Preterm births strongly related to Vitamin D, Vitamin D Receptor, Iodine, Omega-3, etc
Vitamin D Life
Preterm Births reduced by Omega-3, Zinc, and Vitamin D – Aug 2019
see Vitamin D Life Preterm Births reduced by Omega-3, Zinc, and Vitamin D – Aug 2019
Preterm Births decreased by Omega-3 (analysis of 184 countries) – April 2019
see Vitamin D Life Preterm Births decreased by Omega-3 (analysis of 184 countries) – April 2019
VDR, spontaneous preterm birth and gestational diabetes– Feb 2018
Vitamin D receptor (VDR) polymorphisms are associated to spontaneous preterm birth and maternal aspects
Gene, Volume 642, 5 February 2018, Pages 58–63, https://doi.org/10.1016/j.gene.2017.10.087
N. Javorskia, b, C.A.D. Limaa, b, L.V.C. Silvac, S. Crovellaa, b, J. de Azêvedo Silvaa, b, ,
Highlights
This is a new report relating polymorphisms within VDR gene and prematurity's outcomes.
Herein we correlate clinical characteristics and spontaneous preterm birth, according to the maternal VDR genotype.
Detection of direct relationship between VDR recessive genotype and specific clinical aspects in women with SPTB.
Preterm birth (PTB) is featured by less than 37 weeks of gestational age or fewer than 259 days since the first day from the last menstrual period. Complications of PTB are the major cause of neonatal deaths, several factors are linked to PTB increased risk including immunological and genetics. Vitamin D plays an important role in immune response modulation and its action occurs through the vitamin D receptor (VDR), which recently has been described as overexpressed in human placenta during the pregnancy. Herein we assessed two single nucleotide polymorphisms (SNPs) FokI (rs2228570 A > G) and Cdx-2 (rs11568820 T > C), within VDR, using TaqMan fluorogenic probes, and differential susceptibility to SPTB.
We assessed 104 pregnant women with SPTB and 85 women with normal birth in a Northeastern Brazilian population. Statistically significant differences for both SNPs where found when comparing allele and genotype frequencies in both groups: the T allele for rs2228570 and A allele for rs11568820 were significantly more frequent in SPTB group than in normal birth group (p = 0.000013 and p = 0.00466, respectively).
The rs11568820 A/A genotype was associated to clinical/demographic variables such as:
premature birth (p = 0.007),
neonate weight (p = 0.039),
presence of infection during pregnancy (p = 0.011) and
premature birth among multiparous (p = 0.015).
The rs2228570 T/T genotype associated with
gestational diabetes mellitus (p = 0.044) and
chorioamnionitis during pregnancy (p = 0.043).
In conclusion our findings indicate an association between polymorphisms FokI and Cdx-2 within VDR gene and SPTB, suggesting their involvement in the triggering of these syndromes.
Abbreviations
PTB, Preterm birth; SPTB, Spontaneous preterm birth; PROM, Premature rupture of membranes; GDM, Gestational diabetes mellitus; VDR, Vitamin D receptor; TNF, Tumor necrosis factor; IL, interleukin; OR, Odds ratio; CI, Confidence interval
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Preterm Birth 3.3X as likely if poor VDR – Aug 2016
Relationship between vitamin D receptor gene polymorphism and preterm birth. [Article in Chinese]
Nan Fang Yi Ke Da Xue Xue Bao. 2016 Aug 20;36(9):1276-1280.
Cai W1, Shen XY, Zhu BP, Pan SL.
OBJECTIVE: To explore the relationship between vitamin D receptor (VDR) gene polymorphisms at Fok I site and the risk of preterm birth for potential intervention of of preterm birth or threatened premature delivery.
METHODS: Fifty-seven women with preterm birth and 84 with full-term birth were included in this analysis. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was performed to identify VDR gene Fok I genotypes.
RESULTS: No significant difference was found in age, D-dimer (DDI), fibrinogen (Fg), serum calcium (Ca2+), leukocyte count or glycosylated hemoglobin (HbA1c) level between the women in the preterm and full-term birth groups (P>0.05). The two groups differed significantly in the distribution of VDR gene Fok I site genotypes and allele frequency of F/F (P<0.05).The frequency of FF genotype was significantly higher in the preterm group than in the full-term group. Compared with Ff and ff genotypes, FF genotype was associated with an increased risk of preterm delivery (χ2=9.701, P=9.701, OR=3.320 , 95% CI [1.560, 7.066]). In the preterm group, the maternal age, DDI, Fg, serum Ca2+, leukocyte count or HbA1c did not differ significantly between the genotypes (P>0.05).
