Genetic variations of MTHFR gene and their association with preterm birth in Korean women

The MTHFR gene encodes the methylenetetrahydrofolate reductase known to be involved in the homocysteine–methionine pathway. It has been reported that the deficiency of MTHFR activity may cause hyperhomocysteinemia which results in adverse pregnancy outcomes. Previous studies reported a correlation b...

Full description

Saved in:
Bibliographic Details
Published inMedicina (Kaunas, Lithuania) Vol. 53; no. 6; pp. 380 - 385
Main Authors Hwang, In Wook, Kang, Yun Dan, Kwon, Bit Na, Hong, Jun Ho, Han, Seung Hun, Kim, Jong Soo, Park, Jin Wan, Jin, Han Jun
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Sp. z o.o 01.01.2017
MDPI AG
Subjects
Online AccessGet full text
ISSN1010-660X
1648-9144
1648-9144
DOI10.1016/j.medici.2018.01.001

Cover

Abstract The MTHFR gene encodes the methylenetetrahydrofolate reductase known to be involved in the homocysteine–methionine pathway. It has been reported that the deficiency of MTHFR activity may cause hyperhomocysteinemia which results in adverse pregnancy outcomes. Previous studies reported a correlation between the MTHFR gene polymorphisms (677 T/C and 1298 A/C) and lower MTHFR activity and its association with preterm birth in various populations. Since these results were conflicting, we analyzed the genetic association of MTHFR gene 677 T/C and 1298 A/C polymorphisms with preterm birth in Korean women. The subjects for case–control study were collected a total of 226 Korean women (98 preterm-birth patients and 128 controls). Genotype frequency differences between the case and the control were assessed using chi-square tests. Mann–Whitney t-test was used to estimate the effects of 1298 A/C genotype on clinicopathological characteristics (systolic blood pressure, diastolic blood pressure, birth weight, and gestational age at delivery) in preterm-birth patients. Our results showed that the MTHFR 677 C/T polymorphism was significantly associated with preterm-birth patients in the analysis of genotype frequency (P=0.044) and the over-dominant model (OR=0.54; 95% CI, 0.320–0.920; P=0.023). The recessive model showed a marginal trend toward significance (OR=0.47; 95% CI, 0.220–1.010; P=0.046). The 1298 A/C polymorphism was also associated with reduced preterm-birth risk in the recessive model (P=0.032). In the correlation analysis, the 1298 C allele was significantly associated with increasing of gestational age at delivery in preterm-birth patients (P=0.034). Our findings suggested that the MTHFR gene 677 C/T and 1298 A/C polymorphisms might have protective effects for preterm birth in the Korean women.
AbstractList The MTHFR gene encodes the methylenetetrahydrofolate reductase known to be involved in the homocysteine-methionine pathway. It has been reported that the deficiency of MTHFR activity may cause hyperhomocysteinemia which results in adverse pregnancy outcomes. Previous studies reported a correlation between the MTHFR gene polymorphisms (677 T/C and 1298 A/C) and lower MTHFR activity and its association with preterm birth in various populations. Since these results were conflicting, we analyzed the genetic association of MTHFR gene 677 T/C and 1298 A/C polymorphisms with preterm birth in Korean women.BACKGROUND AND OBJECTIVEThe MTHFR gene encodes the methylenetetrahydrofolate reductase known to be involved in the homocysteine-methionine pathway. It has been reported that the deficiency of MTHFR activity may cause hyperhomocysteinemia which results in adverse pregnancy outcomes. Previous studies reported a correlation between the MTHFR gene polymorphisms (677 T/C and 1298 A/C) and lower MTHFR activity and its association with preterm birth in various populations. Since these results were conflicting, we analyzed the genetic association of MTHFR gene 677 T/C and 1298 A/C polymorphisms with preterm birth in Korean women.The subjects for case-control study were collected a total of 226 Korean women (98 preterm-birth patients and 128 controls). Genotype frequency differences between the case and the control were assessed using chi-square tests. Mann-Whitney t-test was used to estimate the effects of 1298 A/C genotype on clinicopathological characteristics (systolic blood pressure, diastolic blood pressure, birth weight, and gestational age at delivery) in preterm-birth patients.MATERIALS AND METHODSThe subjects for case-control study were collected a total of 226 Korean women (98 preterm-birth patients and 128 controls). Genotype frequency differences between the case and the control were assessed using chi-square tests. Mann-Whitney t-test was used to estimate the effects of 1298 A/C genotype on clinicopathological characteristics (systolic blood pressure, diastolic blood pressure, birth weight, and gestational age at delivery) in preterm-birth patients.Our results showed that the MTHFR 677 C/T polymorphism was significantly associated with preterm-birth patients in the analysis of genotype frequency (P=0.044) and the over-dominant model (OR=0.54; 95% CI, 0.320-0.920; P=0.023). The recessive model showed a marginal trend toward significance (OR=0.47; 95% CI, 0.220-1.010; P=0.046). The 1298 A/C polymorphism was also associated with reduced preterm-birth risk in the recessive model (P=0.032). In the correlation analysis, the 1298 C allele was significantly associated with increasing of gestational age at delivery in preterm-birth patients (P=0.034).RESULTSOur results showed that the MTHFR 677 C/T polymorphism was significantly associated with preterm-birth patients in the analysis of genotype frequency (P=0.044) and the over-dominant model (OR=0.54; 95% CI, 0.320-0.920; P=0.023). The recessive model showed a marginal trend toward significance (OR=0.47; 95% CI, 0.220-1.010; P=0.046). The 1298 A/C polymorphism was also associated with reduced preterm-birth risk in the recessive model (P=0.032). In the correlation analysis, the 1298 C allele was significantly associated with increasing of gestational age at delivery in preterm-birth patients (P=0.034).Our findings suggested that the MTHFR gene 677 C/T and 1298 A/C polymorphisms might have protective effects for preterm birth in the Korean women.CONCLUSIONSOur findings suggested that the MTHFR gene 677 C/T and 1298 A/C polymorphisms might have protective effects for preterm birth in the Korean women.
