Yao, Sl., Wang, Q., Zhang, Zz. et al. Genome-wide association study on susceptibility genes associated with yang-deficiency constitution: A small sample case-control study., Chin. J. Integr. Med. 21, 601–609 (2015). https://doi.org/10.1007/s11655-014-1957-5
Shi-lin Yao, Qi Wang, Zu-zhi Zhang, et al. Genome-wide association study on susceptibility genes associated with yang-deficiency constitution: A small sample case-control study[J]. Chinese Journal of Integrative Medicine, 2015,21(8):601-609.
Yao, Sl., Wang, Q., Zhang, Zz. et al. Genome-wide association study on susceptibility genes associated with yang-deficiency constitution: A small sample case-control study., Chin. J. Integr. Med. 21, 601–609 (2015). https://doi.org/10.1007/s11655-014-1957-5DOI:
Shi-lin Yao, Qi Wang, Zu-zhi Zhang, et al. Genome-wide association study on susceptibility genes associated with yang-deficiency constitution: A small sample case-control study[J]. Chinese Journal of Integrative Medicine, 2015,21(8):601-609. DOI: 10.1007/s11655-014-1957-5.
Genome-wide association study on susceptibility genes associated with yang-deficiency constitution: A small sample case-control study
摘要
To explore susceptibility genes associated with yang-deficiency constitution using single nucleotide polymorphism (SNP) genotyping. Based on an epidemiological survey
30 volunteers with yang-deficiency constitution and 30 volunteers with a balanced constitution were included according to the Classification and Determination Standards of Constitutions in Traditional Chinese Medicine. Peripheral blood was collected and DNA was extracted from white blood cells. A genome-wide association study (GWAS) was conducted by SNP 6.0 genotyping at the Beijing CapitalBio Corporation Ltd. A minimum association P-value (Fisher’s exact value) of less than 10-4 in the allele
genotype
dominant
and recessive models served as the standard for significant association of SNP with yang-deficiency constitution. Among the four genetic models
a total of 42 SNPs were significantly associated with yang-deficiency constitution (Fisher’s exact P-values P<10-4). These SNPs were adjacent to more than 20 genes
including RGS6
mGluR5
GAPDHL19
and IKZF1. Yang-deficiency constitution exhibits the characteristics of polygenic inheritance. This pilot study suggests that the polymorphisms in RGS6
mGluR5
GAPDHL19
and IKZF1 are associated with changes in cyclic adenosine monophosphate and cyclic guanosine monophosphate levels
memory
metabolic energy status
and immune function
respectively in people with yang-deficiency constitution.
Abstract
To explore susceptibility genes associated with yang-deficiency constitution using single nucleotide polymorphism (SNP) genotyping. Based on an epidemiological survey
30 volunteers with yang-deficiency constitution and 30 volunteers with a balanced constitution were included according to the Classification and Determination Standards of Constitutions in Traditional Chinese Medicine. Peripheral blood was collected and DNA was extracted from white blood cells. A genome-wide association study (GWAS) was conducted by SNP 6.0 genotyping at the Beijing CapitalBio Corporation Ltd. A minimum association P-value (Fisher’s exact value) of less than 10-4 in the allele
genotype
dominant
and recessive models served as the standard for significant association of SNP with yang-deficiency constitution. Among the four genetic models
a total of 42 SNPs were significantly associated with yang-deficiency constitution (Fisher’s exact P-values P<10-4). These SNPs were adjacent to more than 20 genes
including RGS6
mGluR5
GAPDHL19
and IKZF1. Yang-deficiency constitution exhibits the characteristics of polygenic inheritance. This pilot study suggests that the polymorphisms in RGS6
mGluR5
GAPDHL19
and IKZF1 are associated with changes in cyclic adenosine monophosphate and cyclic guanosine monophosphate levels
memory
metabolic energy status
and immune function
respectively in people with yang-deficiency constitution.
关键词
yang-deficiency constitutiongenome-wide association analysissingle nucleotide polymorphismcase-control studyChinese Medicine
Keywords
yang-deficiency constitutiongenome-wide association analysissingle nucleotide polymorphismcase-control studyChinese Medicine
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相关机构
Georg-August-Universität Göttingen, Göttingen
The Key Laboratory of Geriatrics, Beijing Hospital and Beijing Institute of Geriatrics’ Ministry of Public Health
Medical Informatics Center, Peking University
Department of Hospital Management, Peking University Health Science Center, Peking University
Neurology Department of Peking University Third Hospital, Peking University