{"title":"DNA甲基化介导中国单卵双胞胎体重指数与血压的关系","authors":"Jie Yao, Feng Ning, Weijing Wang, Dongfeng Zhang","doi":"10.1017/thg.2024.3","DOIUrl":null,"url":null,"abstract":"<p><p>Obesity is an established risk factor for hypertension, but the mechanisms are only partially understood. We examined whether body mass index (BMI)-related DNA methylation (DNAm) variation would mediate the association of BMI with blood pressure (BP). We first conducted a genomewide DNA methylation analysis in monozygotic twin pairs to detect BMI-related DNAm variation and then evaluated the mediating effect of DNAm on the relationship between BMI and BP levels using the causal inference test (CIT) method and mediation analysis. Ontology enrichment analysis was performed for CpGs using the GREAT tool. A total of 60 twin pairs for BMI and systolic blood pressure (SBP) and 58 twin pairs for BMI and diastolic blood pressure (DBP) were included. BMI was positively associated with SBP (β = 1.86, <i>p</i> = .0004). The association between BMI and DNAm of 85 CpGs reached <i>p</i> < 1×10<sup>-4</sup> level. Eleven BMI-related differentially methylated regions (DMRs) within <i>LNCPRESS1</i>, <i>OGDHL</i>, <i>RNU1-44P</i>, <i>NPHS1</i>, <i>ECEL1P2</i>, <i>LLGL2</i>, <i>RNY4P15</i>, <i>MOGAT3</i>, <i>PHACTR3</i>, and <i>BAI2</i> were found. Of the 85 CpGs, 9 mapped to <i>C10orf71-AS1</i>, <i>NDUFB5P1</i>, <i>KRT80</i>, <i>BAI2</i>, <i>ABCA2</i>, <i>PEX11G</i> and <i>FGF4</i> were significantly associated with SBP levels. Of the 9 CpGs, 2 within <i>ABCA2</i> negatively mediated the association between BMI and SBP, with a mediating effect of -0.24 (95% CI [-0.65, -0.01]). BMI was also positively associated with DBP (β = 0.60, <i>p</i> = .0495). The association between BMI and DNAm of 193 CpGs reached <i>p</i> < 1×10<sup>-4</sup> level. Twenty-five BMI-related DMRs within <i>OGDHL</i>, <i>POU4F2</i>, <i>ECEL1P2</i>, <i>TTC6</i>, <i>SMPD4</i>, <i>EP400</i>, <i>TUBA1C</i> and <i>AGAP2</i> were found. Of the 193 CpGs, 33 mapped to <i>ABCA2</i>, <i>ADORA2B</i>, <i>CTNNBIP1</i>, <i>KDM4B</i>, <i>NAA60</i>, <i>RSPH6A</i>, <i>SLC25A19</i> and <i>STIL</i> were significantly associated with DBP levels. Of the 33 CpGs, 12 within <i>ABCA2</i>, <i>SLC25A19</i>, <i>KDM4B</i>, <i>PTPRN2</i>, <i>DNASE1</i>, <i>TFCP2L1</i>, <i>LMNB2</i> and <i>C10orf71-AS1</i> negatively mediated the association between BMI and DBP, with a total mediation effect of -0.66 (95% CI [-1.07, -0.30]). Interestingly, BMI might also negatively mediate the association between the DNAm of most CpG mediators mentioned above and BP. The mediating effect of DNAm was also found when stratified by sex. In conclusion, DNAm variation may partially negatively mediate the association of BMI with BP. Our findings may provide new clues to further elucidate the pathogenesis of obesity to hypertension and identify new diagnostic biomarkers and therapeutic targets for hypertension.</p>","PeriodicalId":23446,"journal":{"name":"Twin Research and Human Genetics","volume":" ","pages":"18-29"},"PeriodicalIF":1.0000,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"DNA Methylation Mediated the Association of Body Mass Index With Blood Pressure in Chinese Monozygotic Twins.\",\"authors\":\"Jie Yao, Feng Ning, Weijing Wang, Dongfeng Zhang\",\"doi\":\"10.1017/thg.2024.3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Obesity is an established risk factor for hypertension, but the mechanisms are only partially understood. We examined whether body mass index (BMI)-related DNA methylation (DNAm) variation would mediate the association of BMI with blood pressure (BP). We first conducted a genomewide DNA methylation analysis in monozygotic twin pairs to detect BMI-related DNAm variation and then evaluated the mediating effect of DNAm on the relationship between BMI and BP levels using the causal inference test (CIT) method and mediation analysis. Ontology enrichment analysis was performed for CpGs using the GREAT tool. A total of 60 twin pairs for BMI and systolic blood pressure (SBP) and 58 twin pairs for BMI and diastolic blood pressure (DBP) were included. BMI was positively associated with SBP (β = 1.86, <i>p</i> = .0004). The association between BMI and DNAm of 85 CpGs reached <i>p</i> < 1×10<sup>-4</sup> level. Eleven BMI-related differentially methylated regions (DMRs) within <i>LNCPRESS1</i>, <i>OGDHL</i>, <i>RNU1-44P</i>, <i>NPHS1</i>, <i>ECEL1P2</i>, <i>LLGL2</i>, <i>RNY4P15</i>, <i>MOGAT3</i>, <i>PHACTR3</i>, and <i>BAI2</i> were found. Of the 85 CpGs, 9 mapped to <i>C10orf71-AS1</i>, <i>NDUFB5P1</i>, <i>KRT80</i>, <i>BAI2</i>, <i>ABCA2</i>, <i>PEX11G</i> and <i>FGF4</i> were significantly associated with SBP levels. Of the 9 CpGs, 2 within <i>ABCA2</i> negatively mediated the association between BMI and SBP, with a mediating effect of -0.24 (95% CI [-0.65, -0.01]). BMI was also positively associated with DBP (β = 0.60, <i>p</i> = .0495). The association between BMI