Background and objective: The MTHFR gene encodes the methylenetetrahydrofolate reductase known to be involved in the homocysteine–methionine pathway. It has been reported that the deficiency of MTHFR activity may cause hyperhomocysteinemia which results in adverse pregnancy outcomes. Previous studies reported a correlation between the MTHFR gene polymorphisms (677 T/C and 1298 A/C) and lower MTHFR activity and its association with preterm birth in various populations. Since these results were conflicting, we analyzed the genetic association of MTHFR gene 677 T/C and 1298 A/C polymorphisms with preterm birth in Korean women. Materials and methods: The subjects for case–control study were collected a total of 226 Korean women (98 preterm-birth patients and 128 controls). Genotype frequency differences between the case and the control were assessed using chi-square tests. Mann–Whitney t-test was used to estimate the effects of 1298 A/C genotype on clinicopathological characteristics (systolic blood pressure, diastolic blood pressure, birth weight, and gestational age at delivery) in preterm-birth patients. Results: Our results showed that the MTHFR 677 C/T polymorphism was significantly associated with preterm-birth patients in the analysis of genotype frequency (P = 0.044) and the over-dominant model (OR = 0.54; 95% CI, 0.320–0.920; P = 0.023). The recessive model showed a marginal trend toward significance (OR = 0.47; 95% CI, 0.220–1.010; P = 0.046). The 1298 A/C polymorphism was also associated with reduced preterm-birth risk in the recessive model (P = 0.032). In the correlation analysis, the 1298 C allele was significantly associated with increasing of gestational age at delivery in preterm-birth patients (P = 0.034). Conclusions: Our findings suggested that the MTHFR gene 677 C/T and 1298 A/C polymorphisms might have protective effects for preterm birth in the Korean women. Keywords: Preterm birth, MTHFR, Polymorphism, Korean women, Genetic association
The MTHFR gene encodes the methylenetetrahydrofolate reductase known to be involved in the homocysteine-methionine pathway. It has been reported that the deficiency of MTHFR activity may cause hyperhomocysteinemia which results in adverse pregnancy outcomes. Previous studies reported a correlation between the MTHFR gene polymorphisms (677 T/C and 1298 A/C) and lower MTHFR activity and its association with preterm birth in various populations. Since these results were conflicting, we analyzed the genetic association of MTHFR gene 677 T/C and 1298 A/C polymorphisms with preterm birth in Korean women. The subjects for case-control study were collected a total of 226 Korean women (98 preterm-birth patients and 128 controls). Genotype frequency differences between the case and the control were assessed using chi-square tests. Mann-Whitney t-test was used to estimate the effects of 1298 A/C genotype on clinicopathological characteristics (systolic blood pressure, diastolic blood pressure, birth weight, and gestational age at delivery) in preterm-birth patients. Our results showed that the MTHFR 677 C/T polymorphism was significantly associated with preterm-birth patients in the analysis of genotype frequency (P=0.044) and the over-dominant model (OR=0.54; 95% CI, 0.320-0.920; P=0.023). The recessive model showed a marginal trend toward significance (OR=0.47; 95% CI, 0.220-1.010; P=0.046). The 1298 A/C polymorphism was also associated with reduced preterm-birth risk in the recessive model (P=0.032). In the correlation analysis, the 1298 C allele was significantly associated with increasing of gestational age at delivery in preterm-birth patients (P=0.034). Our findings suggested that the MTHFR gene 677 C/T and 1298 A/C polymorphisms might have protective effects for preterm birth in the Korean women.
Author Hong, Jun Ho
Kwon, Bit Na
Jin, Han Jun
Park, Jin Wan
Hwang, In Wook
Kang, Yun Dan
Han, Seung Hun
Kim, Jong Soo
Author_xml – sequence: 1
  givenname: In Wook
  surname: Hwang
  fullname: Hwang, In Wook
  organization: Department of Biological Sciences, College of Natural Science, Dankook University, Cheonan, Republic of Korea
– sequence: 2
  givenname: Yun Dan
  surname: Kang
  fullname: Kang, Yun Dan
  organization: Department of Obstetrics and Gynecology, Dankook University Hospital, Cheonan, Republic of Korea
– sequence: 3
  givenname: Bit Na
  surname: Kwon
  fullname: Kwon, Bit Na
  organization: Department of Biological Sciences, College of Natural Science, Dankook University, Cheonan, Republic of Korea
– sequence: 4
  givenname: Jun Ho
  surname: Hong
  fullname: Hong, Jun Ho
  organization: Department of Biological Sciences, College of Natural Science, Dankook University, Cheonan, Republic of Korea
