Abstract:Background
Genetic factors are important considerations in the etiology of preeclampsia and gestational hypertension. Several previous studies have shown an association of Vitamin D receptor (VDR) gene polymorphisms with hypertension in pregnancy. However, the number of studies is still very limited and the results differ from one another.
Aim of the study
This study aimed to analyze the polymorphisms of rs2228570 and rs731236 of the VDR gene in su… Show more
“…In the present study, approximately 6 (67%) studies used PCR-RFLP (26, 27,42,44,45,47). All studies that utilized PCR-RFLP demonstrated an association with FokI and were reported from Asian populations (27,42,44). In contrast, one study reported an association with the ApaI variant (45).…”
Section: Association Of Vdr Gene Variants With Hdp Detected Using Dif...mentioning
confidence: 64%
“…According to our based on population, 4 (44%) studies that showed an association with the FokI variant were reported in Asian populations (27,42,44,46). However, one study of Caucasians in Italy reported an association with the combined variant of FokI and BsmI (43).…”
Section: Association Of Vdr Gene Variants With Hdp In the Studied Pop...mentioning
confidence: 92%
“…Approximately 56% of the included studies reported an association between the FokI variant and an increased risk of HDP (27,(42)(43)(44)46). According to a study of Madura pregnant women in Indonesia, the FokI TT genotype of the VDR variant is linked with a 3-fold increased vulnerability to developing GH (27).…”
Section: Association Analysis Of Vdr Variants With Hdp Among Populationsmentioning
confidence: 99%
“…Numerous studies have examined the association of BsmI variants and an increased risk of GH; however, ndings have been inconsistent across different authors and ethnic groups. Some studies found no signi cant link between the BsmI variant and increased GH risk (27,42,(44)(45)(46), while others showed a correlation between speci c genotypes (Bb and bb) and hypertensive disorders during pregnancy (26,43). In a Polish study, the BsmI AA genotype was more prevalent in mothers with PE and was related to a 2-fold risk of preeclampsia development (26).…”
Section: Association Analysis Of Vdr Variants With Hdp Among Populationsmentioning
confidence: 99%
“…The VDR variants sequences and other background information are shown (Table 1). Numerous studies have been carried out to investigate the role of VDR genetic polymorphisms in the pathogenesis of pregnancy complications, including GH, PE, GDM, preterm delivery and miscarriages (17,(24)(25)(26)(27)(28)(29). In addition to genetic variations in the VDR, recent evidence has suggested that vitamin D de cit is associated with reduced endothelial VDR expression, resulting in inadequate vitamin D action and more severe pregnancy complications, such as hypertensive disorders (11).…”
Introduction:
Hypertensive disorders of pregnancy constitute the major cause of maternal morbidity and mortality. Genetic variation involving VDR gene variants was thought to play a significant role in aetiopathogenesis of HDP. Vitamin D receptor (VDR) gene polymorphisms are thought to be implicated in the development of hypertensive disorders of pregnancy (HDP). However, the association of the variants with HDP is inconsistently reported. The study aims to review the laboratory protocols of VDR variant detection and association with HDP.
Methods
This study involved one or more of the major VDR gene variants (FokI, BsmI, ApaI, and TaqI) in HDP. The Web of Science, PubMed, Scopus, MEDLINE and CINAHL databases were searched for articles. Preferred Reporting Items for Systematic Review and Meta-analysis (PRISMA) was used. The study was registered in the PROSPERO database (registration number CRD42022362561).
Results
Our analysis of VDR variant detection protocols revealed that approximately 6 (67%) studies used polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP), of which 3 (33%) reported a significant association with the FokI variant. Two (22%) of the studies used TaqMan PCR and found an association with the FokI variant. Only 1 (11%) study utilized allele-specific PCR (AS-PCR) to genotype the ApaI variant. Based on the analysis of the variants with populations, 4 studies (44%) reported an association with the FokI variant in Asians. Two studies (22%) reported that the BsmI variant is common among Caucasians.
Conclusions
The detection protocols evaluated were found to be sensitive in detecting some variants in certain populations but not in others, however, the variants were found to be population-specific. Our findings could potentially be useful in stimulating the discovery of distinct biomarkers specific to various populations and could as well prompt the personalised management of hypertension in pregnancy.
