Association of Bach1 Gene Polymorphisms with Susceptibility to Bronchopulmonary Dysplasia in Preterm Infants

<b>Background:</b> BTB and CNC homology 1 (<i>Bach1</i>) are transcriptional regulators involved in the oxidative response and inflammation. Although its biological functions are well characterized, the clinical impact of <i>Bach1</i> gene polymorphisms (rs2300301, rs1153285, and rs2070401) on respiratory outcomes in preterm infants remains unclear. <b>Methods:</b> This multicenter study included 212 Japanese preterm infants born at <32 weeks of gestation with birth weights <1250 g. Three <i>Bach1</i> single-nucleotide polymorphisms (SNPs; rs2300301, rs1153285, and rs2070401) were genotyped using TaqMan polymerase chain reaction (PCR). The requirements for home oxygen therapy (HOT) were compared across genotypes. Logistic regression analyses were performed after adjusting for the gestational age, sex, birth weight, and histological chorioamnionitis status. <b>Results:</b> Infants requiring HOT had a significantly lower gestational age (26 ± 1.7 weeks vs. 27 ± 2.2 weeks, <i>p</i> = 0.015) and lower birth weight (774 ± 235 g vs. 818 ± 233 g, <i>p</i> = 0.043) than those who did not. Histological chorioamnionitis was more prevalent in the HOT group (<i>p</i> = 0.022). rs2300301 was associated with HOT in univariate analysis (OR = 1.78, 95% CI: 1.20-2.04, <i>p</i> = 0.015). However, this association did not remain statistically significant after adjustment for gestational age, sex, birth weight, and histological chorioamnionitis (OR = 2.48, 95% CI: 0.90-6.80, <i>p</i> = 0.079). The rs1153285 and rs2070401 SNPs were not significantly associated with HOT expression. <b>Conclusions:</b> Our findings suggest a potential association between the <i>Bach1</i> rs2300301 polymorphism and prolonged oxygen requirement in preterm infants. Although the adjusted analysis did not confirm the statistical significance, this SNP may serve as a candidate genetic marker for respiratory morbidity. Further studies are required to validate these findings.

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Journal
Biomedicines
Published
2025-12-21
DOI
https://doi.org/10.3390/biomedicines14010017
Citations
1
Primary Topic
Neonatal Respiratory Health Research
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article
Field-Weighted Citation Impact
1.52
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article

Association of Bach1 Gene Polymorphisms with Susceptibility to Bronchopulmonary Dysplasia in Preterm Infants

Hirokazu Arai, Mitsuhiro Haga, Nobuhiko Nagano, Shunsuke Araki et al.
1 citations
Biomedicines
Neonatal Respiratory Health Research
1.52
article

Association of Bach1 Gene Polymorphisms with Susceptibility to Bronchopulmonary Dysplasia in Preterm Infants

Hirokazu Arai, Mitsuhiro Haga, Nobuhiko Nagano, Shunsuke Araki, Ayumi Sasaki, Ayaka Iwatani, Eri Nishimura, Masato Ito, Yoshihiro Onouchi, Fumihiko Namba, Asami Konishi, Atsuko Noguchi, Satomi Sakuraba, Shutaro Suga
article en
1 citations

Abstract

<b>Background:</b> BTB and CNC homology 1 (<i>Bach1</i>) are transcriptional regulators involved in the oxidative response and inflammation. Although its biological functions are well characterized, the clinical impact of <i>Bach1</i> gene polymorphisms (rs2300301, rs1153285, and rs2070401) on respiratory outcomes in preterm infants remains unclear. <b>Methods:</b> This multicenter study included 212 Japanese preterm infants born at <32 weeks of gestation with birth weights <1250 g. Three <i>Bach1</i> single-nucleotide polymorphisms (SNPs; rs2300301, rs1153285, and rs2070401) were genotyped using TaqMan polymerase chain reaction (PCR). The requirements for home oxygen therapy (HOT) were compared across genotypes. Logistic regression analyses were performed after adjusting for the gestational age, sex, birth weight, and histological chorioamnionitis status. <b>Results:</b> Infants requiring HOT had a significantly lower gestational age (26 ± 1.7 weeks vs. 27 ± 2.2 weeks, <i>p</i> = 0.015) and lower birth weight (774 ± 235 g vs. 818 ± 233 g, <i>p</i> = 0.043) than those who did not. Histological chorioamnionitis was more prevalent in the HOT group (<i>p</i> = 0.022). rs2300301 was associated with HOT in univariate analysis (OR = 1.78, 95% CI: 1.20-2.04, <i>p</i> = 0.015). However, this association did not remain statistically significant after adjustment for gestational age, sex, birth weight, and histological chorioamnionitis (OR = 2.48, 95% CI: 0.90-6.80, <i>p</i> = 0.079). The rs1153285 and rs2070401 SNPs were not significantly associated with HOT expression. <b>Conclusions:</b> Our findings suggest a potential association between the <i>Bach1</i> rs2300301 polymorphism and prolonged oxygen requirement in preterm infants. Although the adjusted analysis did not confirm the statistical significance, this SNP may serve as a candidate genetic marker for respiratory morbidity. Further studies are required to validate these findings.

BiomedicinesVol. 14(1)
Nihon University (JP), Chiba University (JP), University of Occupational and Environmental Health Japan (JP), Akita University (JP), Akita Red Cross Hospital (JP), Social Insurance Saitama Chuo Hospital (JP), Saitama Medical University (JP)
Good health and well-being
Openalex Percentile: Top 12%
Neonatal Respiratory Health Research
1.52
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