– sequence: 5
  givenname: Seung Hun
  surname: Han
  fullname: Han, Seung Hun
  organization: Department of Microbiology, College of Natural Science, Dankook University, Cheonan, Republic of Korea
– sequence: 6
  givenname: Jong Soo
  surname: Kim
  fullname: Kim, Jong Soo
  organization: Department of Obstetrics and Gynecology, Dankook University Hospital, Cheonan, Republic of Korea
– sequence: 7
  givenname: Jin Wan
  surname: Park
  fullname: Park, Jin Wan
  email: parkdkog@dankook.ac.kr
  organization: Department of Obstetrics and Gynecology, Dankook University Hospital, Cheonan, Republic of Korea
– sequence: 8
  givenname: Han Jun
  surname: Jin
  fullname: Jin, Han Jun
  email: jins4658@dankook.ac.kr
  organization: Department of Biological Sciences, College of Natural Science, Dankook University, Cheonan, Republic of Korea
BackLink https://www.ncbi.nlm.nih.gov/pubmed/29428336$$D View this record in MEDLINE/PubMed
BookMark eNqFUclu1TAUtVARHeAPEPKSTYJvPMRhgYQqOogiJFQkWFmOc9P6KYkftl8Rf49f07JgASsP9wz2OcfkYAkLEvISWA0M1JtNPePgna8bBrpmUDMGT8gRKKGrDoQ4KHsGrFKKfTskxyltGOONbJtn5LDpRKM5V0fk-zkumL2jdzZ6m31YEg0j_XR9cfaF3pQZtctA8y36SG1Kwa0g-tPnW7qNmDHOtPexnPxCP4aItgzDjMtz8nS0U8IXD-sJ-Xr24fr0orr6fH55-v6qcqIVuXJybLkUoKRGxa3r1KA5gFKj1AJEeSRnugVonWtbp0fdMAkSnWp627O24yfkctUdgt2YbfSzjb9MsN7cX4R4Y2wsP5zQIHSis1yxjpeAilaPTCjbd1ZyHNAVrder1jaGHztM2cw-OZwmu2DYJdOUjAWTSu5tXz1Ad30p4o_xY7QF8HYFuBhSijga5_N9eDlaPxlgZt-j2Zi1R7Pv0TAwxaOQxV_kR_3_0N6tNCyB33mMJjmPiyvIiC6XRPy_BX4Dhwi2cQ
CitedBy_id crossref_primary_10_4103_mgmj_mgmj_220_22
crossref_primary_10_5582_bst_2021_01306
crossref_primary_10_3390_medicina60122028
crossref_primary_10_1007_s00404_022_06701_2
crossref_primary_10_1186_s43042_023_00385_2
crossref_primary_10_29328_journal_cjog_1001182
crossref_primary_10_4103_sjamf_sjamf_38_18
crossref_primary_10_1007_s43032_023_01287_9
crossref_primary_10_1016_j_humgen_2023_201190
crossref_primary_10_1186_s40246_023_00566_5
crossref_primary_10_3390_nu14102108
crossref_primary_10_1002_ijgo_16056
crossref_primary_10_1515_jpm_2022_0119
Cites_doi 10.1016/j.amjmed.2004.01.019
10.3961/jpmph.16.022
10.1161/STROKEAHA.115.011545
10.1016/j.mgene.2014.12.002
10.1007/s00404-017-4322-z
10.1046/j.1365-2141.2001.03140.x
10.4238/2015.February.2.9
10.1371/journal.pone.0064446
10.1097/AOG.0000000000001678
10.3389/fphys.2017.00104
10.3758/BF03203630
10.1016/j.hlc.2014.01.010
10.1371/journal.pmed.1001274
10.1093/aje/kwg024
10.4103/0974-1208.97779
10.1016/j.ajog.2009.05.060
10.1155/2014/164081
10.1183/09031936.03.00061703
10.1007/s11011-011-9256-8
10.1159/000356774
10.1111/aogs.12789
10.1016/j.ajog.2006.07.024
10.2471/BLT.08.062554
10.1016/j.neulet.2016.01.031
10.1007/s13258-017-0552-5
10.1093/aje/kwh066
ContentType Journal Article
Copyright 2018 The Lithuanian University of Health Sciences
Copyright © 2018 The Lithuanian University of Health Sciences. Production and hosting by Elsevier Sp. z o.o. All rights reserved.
Copyright_xml – notice: 2018 The Lithuanian University of Health Sciences
– notice: Copyright © 2018 The Lithuanian University of Health Sciences. Production and hosting by Elsevier Sp. z o.o. All rights reserved.
DBID 6I.
AAFTH
AAYXX
CITATION
NPM
7X8
DOA
DOI 10.1016/j.medici.2018.01.001
DatabaseName ScienceDirect Open Access Titles
Elsevier:ScienceDirect:Open Access
CrossRef
PubMed
MEDLINE - Academic
DOAJ
DatabaseTitle CrossRef
PubMed
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic

PubMed

Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1648-9144
EndPage 385
ExternalDocumentID oai_doaj_org_article_e1949a360931448f8be046ab9a53edec
29428336
10_1016_j_medici_2018_01_001
S1010660X1830003X
Genre Journal Article
GroupedDBID 0R~
0SF
29M
2WC
4.4
457
53G
5GY
5VS
6I.
7X7
8FI
8FJ
AACTN
AADQD
AAEDT
AAEDW
AAFTH
AAFWJ
AAIKJ
AALRI
AAXUO
ABMAC
ABUWG
ACGFS
ADBBV
ADEZE
AFKRA
AFPKN
AFZYC
AGHFR
AHDRD
AITUG
ALMA_UNASSIGNED_HOLDINGS
AMRAJ
AOIJS
BAWUL
BCNDV
BENPR
CCPQU
DIK
EBS
EJD
EMOBN
F5P
FDB
FYUFA
GROUPED_DOAJ
HMCUK
HYE
IAO
IPNFZ
KQ8
M41
MODMG
NCXOZ
O9-
OK1
PIMPY
RIG
ROL
RPM
SSZ
UKHRP
XSB
AAYWO
AAYXX
ADVLN
ALIPV
CITATION
IHR
ITC
OVT
PGMZT
PHGZM
PHGZT
NPM
7X8
ID FETCH-LOGICAL-c474t-c5f73541658e63ac96d831166f584143363087117cc77c8f820515ec62bab0793
IEDL.DBID DOA
ISSN 1010-660X
1648-9144
IngestDate Wed Aug 27 01:18:23 EDT 2025
Fri Sep 05 02:41:02 EDT 2025
Thu Apr 03 07:02:32 EDT 2025
Tue Jul 01 03:11:40 EDT 2025
Thu Apr 24 22:54:18 EDT 2025
Fri Feb 23 02:27:18 EST 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 6
Keywords MTHFR
Preterm birth
Genetic association
Korean women
Polymorphism
Language English
License This is an open access article under the CC BY-NC-ND license.