“…In the present study, approximately 6 (67%) studies used PCR-RFLP (26, 27,42,44,45,47). All studies that utilized PCR-RFLP demonstrated an association with FokI and were reported from Asian populations (27,42,44). In contrast, one study reported an association with the ApaI variant (45).…”
Section: Association Of Vdr Gene Variants With Hdp Detected Using Dif...mentioning
confidence: 64%
“…According to our based on population, 4 (44%) studies that showed an association with the FokI variant were reported in Asian populations (27,42,44,46). However, one study of Caucasians in Italy reported an association with the combined variant of FokI and BsmI (43).…”
Section: Association Of Vdr Gene Variants With Hdp In the Studied Pop...mentioning
confidence: 92%
“…Approximately 56% of the included studies reported an association between the FokI variant and an increased risk of HDP (27,(42)(43)(44)46). According to a study of Madura pregnant women in Indonesia, the FokI TT genotype of the VDR variant is linked with a 3-fold increased vulnerability to developing GH (27).…”
Section: Association Analysis Of Vdr Variants With Hdp Among Populationsmentioning
confidence: 99%
“…Numerous studies have examined the association of BsmI variants and an increased risk of GH; however, ndings have been inconsistent across different authors and ethnic groups. Some studies found no signi cant link between the BsmI variant and increased GH risk (27,42,(44)(45)(46), while others showed a correlation between speci c genotypes (Bb and bb) and hypertensive disorders during pregnancy (26,43). In a Polish study, the BsmI AA genotype was more prevalent in mothers with PE and was related to a 2-fold risk of preeclampsia development (26).…”
Section: Association Analysis Of Vdr Variants With Hdp Among Populationsmentioning
confidence: 99%
“…The VDR variants sequences and other background information are shown (Table 1). Numerous studies have been carried out to investigate the role of VDR genetic polymorphisms in the pathogenesis of pregnancy complications, including GH, PE, GDM, preterm delivery and miscarriages (17,(24)(25)(26)(27)(28)(29). In addition to genetic variations in the VDR, recent evidence has suggested that vitamin D de cit is associated with reduced endothelial VDR expression, resulting in inadequate vitamin D action and more severe pregnancy complications, such as hypertensive disorders (11).…”
Introduction:
Hypertensive disorders of pregnancy constitute the major cause of maternal morbidity and mortality. Genetic variation involving VDR gene variants was thought to play a significant role in aetiopathogenesis of HDP. Vitamin D receptor (VDR) gene polymorphisms are thought to be implicated in the development of hypertensive disorders of pregnancy (HDP). However, the association of the variants with HDP is inconsistently reported. The study aims to review the laboratory protocols of VDR variant detection and association with HDP.
Methods
This study involved one or more of the major VDR gene variants (FokI, BsmI, ApaI, and TaqI) in HDP. The Web of Science, PubMed, Scopus, MEDLINE and CINAHL databases were searched for articles. Preferred Reporting Items for Systematic Review and Meta-analysis (PRISMA) was used. The study was registered in the PROSPERO database (registration number CRD42022362561).
Results
Our analysis of VDR variant detection protocols revealed that approximately 6 (67%) studies used polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP), of which 3 (33%) reported a significant association with the FokI variant. Two (22%) of the studies used TaqMan PCR and found an association with the FokI variant. Only 1 (11%) study utilized allele-specific PCR (AS-PCR) to genotype the ApaI variant. Based on the analysis of the variants with populations, 4 studies (44%) reported an association with the FokI variant in Asians. Two studies (22%) reported that the BsmI variant is common among Caucasians.
Conclusions
The detection protocols evaluated were found to be sensitive in detecting some variants in certain populations but not in others, however, the variants were found to be population-specific. Our findings could potentially be useful in stimulating the discovery of distinct biomarkers specific to various populations and could as well prompt the personalised management of hypertension in pregnancy.
Background
Hypertensive disorders of pregnancy (HDP) are currently one of the major causes of pregnancy-related maternal and fetal morbidity and mortality worldwide. Recent studies provide evidence that maternal Vitamin D receptor (VDR) gene polymorphisms probably play a key role by affecting the biological function of vitamin D in some adverse pregnancy outcomes, while the relationship between the VDR gene polymorphisms and the risk of HDP remains controversial in current studies. This systematic review and meta-analysis aimed to comprehensively evaluate the association of the VDR gene polymorphisms with HDP susceptibility.
Methods
This meta-analysis follows the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement and a protocol has been registered in the PROSPERO (ID: CRD42022344383) before commencing this review. PubMed, Web of Science, Embase, and the Cochrane Library databases were searched until January 21, 2023. Case-control and cohort studies that reported the association of the VDR gene polymorphisms with HDP were included. The quality of the included studies was assessed using the Newcastle-Ottawa Scale (NOS) for non-randomized studies. The odds ratios (ORs) with corresponding 95% confidence intervals (CIs) of the five models (allele model, dominant model, recessive model, homozygous model, heterozygous model) were pooled respectively, and subgroup analysis was performed based on ethnicity.
Results
A total of ten studies were included. The VDR gene ApaI polymorphism was associated with HDP susceptibility in the dominant model (OR: 1.38; 95% CI [1.07–1.79]; P = 0.014) and the heterozygote model (OR: 1.48; 95% CI [1.12–1.95]; P = 0.006). In subgroup analysis, the heterozygote model (OR: 2.06; 95% CI [1.21–3.52]; P = 0.008) of the ApaI polymorphism was associated with HDP in Asians, but not in Caucasians.
Conclusion
The VDR gene ApaI polymorphism may be associated with HDP susceptibility. Insufficient evidence to support the existence of ethnic differences in this association.
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