85 , P < 0.00001 ). The analysis suggested no heterogeneity among included literatures ( χ 2 = 11.78 , P = 0.11 , I 2 = 41 % ) and no publication bias ( P > 0.05 ). Higher incidence of abortion was observed in the high β-HCG group compared with the control group ( OR = 2.80 , 95% CI [1.92, 4.09], Z = 5.32 , P < 0.00001 ). There was no heterogeneity among literatures ( χ 2 = 3.43 , P = 0.33 , I 2 = 13 % ) and no publication bias ( P > 0.05 ). The incidence of gestational diabetes was higher in the high β-HCG group than in the control group ( OR = 2.15 , 95% CI [1.05, 4.40], Z = 2.09 , P = 0.04 ). Heterogeneity was identified among literatures ( χ 2 = 47.01 , P < 0.00001 , I 2 = 87 % ). Sensitivity analysis showed that the results were not robust, and there was no publication bias ( P > 0.05 ). Compared with control, the incidence of IGUR was higher in the high β-HCG group ( OR = 2.70 , 95% CI [1.75, 4.19], Z = 4.45 , P < 0.0001 ) with no heterogeneity among literatures ( χ 2 = 3.92 , P = 0.14 , I 2 = 49 % ) and no publication bias ( P > 0.05 ). Conclusion. High levels of β-hCG during pregnancy in singleton women are associated with a high incidence of pregnancy complications and adverse pregnancy outcomes. Pregnant women with high levels of β-hCG should be monitored more closely, followed up, and given timely medical interventions to reduce the incidence of pregnancy complications and adverse outcomes.
How to obtain copies of this and other HTA programme reports An electronic version of this publication, in Adobe Acrobat format, is available for downloading free of charge for personal use from the HTA website (www.hta.ac.uk). A fully searchable CD-ROM is also available (see below).Printed copies of HTA monographs cost £20 each (post and packing free in the UK) to both public and private sector purchasers from our Despatch Agents.Non-UK purchasers will have to pay a small fee for post and packing. For European countries the cost is £2 per monograph and for the rest of the world £3 per monograph.You can order HTA monographs from our Despatch Agents:-fax (with credit card or official purchase order) -post (with credit card or official purchase order or cheque) -phone during office hours (credit card only).Additionally the HTA website allows you either to pay securely by credit card or to print out your order and then post or fax it. Contact details are as follows: Payment methods Paying by chequeIf you pay by cheque, the cheque must be in pounds sterling, made payable to Direct Mail Works Ltd and drawn on a bank with a UK address. Paying by credit cardThe following cards are accepted by phone, fax, post or via the website ordering pages: Delta, Eurocard, Mastercard, Solo, Switch and Visa. We advise against sending credit card details in a plain email. Paying by official purchase orderYou can post or fax these, but they must be from public bodies (i.e. NHS or universities) within the UK. We cannot at present accept purchase orders from commercial companies or from outside the UK. How do I get a copy of HTA on CD?Please use the form on the HTA website (www.hta.ac.uk/htacd.htm). Or contact Direct Mail Works (see contact details above) by email, post, fax or phone. HTA on CD is currently free of charge worldwide.The website also provides information about the HTA programme and lists the membership of the various committees. HTA NIHR Health Technology Assessment programmeT he Health Technology Assessment (HTA) programme, part of the National Institute for Health Research (NIHR), was set up in 1993. It produces high-quality research information on the effectiveness, costs and broader impact of health technologies for those who use, manage and provide care in the NHS. 'Health technologies' are broadly defined as all interventions used to promote health, prevent and treat disease, and improve rehabilitation and long-term care. The research findings from the HTA programme directly influence decision-making bodies such as the National Institute for Health and Clinical Excellence (NICE) and the National Screening Committee (NSC). HTA findings also help to improve the quality of clinical practice in the NHS indirectly in that they form a key component of the 'National Knowledge Service'. The HTA programme is needs led in that it fills gaps in the evidence needed by the NHS. There are three routes to the start of projects. First is the commissioned route. Suggestions for research are actively sought from people working in t...
The aim of our study was to analyze the distribution of biochemical markers (free-â hCG and PAPP-A) and nuchal translucency (NT) values and their deviation from expected median in our screening program. NT, free-â hCG and PAPP-A values were measured in first trimester sera of 1313 singleton pregnant women. The age (mean ±standard deviation) of pregnant women at the time of screening was 28.94±4.95 years and the gestational age was 87.66±4.74 days. The value of NT (median±standard error of mean) was 0.87±0.01 multiple of median corrected (MoMc), of free-β hCG was 1.07±0.02 MoMc and of PAPP-A was 1.06±0.01 MoMc. Since the huge majority of pregnant women carried a healthy fetus it was assumed that the median value of measurements was equal to 1 MoMc and the deviation from median was equal to null. Our results showed that the greatest deviation from the expected median (-0.13 MoMc) was recorded for the NT measurement while the deviation for the free-â hCG and PAPP-A values was 0.07 respectively 0.06. In conclusion the main disturbing factor in calculating the aneuploidy risk was the measurement of NT. A systematic audit of laboratory and ultrasound measurement is necessary.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.