http://creativecommons.org/licenses/by-nc-nd/4.0
http://www.elsevier.com/tdm/userlicense/1.0
Copyright © 2018 The Lithuanian University of Health Sciences. Production and hosting by Elsevier Sp. z o.o. All rights reserved.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c474t-c5f73541658e63ac96d831166f584143363087117cc77c8f820515ec62bab0793
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://doaj.org/article/e1949a360931448f8be046ab9a53edec
PMID 29428336
PQID 2001405659
PQPubID 23479
PageCount 6
ParticipantIDs doaj_primary_oai_doaj_org_article_e1949a360931448f8be046ab9a53edec
proquest_miscellaneous_2001405659
pubmed_primary_29428336
crossref_citationtrail_10_1016_j_medici_2018_01_001
crossref_primary_10_1016_j_medici_2018_01_001
elsevier_sciencedirect_doi_10_1016_j_medici_2018_01_001
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2017-01-01
PublicationDateYYYYMMDD 2017-01-01
PublicationDate_xml – month: 01
  year: 2017
  text: 2017-01-01
  day: 01
PublicationDecade 2010
PublicationPlace Netherlands
PublicationPlace_xml – name: Netherlands
PublicationTitle Medicina (Kaunas, Lithuania)
PublicationTitleAlternate Medicina (Kaunas)
PublicationYear 2017
Publisher Elsevier Sp. z o.o
MDPI AG
Publisher_xml – name: Elsevier Sp. z o.o
– name: MDPI AG
References Kang, Lee, Hong, Chung, Oh, Kim (bib0265) 2010; 3
Chan (bib0335) 2014; 2014
Engel, Olshan, Siega-Riz, Savitz, Chanock (bib0290) 2006; 195
Tiwari, Bose, Das, Das, Datta, Bose (bib0285) 2015; 3
Tellapragada, Eshwara, Bhat, Acharya, Kamath, Bhat (bib0200) 2016; 49
Gargano, Holzman, Senagore, Reuss, Pathak, Friderici (bib0240) 2009; 201
Erdfelder, Faul, Buchner (bib0325) 1996; 28
Chakraborty, Goswami, Rajani, Sharma, Kabit, Chakravarty (bib0220) 2013; 8
Vieira, Bayram, Seymen, Sencak, Lippert, Modesto (bib0330) 2017; 8
Wang, Liu, Wang, Dai, Tao, Wang (bib0195) 2015; 14
Oh, Kim, Jang, Kim, Lee, Lee (bib0315) 2007; 27
Du, Yang, Gong, Guan, Mei, Li (bib0280) 2013; 34
Beck, Wojdyla, Say, Betran, Merialdi, Requejo (bib0185) 2010; 88
Sharp, Little (bib0300) 2004; 159
Böttiger, Hurtig-Wennlöf, Sjöström, Yngve, Nilsson (bib0230) 2007; 19
Wu, Zhu, Geng, Liu, Cui, Gao (bib0215) 2017; 295
Rutten-Jacobs, Traylor, Adib-Samii, Thijs, Sudlow, Rothwell (bib0225) 2016; 47
Franco, Simoes, Tone, Gabellini, Zago, Falcao (bib0295) 2001; 115
Nurk, Tell, Refsum, Ueland, Vollset (bib0245) 2004; 117
Engelstad, Roghair, Calarge, Colaizy, Stuart, Haskell (bib0250) 2014; 105
Robien, Ulrich (bib0275) 2003; 157
Smith (bib0175) 2012; 9
Blencowe, Cousens, Oestergaard, Chou, Moller, Narwal (bib0180) 2012; 9
Chen, Chen, Zhu, Zhang, Wu (bib0205) 2016; 95
Nan, Li (bib0210) 2015; 8
Chao, Wei, Huang, Yang (bib0255) 2014; 23
Yuan, Song, Deng, Xiong, Yang, Deng (bib0305) 2016; 616
Park, Kim, Lim (bib0190) 2016; 0
Deb, Arora, Meitei, Gupta, Verma, Saraswathy (bib0310) 2011; 26
Suresh, Chandrashekara (bib0320) 2012; 5
Cristalli, Zannini, Comai, Baraldi, Cuna, Cappuccilli (bib0235) 2017; 39
Ogus, Yoldas, Ozdemir, Uquz, Olcen, Keser (bib0260) 2004; 23
Rady, Szucs, Grady, Hudnall, Kellner, Nitowsky (bib0270) 2002; 107
Hermesch, Allshouse, Heyborne (bib0340) 2016; 128
Suresh (10.1016/j.medici.2018.01.001_bib0320) 2012; 5
Yuan (10.1016/j.medici.2018.01.001_bib0305) 2016; 616
Chan (10.1016/j.medici.2018.01.001_bib0335) 2014; 2014
Smith (10.1016/j.medici.2018.01.001_bib0175) 2012; 9
Deb (10.1016/j.medici.2018.01.001_bib0310) 2011; 26
Chakraborty (10.1016/j.medici.2018.01.001_bib0220) 2013; 8
Hermesch (10.1016/j.medici.2018.01.001_bib0340) 2016; 128
Chen (10.1016/j.medici.2018.01.001_bib0205) 2016; 95
Tiwari (10.1016/j.medici.2018.01.001_bib0285) 2015; 3
Erdfelder (10.1016/j.medici.2018.01.001_bib0325) 1996; 28
Beck (10.1016/j.medici.2018.01.001_bib0185) 2010; 88
Sharp (10.1016/j.medici.2018.01.001_bib0300) 2004; 159
Chao (10.1016/j.medici.2018.01.001_bib0255) 2014; 23
Robien (10.1016/j.medici.2018.01.001_bib0275) 2003; 157
Oh (10.1016/j.medici.2018.01.001_bib0315) 2007; 27
Park (10.1016/j.medici.2018.01.001_bib0190) 2016; 0
Wang (10.1016/j.medici.2018.01.001_bib0195) 2015; 14
Gargano (10.1016/j.medici.2018.01.001_bib0240) 2009; 201
Tellapragada (10.1016/j.medici.2018.01.001_bib0200) 2016; 49
Rady (10.1016/j.medici.2018.01.001_bib0270) 2002; 107
Engel (10.1016/j.medici.2018.01.001_bib0290) 2006; 195
Wu (10.1016/j.medici.2018.01.001_bib0215) 2017; 295
Du (10.1016/j.medici.2018.01.001_bib0280) 2013; 34
Cristalli (10.1016/j.medici.2018.01.001_bib0235) 2017; 39
Nurk (10.1016/j.medici.2018.01.001_bib0245) 2004; 117
Rutten-Jacobs (10.1016/j.medici.2018.01.001_bib0225) 2016; 47
Vieira (10.1016/j.medici.2018.01.001_bib0330) 2017; 8
Nan (10.1016/j.medici.2018.01.001_bib0210) 2015; 8
Böttiger (10.1016/j.medici.2018.01.001_bib0230) 2007; 19
Ogus (10.1016/j.medici.2018.01.001_bib0260) 2004; 23
Kang (10.1016/j.medici.2018.01.001_bib0265) 2010; 3
Engelstad (10.1016/j.medici.2018.01.001_bib0250) 2014; 105
Franco (10.1016/j.medici.2018.01.001_bib0295) 2001; 115
Blencowe (10.1016/j.medici.2018.01.001_bib0180) 2012; 9
