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婴儿出生结局与通过胞质分裂阻滞微核细胞分析法测量的DNA损伤生物标志物相关:DADHI研究。

Infant birth outcomes are associated with DNA damage biomarkers as measured by the cytokinesis block micronucleus cytome assay: the DADHI study.

作者信息

Dass Singh Mansi, Thomas Philip, Hor Maryam, Almond Theodora, Owens Julie, Hague William, Fenech Michael

机构信息

Commonwealth Scientific and Industrial Research Organization (CSIRO) Health & Biosecurity, Personalised Nutrition and Healthy Ageing, Adelaide, South Australia 5000, Australia.

Discipline of Obstetrics and Gynecology, School of Medicine, Faculty of Health Sciences, The University of Adelaide, Adelaide 5000, South Australia, Australia and.

出版信息

Mutagenesis. 2017 May 1;32(3):355-370. doi: 10.1093/mutage/gex001.

Abstract

Accumulation of DNA damage in the first 1000 days may increase risk of accelerated ageing and degenerative diseases in adult life such as cancers. The extent of DNA damage in infants and the correlation of maternal factors during pregnancy with neonate birth outcomes and DNA damage is not known in infants born in Australia. Therefore, we performed a prospective cohort study to collect data on DNA damage in lymphocytes of Australian infants (aged 0, 3 and 6 months), using the cytokinesis block micronucleus cytome (CBMN-Cyt) assay. The study also explored correlation of CBMN-Cyt biomarkers with infant birth outcomes and maternal anthropometric and lifestyle variables. Peripheral blood lymphocytes were isolated from the infants at birth (cord blood) (n = 82), 3 months (n = 64) and 6 months (n = 53) after birth. DNA damage biomarkers measured ex vivo in binucleated lymphocytes (BNC) included: micronuclei (MN), nucleoplasmic bridges (NPB) and nuclear buds (NBUD). Apoptotic and necrotic lymphocytes were also scored and nuclear division index (NDI) was measured using the frequency of mono-, bi- and multinucleated lymphocyte. MN and NBUD were also scored in mononucleated lymphocytes (MNC). The mean (± SD) frequency of MN, NPB and NBUD in BNCs at birth was 2.0 (± 1.2), 5.8 (± 3.7) and 11.1 (± 5.7) per 1000 BNC, respectively, and tended to decrease significantly at 3 months (P < 0.01, P < 0.0001, P < 0.001, respectively) and 6 months (P < 0.05, P < 0.0001, P < 0.0001, respectively) after birth relative to cord blood when compared with the same cohort of infants (n = 48 at birth, 48 at 3 months and 39 at 6 months). None of the CBMN cytome biomarkers measured at birth was associated with maternal smoking status, alcohol and folic acid intake during pregnancy. The mean gestation age correlated positively with MN (r = 0.38, P = 0.006), NPB (r = 0.30, P = 0.03) and negatively with NDI (r = -0.29, P = 0.03). Infant birth weight associated positively with MN, NPB and NBUD in cord blood (r = 0.24, P = 0.08; r = 0.32, P = 0.02; r = 0.28, P = 0.04, respectively), birth length associated positively with NPB (r = 0.32, P = 0.02) and NBUD (r = 0.27, P = 0.04) while head circumference associated negatively with apoptotic cells (r = -0.27, P = 0.06). APGAR score at 1 and 5 min after birth associated positively with NDI at birth (r = 0.3, P = 0.05, r = 0.28, P = 0.06, respectively). Mother's weight and body mass index (BMI) recorded at the time of recruitment associated positively with NPB (r = 0.38, P = 0.006, r = 0.32, P = 0.02, respectively) and negatively with APGAR score at 5 min (r = -0.25, P = 0.07). The significant positive associations of infant birth weight and length and maternal BMI with CBMN-Cyt biomarkers suggest the possibility of a genotoxic effect of metabolic processes that promote excessive growth and high BMI.

摘要

出生后头1000天内DNA损伤的积累可能会增加成年后加速衰老和患退行性疾病(如癌症)的风险。在澳大利亚出生的婴儿中,婴儿期DNA损伤的程度以及孕期母亲因素与新生儿出生结局和DNA损伤之间的相关性尚不清楚。因此,我们进行了一项前瞻性队列研究,采用胞质分裂阻滞微核细胞组学(CBMN-Cyt)检测方法,收集澳大利亚婴儿(0、3和6个月大)淋巴细胞中DNA损伤的数据。该研究还探讨了CBMN-Cyt生物标志物与婴儿出生结局以及母亲人体测量和生活方式变量之间的相关性。在婴儿出生时(脐带血)(n = 82)、出生后3个月(n = 64)和6个月(n = 53)采集外周血淋巴细胞。在双核淋巴细胞(BNC)中离体测量的DNA损伤生物标志物包括:微核(MN)、核质桥(NPB)和核芽(NBUD)。还对凋亡和坏死淋巴细胞进行了评分,并使用单核、双核和多核淋巴细胞的频率测量核分裂指数(NDI)。在单核淋巴细胞(MNC)中也对MN和NBUD进行了评分。出生时BNC中MN、NPB和NBUD的平均(±标准差)频率分别为每1000个BNC中2.0(±1.2)、5.8(±3.7)和11.1(±5.7),与同一队列婴儿(出生时n = 48,3个月时n = 48,6个月时n = 39)的脐带血相比,在出生后3个月(分别为P < 0.01、P < 0.0001、P < 0.001)和6个月(分别为P < 0.05、P < 0.0001、P < 0.0001)时显著下降。出生时测量的CBMN细胞组学生物标志物均与母亲孕期吸烟状况、酒精和叶酸摄入量无关。平均胎龄与MN呈正相关(r = 0.38,P = 0.006)、与NPB呈正相关(r = 0.30,P = 0.03),与NDI呈负相关(r = -0.29,P = 0.03)。婴儿出生体重与脐带血中的MN、NPB和NBUD呈正相关(分别为r = 0.24,P = 0.08;r = 0.32,P = 0.02;r = 0.28,P = 0.04),出生身长与NPB呈正相关(r = 0.32,P = 0.02)、与NBUD呈正相关(r = 0.27,P = 0.04),而头围与凋亡细胞呈负相关(r = -0.27,P = 0.06)。出生后1分钟和5分钟时的阿氏评分与出生时的NDI呈正相关(分别为r = 0.3,P = 0.05;r = 0.28,P = 0.06)。招募时记录的母亲体重和体重指数(BMI)与NPB呈正相关(分别为r = 0.38,P = 0.006;r = 0.32,P = 0.02),与出生后5分钟时的阿氏评分呈负相关(r = -0.25,P = 0.07)。婴儿出生体重、身长和母亲BMI与CBMN-Cyt生物标志物之间的显著正相关表明,促进过度生长和高BMI的代谢过程可能具有遗传毒性作用。

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