and DNAm of 193 CpGs reached <i>p</i> < 1×10<sup>-4</sup> level. Twenty-five BMI-related DMRs within <i>OGDHL</i>, <i>POU4F2</i>, <i>ECEL1P2</i>, <i>TTC6</i>, <i>SMPD4</i>, <i>EP400</i>, <i>TUBA1C</i> and <i>AGAP2</i> were found. Of the 193 CpGs, 33 mapped to <i>ABCA2</i>, <i>ADORA2B</i>, <i>CTNNBIP1</i>, <i>KDM4B</i>, <i>NAA60</i>, <i>RSPH6A</i>, <i>SLC25A19</i> and <i>STIL</i> were significantly associated with DBP levels. Of the 33 CpGs, 12 within <i>ABCA2</i>, <i>SLC25A19</i>, <i>KDM4B</i>, <i>PTPRN2</i>, <i>DNASE1</i>, <i>TFCP2L1</i>, <i>LMNB2</i> and <i>C10orf71-AS1</i> negatively mediated the association between BMI and DBP, with a total mediation effect of -0.66 (95% CI [-1.07, -0.30]). Interestingly, BMI might also negatively mediate the association between the DNAm of most CpG mediators mentioned above and BP. The mediating effect of DNAm was also found when stratified by sex. In conclusion, DNAm variation may partially negatively mediate the association of BMI with BP. Our findings may provide new clues to further elucidate the pathogenesis of obesity to hypertension and identify new diagnostic biomarkers and therapeutic targets for hypertension.</p>\",\"PeriodicalId\":23446,\"journal\":{\"name\":\"Twin Research and Human Genetics\",\"volume\":\" \",\"pages\":\"18-29\"},\"PeriodicalIF\":1.0000,\"publicationDate\":\"2024-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Twin Research and Human Genetics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1017/thg.2024.3\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/31 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q4\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Twin Research and Human Genetics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1017/thg.2024.3","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/31 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
DNA Methylation Mediated the Association of Body Mass Index With Blood Pressure in Chinese Monozygotic Twins.
Obesity is an established risk factor for hypertension, but the mechanisms are only partially understood. We examined whether body mass index (BMI)-related DNA methylation (DNAm) variation would mediate the association of BMI with blood pressure (BP). We first conducted a genomewide DNA methylation analysis in monozygotic twin pairs to detect BMI-related DNAm variation and then evaluated the mediating effect of DNAm on the relationship between BMI and BP levels using the causal inference test (CIT) method and mediation analysis. Ontology enrichment analysis was performed for CpGs using the GREAT tool. A total of 60 twin pairs for BMI and systolic blood pressure (SBP) and 58 twin pairs for BMI and diastolic blood pressure (DBP) were included. BMI was positively associated with SBP (β = 1.86, p = .0004). The association between BMI and DNAm of 85 CpGs reached p < 1×10-4 level. Eleven BMI-related differentially methylated regions (DMRs) within LNCPRESS1, OGDHL, RNU1-44P, NPHS1, ECEL1P2, LLGL2, RNY4P15, MOGAT3, PHACTR3, and BAI2 were found. Of the 85 CpGs, 9 mapped to C10orf71-AS1, NDUFB5P1, KRT80, BAI2, ABCA2, PEX11G and FGF4 were significantly associated with SBP levels. Of the 9 CpGs, 2 within ABCA2 negatively mediated the association between BMI and SBP, with a mediating effect of -0.24 (95% CI [-0.65, -0.01]). BMI was also positively associated with DBP (β = 0.60, p = .0495). The association between BMI and DNAm of 193 CpGs reached p < 1×10-4 level. Twenty-five BMI-related DMRs within OGDHL, POU4F2, ECEL1P2, TTC6, SMPD4, EP400, TUBA1C and AGAP2 were found. Of the 193 CpGs, 33 mapped to ABCA2, ADORA2B, CTNNBIP1, KDM4B, NAA60, RSPH6A, SLC25A19 and STIL were significantly associated with DBP levels. Of the 33 CpGs, 12 within ABCA2, SLC25A19, KDM4B, PTPRN2, DNASE1, TFCP2L1, LMNB2 and C10orf71-AS1 negatively mediated the association between BMI and DBP, with a total mediation effect of -0.66 (95% CI [-1.07, -0.30]). Interestingly, BMI might also negatively mediate the association between the DNAm of most CpG mediators mentioned above and BP. The mediating effect of DNAm was also found when stratified by sex. In conclusion, DNAm variation may partially negatively mediate the association of BMI with BP. Our findings may provide new clues to further elucidate the pathogenesis of obesity to hypertension and identify new diagnostic biomarkers and therapeutic targets for hypertension.
期刊介绍:
Twin Research and Human Genetics is the official journal of the International Society for Twin Studies. Twin Research and Human Genetics covers all areas of human genetics with an emphasis on twin studies, genetic epidemiology, psychiatric and behavioral genetics, and research on multiple births in the fields of epidemiology, genetics, endocrinology, fetal pathology, obstetrics and pediatrics.
Through Twin Research and Human Genetics the society aims to publish the latest research developments in twin studies throughout the world.