References_xml – volume: 3
  start-page: 74
  year: 2010
  end-page: 77
  ident: bib0265
  article-title: Polymorphisms of 5,10-methylenetetrahydrofolate reductase and thymidylate synthase in squamous cell carcinoma and basal cell carcinoma of the skin
  publication-title: Mol Med Rep
– volume: 295
  start-page: 1105
  year: 2017
  end-page: 1118
  ident: bib0215
  article-title: Genetic polymorphism of MTHFR C677T with preterm birth and low birth weight susceptibility: a meta-analysis
  publication-title: Arch Gynecol Obstet
– volume: 3
  start-page: 31
  year: 2015
  end-page: 42
  ident: bib0285
  article-title: MTHFR (C677T) polymorphism and PR (PROGINS) mutation as genetic factors for preterm delivery, fetal death and low birth weight: a Northeast Indian population based study
  publication-title: Meta Gene
– volume: 115
  start-page: 616
  year: 2001
  end-page: 618
  ident: bib0295
  article-title: The methylenetetrahydrofolate reductase C677T gene polymorphism decreases the risk of childhood acute lymphocytic leukaemia
  publication-title: Br J Haematol
– volume: 23
  start-page: 655
  year: 2014
  end-page: 660
  ident: bib0255
  article-title: Correlation between methyltetrahydrofolate reductase (MTHFR) polymorphisms and isolated patent ductus arteriosus in Taiwan
  publication-title: Heart Lung Circ
– volume: 14
  start-page: 850
  year: 2015
  end-page: 859
  ident: bib0195
  article-title: Association between SNPs in genes involved in folate metabolism and preterm birth risk
  publication-title: Genet Mol Res
– volume: 19
  start-page: 659
  year: 2007
  end-page: 665
  ident: bib0230
  article-title: Association of total plasma homocysteine with methylenetetrahydrofolate reductase genotypes 677C>T, 1298A>C, and 1793G>A and the corresponding haplotypes in Swedish children and adolescents
  publication-title: Int J Mol Med
– volume: 2014
  start-page: 164081
  year: 2014
  ident: bib0335
  article-title: Biochemical markers of spontaneous preterm birth in asymptomatic women
  publication-title: Biomed Res Int
– volume: 26
  start-page: 241
  year: 2011
  end-page: 246
  ident: bib0310
  article-title: Folate supplementation, MTHFR gene polymorphism and neural tube defects: a community based case control study in North India
  publication-title: Metab Brain Dis
– volume: 8
  start-page: e64446
  year: 2013
  ident: bib0220
  article-title: Recurrent pregnancy loss in polycystic ovary syndrome: role of hyperhomocysteinemia and insulin resistance
  publication-title: PLOS ONE
– volume: 201
  start-page: e1
  year: 2009
  end-page: e9
  ident: bib0240
  article-title: Polymorphisms in thrombophilia and renin–angiotensin system pathways, preterm delivery, and evidence of placental hemorrhage
  publication-title: Am J Obstet Gynecol
– volume: 128
  start-page: 1033
  year: 2016
  end-page: 1038
  ident: bib0340
  article-title: Body mass index and the spontaneous onset of parturition
  publication-title: Obstet Gynecol
– volume: 95
  start-page: 157
  year: 2016
  end-page: 165
  ident: bib0205
  article-title: Association of methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with preterm delivery and placental abruption: a systematic review and meta-analysis
  publication-title: AOGS
– volume: 27
  start-page: 3419
  year: 2007
  end-page: 3424
  ident: bib0315
  article-title: Association of the 5,10-methylenetetrahydrofolate reductase (MTHFR C677T and A1298C) polymorphisms in Korean patients with adult acute lymphoblastic leukemia
  publication-title: Anticancer Res
– volume: 105
  start-page: 149
  year: 2014
  end-page: 154
  ident: bib0250
  article-title: Perinatal outcomes of pregnancies complicated by maternal depression with or without
  publication-title: Neonatology
– volume: 23
  start-page: 219
  year: 2004
  end-page: 223
  ident: bib0260
  article-title: The Arg753GLn polymorphism of the human toll-like receptor 2 gene in tuberculosis disease
  publication-title: Eur Respir J
– volume: 5
  start-page: 7
  year: 2012
  end-page: 13
  ident: bib0320
  article-title: Sample size estimation and power analysis for clinical research studies
  publication-title: J Hum Reprod Sci
– volume: 49
  start-page: 165
  year: 2016
  end-page: 175
  ident: bib0200
  article-title: Risk factors for preterm birth and low birth weight among pregnant Indian women: a Hospital-based Prospective Study
  publication-title: J Prev Med Public Health
– volume: 195
  year: 2006
  ident: bib0290
  article-title: Polymorphisms in folate metabolizing genes and risk for spontaneous preterm and small-for-gestational age birth
  publication-title: Am J Obstet Gynecol
– volume: 616
  start-page: 26
  year: 2016
  end-page: 31
  ident: bib0305
  article-title: Association of the MTHFR rs1801131 and rs1801133 variants in sporadic Parkinson's disease patients
  publication-title: Neurosci Lett
– volume: 107
  start-page: 162
  year: 2002
  end-page: 168
  ident: bib0270
  article-title: Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A