CONCLUSION: VDR gene Fok I site genotypes are related with preterm birth, and the FF genotype may serve as a potential risk factor for preterm birth.
PMID: 27687664
Preterm birth 34 X more likely if have worst VDR combination - Dec 2016
Influence of Apa1 (rs7975232), Taq1 (rs731236) and Bsm1 (rs154410) polymorphisms of vitamin D receptor on preterm birth risk in the Polish population.
Ginekol Pol. 2016;87(11):763-768. doi: 10.5603/GP.2016.0084.
Baczyńska-Strzecha M1, Kalinka J.
1Department of Perinatology, 1st Chair of Obstetrics and Gynecology, Medical University in Lodz, Poland. [email protected].
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OBJECTIVES:
Vitamin D receptor (VDR) is expressed in the placenta and tissues related to the immune system occurrence of various variants of VDR may modify the effects of vitamin D on pregnancy. The aim of this study was to evaluate the association between the parturients' Apa1, Taq1, and Bsm1 polymorphisms of the VDR and their combinations and the risk of preterm birth in the Polish population.
MATERIAL AND METHODS:
Determination of polymorphism for VDR was assayed using the RT-PCR method. 199 Caucasian women at childbirth were qualified:100 patients who had a spontaneous preterm birth and 99 patients who had a term birth.
RESULTS:
Three separate genotypes of the Apa1, Taq1, and Bsm1 polymorphisms were detected. No significant differences in the frequency of particular genotypes in the compared groups were found. Some of the genotype combinations were significantly more frequent in the preterm group - the bb/AA/TT genotype (28.0% vs. 10.1%; p = 0.0013) and the BB/aa/tt genotype (14.0% vs. 4.04% p = 0.0277). The Bb/AA/Tt and the BB/Aa/tt genotypes were found only in the control group (16.1% and 7.0% of patients, respectively). The bb/aa/TT was significantly more frequent in the control group (2.0% vs. 11.1%; p = 0,0207).
Two genotype combinations reduced the risk of preterm birth - the
Bb/AA/Tt genotype by 94% (OR = 0.43, 95% CI: 0.002-0.885, p = 0.041) and the
BB/Aa/tt genotype by 98% ( OR = 0.029 , 95% CI: 0.001-0.838, p = 0.039).
CONCLUSIONS:
Our result suggests that there may be a relationship between certain VDR genotype combinations and the risk of preterm birth. Further research is needed in order to substantiate this finding.
Preterm Birth twice as likely if poor VDR – Sept 2017
VITAMIN D RECEPTOR (VDR) GENE POLYMORPHISM AND MATERNAL VITAMIN D DEFICIENCY IN INDIAN WOMEN WITH PRETERM BIRTH (PTB)
Asian Journal of Pharmaceutical and Clinical Research / academic sciences, Vol 10, Issue 9, 2017
HITESH V PATEL1*, NAYANA H PATEL2, NILOFAR R SODAGAR2
department of Biochemistry, Shri A. N. Patel PG Institute, Sardar Patel University, Anand - 388 001, Gujarat, India. department of Gynecology and Obstetrics, Akanksha Hospital & Research Institute, Anand - 387 310, Gujarat, India. Email: [email protected]
Objective: Preterm birth (PTB) is the leading cause of high infant mortality and long-term disability in young children worldwide. Array of adverse maternal and fetal outcomes linked with vitamin D level and its associated vitamin D receptor (VDR) gene. We undertook this study to investigate the association between VDR gene polymorphism with vitamin D deficiency and PTB in West Indian pregnant women.
Methods: A total of 72 women with PTB and 138 healthy mothers with uncomplicated normal delivery were selected from different regions of Gujarat, India. FokI and TaqI single nucleotide polymorphism (SNP) of VDR gene determined by polymerase chain reaction and restriction fragment length polymorphism. Vitamin D level was determined using enzyme-linked immunosorbent assay.
Result: ff genotype (29.17% vs. 10.87%, p=0.002) and f allele (49.31% vs. 35.51%, p=0.006) frequency distributions of VDR FokI showed significantly ( odds ratio=0.566 , 95% confidence interval=0.368-0.870, p=0.006) higher in women with preterm delivery than in control full term group. Genotype frequency of VDR TaqI showed no significant difference between preterm group and control.
Conclusion: These results confirmed that women carrying ff genotype of FokI gene had significantly higher risk for vitamin D deficiency which enhances the risk of prematurity than women carrying FF genotype in West Indian women.
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