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- Publisher Website: 10.1136/jech-2013-203451
- Scopus: eid_2-s2.0-84904185092
- PMID: 24737458
- WOS: WOS:000339723200015
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Article: Genetically predicted 17β-estradiol and systemic inflammation in women: A separate-sample Mendelian randomisation analysis in the Guangzhou Biobank cohort study
Title | Genetically predicted 17β-estradiol and systemic inflammation in women: A separate-sample Mendelian randomisation analysis in the Guangzhou Biobank cohort study |
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Authors | |
Issue Date | 2014 |
Citation | Journal of Epidemiology and Community Health, 2014, v. 68, n. 8, p. 780-785 How to Cite? |
Abstract | Background: Many chronic diseases are characterised by low-grade systemic inflammation. Oestrogens may promote immune response consistent with sex-specific patterns of diseases. In vitro culture and animal experiments suggest oestrogens are anti-inf lammatory and might thereby protect against low-grade systemic inflammation. Evidence from epidemiological studies is limited. Using a Mendelian randomisation analysis with a separate-sample instrumental variable (SSIV) estimator, we examined the association of genetically predicted 17β-estradiol with well-established systemic inflammatory markers (total white cell count, granulocyte and lymphocyte count). Methods: A genetic score predicting 17β-estradiol was developed in 237 young Chinese women (university students) from Hong Kong based on a parsimonious set of genetic polymorphisms (ESR1 (rs2175898) and CYP19A1 (rs1008805)). Multivariable linear regression was used to examine the association of genetically predicted 17β-estradiol with systemic inflammatory markers among 3096 older (50+ years) Chinese women from the Guangzhou Biobank Cohort Study. Results: Predicted 17β-estradiol was negatively associated with white blood cell count (-6.3 103/mL, 95% CI -11.4 to -1.3) and granulocyte count (-4.5 10 3 /mL, 95% CI -8.5 to -0.4) but not lymphocyte count (-1.5 10 3 /mL, 95% CI -3.4 to 0.4) adjusted for age only. Results were similar further adjusted for education, smoking, use of alcohol, physical activity, Body Mass Index, waist-hip ratio, age of menarche, age at menopause, use of hormonal contraceptives and hormone replacement therapy. Conclusions: Endogenous genetically predicted 17β-estradiol reduced low-grade systemic inflammatory markers (white blood cell count and granulocyte count), consistent with experimental and ecological evidence of 17β-estradiol promoting immune response. Replication in a larger sample is required. |
Persistent Identifier | http://hdl.handle.net/10722/249723 |
ISSN | 2023 Impact Factor: 4.9 2023 SCImago Journal Rankings: 2.091 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Zhao, J. | - |
dc.contributor.author | Jiang, C. Q. | - |
dc.contributor.author | Lam, T. H. | - |
dc.contributor.author | Liu, B. | - |
dc.contributor.author | Cheng, K. K. | - |
dc.contributor.author | Kavikondala, S. | - |
dc.contributor.author | Zhang, W. S. | - |
dc.contributor.author | Leung, G. M. | - |
dc.contributor.author | Schooling, C. M. | - |
dc.date.accessioned | 2017-11-28T02:13:06Z | - |
dc.date.available | 2017-11-28T02:13:06Z | - |
dc.date.issued | 2014 | - |
dc.identifier.citation | Journal of Epidemiology and Community Health, 2014, v. 68, n. 8, p. 780-785 | - |
dc.identifier.issn | 0143-005X | - |
dc.identifier.uri | http://hdl.handle.net/10722/249723 | - |
dc.description.abstract | Background: Many chronic diseases are characterised by low-grade systemic inflammation. Oestrogens may promote immune response consistent with sex-specific patterns of diseases. In vitro culture and animal experiments suggest oestrogens are anti-inf lammatory and might thereby protect against low-grade systemic inflammation. Evidence from epidemiological studies is limited. Using a Mendelian randomisation analysis with a separate-sample instrumental variable (SSIV) estimator, we examined the association of genetically predicted 17β-estradiol with well-established systemic inflammatory markers (total white cell count, granulocyte and lymphocyte count). Methods: A genetic score predicting 17β-estradiol was developed in 237 young Chinese women (university students) from Hong Kong based on a parsimonious set of genetic polymorphisms (ESR1 (rs2175898) and CYP19A1 (rs1008805)). Multivariable linear regression was used to examine the association of genetically predicted 17β-estradiol with systemic inflammatory markers among 3096 older (50+ years) Chinese women from the Guangzhou Biobank Cohort Study. Results: Predicted 17β-estradiol was negatively associated with white blood cell count (-6.3 103/mL, 95% CI -11.4 to -1.3) and granulocyte count (-4.5 10 3 /mL, 95% CI -8.5 to -0.4) but not lymphocyte count (-1.5 10 3 /mL, 95% CI -3.4 to 0.4) adjusted for age only. Results were similar further adjusted for education, smoking, use of alcohol, physical activity, Body Mass Index, waist-hip ratio, age of menarche, age at menopause, use of hormonal contraceptives and hormone replacement therapy. Conclusions: Endogenous genetically predicted 17β-estradiol reduced low-grade systemic inflammatory markers (white blood cell count and granulocyte count), consistent with experimental and ecological evidence of 17β-estradiol promoting immune response. Replication in a larger sample is required. | - |
dc.language | eng | - |
dc.relation.ispartof | Journal of Epidemiology and Community Health | - |
dc.title | Genetically predicted 17β-estradiol and systemic inflammation in women: A separate-sample Mendelian randomisation analysis in the Guangzhou Biobank cohort study | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1136/jech-2013-203451 | - |
dc.identifier.pmid | 24737458 | - |
dc.identifier.scopus | eid_2-s2.0-84904185092 | - |
dc.identifier.hkuros | 230833 | - |
dc.identifier.volume | 68 | - |
dc.identifier.issue | 8 | - |
dc.identifier.spage | 780 | - |
dc.identifier.epage | 785 | - |
dc.identifier.eissn | 1470-2738 | - |
dc.identifier.isi | WOS:000339723200015 | - |
dc.identifier.issnl | 0143-005X | - |