  publication-title: Am J Epidemiol
– volume: 39
  start-page: 689
  year: 2017
  end-page: 699
  ident: bib0235
  article-title: Methylenetetrahydrofolate reductase, MTHFR, polymorphisms and prediposition to different multifactorial disorders
  publication-title: Genes Genomics
– volume: 34
  start-page: 894
  year: 2013
  end-page: 899
  ident: bib0280
  article-title: Relationship of plasma homocysteine levels, folate levels and MTHFR gene polymorphisms with premature delivery
  publication-title: J Sun Yat-sen Univ (Med Sci)
– volume: 88
  start-page: 31
  year: 2010
  end-page: 38
  ident: bib0185
  article-title: The worldwide incidence of preterm birth: a systematic review of maternal mortality and morbidity
  publication-title: Bull World Health Organ
– volume: 47
  start-page: 646
  year: 2016
  end-page: 651
  ident: bib0225
  article-title: Association of MTHFR C677T genotype with ischemic stroke is confined to cerebral small vessel disease subtype
  publication-title: Stroke
– volume: 8
  start-page: 104
  year: 2017
  ident: bib0330
  article-title: In vitro acid-mediated initial dental enamel loss is associated with genetic variants previously linked to caries experience
  publication-title: Front Physiol
– volume: 0
  start-page: 221
  year: 2016
  end-page: 227
  ident: bib0190
  article-title: Contribution of maternal age distribution to incidence of preterm birth; 1997∼99 and 2012∼14 singleton birth certificated data of Korea
  publication-title: J Korean Soc Matern Child Health
– volume: 159
  start-page: 423
  year: 2004
  end-page: 443
  ident: bib0300
  article-title: Polymorphisms in genes involved in folate metabolism and colorectal neoplasia: a HuGE review
  publication-title: Am J Epidemiol
– volume: 9
  start-page: 379
  year: 2012
  ident: bib0180
  article-title: National, regional, and worldwide estimates of preterm birth rates in the year 2010 with timetrends since 1990 for selected countries: a systematic analysis and implication
  publication-title: Lancet
– volume: 117
  start-page: 26
  year: 2004
  end-page: 31
  ident: bib0245
  article-title: Associations between maternal methylenetetrahydrofolate reductase polymorphisms and adverse outcomes of pregnancy: the Hordaland Homocysteine Study
  publication-title: Am J Med
– volume: 9
  start-page: e1001274
  year: 2012
  ident: bib0175
  article-title: Researching new methods of screening for adverse pregnancy outcome: lessons from pre-eclampsia
  publication-title: PLoS Med
– volume: 8
  start-page: 7397
  year: 2015
  end-page: 7402
  ident: bib0210
  article-title: MTHFR genetic polymorphism increases the risk of preterm delivery
  publication-title: Int J Clin Exp Pathol
– volume: 157
  start-page: 571
  year: 2003
  end-page: 582
  ident: bib0275
  article-title: 5,10-Methylenetetrahydrofolate reductase polymorphisms and leukemia risk: a HuGE minireview
  publication-title: Am J Epidemiol
– volume: 28
  start-page: 1
  year: 1996
  end-page: 11
  ident: bib0325
  article-title: GPOWER: a general power analysis program
  publication-title: Behav Res Methods
– volume: 19
  start-page: 659
  year: 2007
  ident: 10.1016/j.medici.2018.01.001_bib0230
  article-title: Association of total plasma homocysteine with methylenetetrahydrofolate reductase genotypes 677C>T, 1298A>C, and 1793G>A and the corresponding haplotypes in Swedish children and adolescents
  publication-title: Int J Mol Med
– volume: 117
  start-page: 26
  year: 2004
  ident: 10.1016/j.medici.2018.01.001_bib0245
  article-title: Associations between maternal methylenetetrahydrofolate reductase polymorphisms and adverse outcomes of pregnancy: the Hordaland Homocysteine Study
  publication-title: Am J Med
  doi: 10.1016/j.amjmed.2004.01.019
– volume: 49
  start-page: 165
  year: 2016
  ident: 10.1016/j.medici.2018.01.001_bib0200
  article-title: Risk factors for preterm birth and low birth weight among pregnant Indian women: a Hospital-based Prospective Study
  publication-title: J Prev Med Public Health
  doi: 10.3961/jpmph.16.022
– volume: 47
  start-page: 646
  year: 2016
  ident: 10.1016/j.medici.2018.01.001_bib0225
  article-title: Association of MTHFR C677T genotype with ischemic stroke is confined to cerebral small vessel disease subtype
  publication-title: Stroke
  doi: 10.1161/STROKEAHA.115.011545
– volume: 27
  start-page: 3419
  year: 2007
  ident: 10.1016/j.medici.2018.01.001_bib0315
  article-title: Association of the 5,10-methylenetetrahydrofolate reductase (MTHFR C677T and A1298C) polymorphisms in Korean patients with adult acute lymphoblastic leukemia
  publication-title: Anticancer Res
– volume: 0
  start-page: 221
  year: 2016
  ident: 10.1016/j.medici.2018.01.001_bib0190
  article-title: Contribution of maternal age distribution to incidence of preterm birth; 1997∼99 and 2012∼14 singleton birth certificated data of Korea
  publication-title: J Korean Soc Matern Child Health
– volume: 3
  start-page: 31
  year: 2015
  ident: 10.1016/j.medici.2018.01.001_bib0285
  article-title: MTHFR (C677T) polymorphism and PR (PROGINS) mutation as genetic factors for preterm delivery, fetal death and low birth weight: a Northeast Indian population based study
  publication-title: Meta Gene
  doi: 10.1016/j.mgene.2014.12.002
– volume: 295
  start-page: 1105
  year: 2017
  ident: 10.1016/j.medici.2018.01.001_bib0215
  article-title: Genetic polymorphism of MTHFR C677T with preterm birth and low birth weight susceptibility: a meta-analysis
  publication-title: Arch Gynecol Obstet
  doi: 10.1007/s00404-017-4322-z
– volume: 115
  start-page: 616
  year: 2001
  ident: 10.1016/j.medici.2018.01.001_bib0295
  article-title: The methylenetetrahydrofolate reductase C677T gene polymorphism decreases the risk of childhood acute lymphocytic leukaemia
  publication-title: Br J Haematol
  doi: 10.1046/j.1365-2141.2001.03140.x
– volume: 14
  start-page: 850
  year: 2015
  ident: 10.1016/j.medici.2018.01.001_bib0195
  article-title: Association between SNPs in genes involved in folate metabolism and preterm birth risk
  publication-title: Genet Mol Res
  doi: 10.4238/2015.February.2.9
– volume: 8
  start-page: e64446
  year: 2013
  ident: 10.1016/j.medici.2018.01.001_bib0220
  article-title: Recurrent pregnancy loss in polycystic ovary syndrome: role of hyperhomocysteinemia and insulin resistance
  publication-title: PLOS ONE
  doi: 10.1371/journal.pone.0064446
– volume: 128
  start-page: 1033
  year: 2016
  ident: 10.1016/j.medici.2018.01.001_bib0340
  article-title: Body mass index and the spontaneous onset of parturition
  publication-title: Obstet Gynecol
  doi: 10.1097/AOG.0000000000001678
– volume: 8
  start-page: 104
  year: 2017
  ident: 10.1016/j.medici.2018.01.001_bib0330
  article-title: In vitro acid-mediated initial dental enamel loss is associated with genetic variants previously linked to caries experience
  publication-title: Front Physiol
  doi: 10.3389/fphys.2017.00104
– volume: 28
  start-page: 1
  year: 1996
  ident: 10.1016/j.medici.2018.01.001_bib0325
  article-title: GPOWER: a general power analysis program
  publication-title: Behav Res Methods
  doi: 10.3758/BF03203630
– volume: 23
  start-page: 655
  year: 2014
  ident: 10.1016/j.medici.2018.01.001_bib0255
  article-title: Correlation between methyltetrahydrofolate reductase (MTHFR) polymorphisms and isolated patent ductus arteriosus in Taiwan
  publication-title: Heart Lung Circ
  doi: 10.1016/j.hlc.2014.01.010
– volume: 9
  start-page: e1001274
  year: 2012
  ident: 10.1016/j.medici.2018.01.001_bib0175
  article-title: Researching new methods of screening for adverse pregnancy outcome: lessons from pre-eclampsia
  publication-title: PLoS Med
  doi: 10.1371/journal.pmed.1001274
– volume: 157
  start-page: 571
  year: 2003
  ident: 10.1016/j.medici.2018.01.001_bib0275
  article-title: 5,10-Methylenetetrahydrofolate reductase polymorphisms and leukemia risk: a HuGE minireview
  publication-title: Am J Epidemiol
  doi: 10.1093/aje/kwg024
– volume: 5
  start-page: 7
  year: 2012
  ident: 10.1016/j.medici.2018.01.001_bib0320
  article-title: Sample size estimation and power analysis for clinical research studies
  publication-title: J Hum Reprod Sci
  doi: 10.4103/0974-1208.97779
– volume: 201
  start-page: e1
  year: 2009
  ident: 10.1016/j.medici.2018.01.001_bib0240
  article-title: Polymorphisms in thrombophilia and renin–angiotensin system pathways, preterm delivery, and evidence of placental hemorrhage
  publication-title: Am J Obstet Gynecol
  doi: 10.1016/j.ajog.2009.05.060
– volume: 2014
  start-page: 164081
  year: 2014
  ident: 10.1016/j.medici.2018.01.001_bib0335
  article-title: Biochemical markers of spontaneous preterm birth in asymptomatic women
  publication-title: Biomed Res Int
  doi: 10.1155/2014/164081
– volume: 23
  start-page: 219
  year: 2004
  ident: 10.1016/j.medici.2018.01.001_bib0260
  article-title: The Arg753GLn polymorphism of the human toll-like receptor 2 gene in tuberculosis disease
  publication-title: Eur Respir J
  doi: 10.1183/09031936.03.00061703
– volume: 26
  start-page: 241
  year: 2011
  ident: 10.1016/j.medici.2018.01.001_bib0310
  article-title: Folate supplementation, MTHFR gene polymorphism and neural tube defects: a community based case control study in North India
  publication-title: Metab Brain Dis
  doi: 10.1007/s11011-011-9256-8
– volume: 105
  start-page: 149
  year: 2014
  ident: 10.1016/j.medici.2018.01.001_bib0250
  article-title: Perinatal outcomes of pregnancies complicated by maternal depression with or without
  publication-title: Neonatology
  doi: 10.1159/000356774
– volume: 95
  start-page: 157
  year: 2016
  ident: 10.1016/j.medici.2018.01.001_bib0205
  article-title: Association of methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with preterm delivery and placental abruption: a systematic review and meta-analysis
  publication-title: AOGS
  doi: 10.1111/aogs.12789
– volume: 195
  year: 2006
  ident: 10.1016/j.medici.2018.01.001_bib0290
  article-title: Polymorphisms in folate metabolizing genes and risk for spontaneous preterm and small-for-gestational age birth
  publication-title: Am J Obstet Gynecol
  doi: 10.1016/j.ajog.2006.07.024
– volume: 88
  start-page: 31
  year: 2010
  ident: 10.1016/j.medici.2018.01.001_bib0185
  article-title: The worldwide incidence of preterm birth: a systematic review of maternal mortality and morbidity
  publication-title: Bull World Health Organ
  doi: 10.2471/BLT.08.062554
– volume: 616
  start-page: 26
  year: 2016
  ident: 10.1016/j.medici.2018.01.001_bib0305
  article-title: Association of the MTHFR rs1801131 and rs1801133 variants in sporadic Parkinson's disease patients
  publication-title: Neurosci Lett
  doi: 10.1016/j.neulet.2016.01.031
– volume: 107
  start-page: 162
  year: 2002
  ident: 10.1016/j.medici.2018.01.001_bib0270
  article-title: Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A
  publication-title: Am J Epidemiol
– volume: 8
  start-page: 7397
  year: 2015
  ident: 10.1016/j.medici.2018.01.001_bib0210
  article-title: MTHFR genetic polymorphism increases the risk of preterm delivery
  publication-title: Int J Clin Exp Pathol
– volume: 9
  start-page: 379
  year: 2012
  ident: 10.1016/j.medici.2018.01.001_bib0180
  article-title: National, regional, and worldwide estimates of preterm birth rates in the year 2010 with timetrends since 1990 for selected countries: a systematic analysis and implication
  publication-title: Lancet
– volume: 39
  start-page: 689
  year: 2017
  ident: 10.1016/j.medici.2018.01.001_bib0235
  article-title: Methylenetetrahydrofolate reductase, MTHFR, polymorphisms and prediposition to different multifactorial disorders
  publication-title: Genes Genomics
  doi: 10.1007/s13258-017-0552-5
– volume: 159
  start-page: 423
  year: 2004
  ident: 10.1016/j.medici.2018.01.001_bib0300
  article-title: Polymorphisms in genes involved in folate metabolism and colorectal neoplasia: a HuGE review
  publication-title: Am J Epidemiol
  doi: 10.1093/aje/kwh066
– volume: 3
  start-page: 74
  year: 2010
  ident: 10.1016/j.medici.2018.01.001_bib0265
  article-title: Polymorphisms of 5,10-methylenetetrahydrofolate reductase and thymidylate synthase in squamous cell carcinoma and basal cell carcinoma of the skin
  publication-title: Mol Med Rep
– volume: 34
  start-page: 894
  year: 2013
  ident: 10.1016/j.medici.2018.01.001_bib0280
  article-title: Relationship of plasma homocysteine levels, folate levels and MTHFR gene polymorphisms with premature delivery
  publication-title: J Sun Yat-sen Univ (Med Sci)
SSID ssj0032572
Score 2.1359892
Snippet The MTHFR gene encodes the methylenetetrahydrofolate reductase known to be involved in the homocysteine–methionine pathway. It has been reported that the...
The MTHFR gene encodes the methylenetetrahydrofolate reductase known to be involved in the homocysteine-methionine pathway. It has been reported that the...
Background and objective: The MTHFR gene encodes the methylenetetrahydrofolate reductase known to be involved in the homocysteine–methionine pathway. It has...
SourceID doaj
proquest
pubmed
crossref
elsevier
SourceType Open Website
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 380
SubjectTerms Genetic association
Korean women
MTHFR
Polymorphism
Preterm birth
Title Genetic variations of MTHFR gene and their association with preterm birth in Korean women
URI https://dx.doi.org/10.1016/j.medici.2018.01.001
https://www.ncbi.nlm.nih.gov/pubmed/29428336
https://www.proquest.com/docview/2001405659
https://doaj.org/article/e1949a360931448f8be046ab9a53edec
Volume 53
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV07T8MwELZQB8SCeFNeMhJrRBLHj4yAqCpQGVArlclyHEcqQgkqLb-fOzspMKAujEmcxDpfzt898h0hVxJ85NRwHlnkv8xUpiKT8iIyqkzzSqRS-XjH6EkMJ9nDlE9_tPrCmrBADxwEd-3Ay84NE-B5A_ZXlSocuHSmyA1nrnQWrW-cx50zFWwwA0UMeU6wMkLE0-6nOV_ZFbLWWNalPGVn2xCm25Q8d_-vvekv7On3oMEO2W7BI70Jk94lG67eI5ujNj2-T16QRBqu0U_wgEMojjYVHY2Hg2cKmuKoqUvqcwPUfK8LxWAsxcpDMNO0mM3haFbTxwYAJVxEjoYDMhncj--GUds7IbKZzBaR5ZVkHNAWV04wY3NRKpYkQlSAOAAjMYFUgEkirZXSglhTbPbirEgLUyBp3iHp1U3tjgm1RgAo4-CnlDIzJi-YVUgiD1ufSZyRfcI64WnbEotjf4s33VWQveogco0i13GChXR9Eq3ueg_EGmvG3-K6rMYiLbY_AcqiW2XR65SlT2S3qrpFGAE5wKNma15_2SmBhg8Qsyqmds3yA_t4gpMKuDjvk6OgHatJpjny2TFx8h-TPyVbKWIKH_85I73FfOnOAREtiguv_F-w3gMU
linkProvider Directory of Open Access Journals
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Genetic+variations+of+MTHFR+gene+and+their+association+with+preterm-birth+in+Korean+women&rft.jtitle=Medicina+%28Kaunas%2C+Lithuania%29&rft.au=Hwang%2C+In+Wook&rft.au=Kang%2C+Yun+Dan&rft.au=Kwon%2C+Bit+Na&rft.au=Hong%2C+Jun+Ho&rft.date=2017-01-01&rft.eissn=1648-9144&rft_id=info:doi/10.1016%2Fj.medici.2018.01.001&rft_id=info%3Apmid%2F29428336&rft.externalDocID=29428336
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1010-660X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1010-660X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1010-660X&client=summon