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Association study of gene polymorphisms and depression with abnormal humor in traditional Uighur medicine
BACKGROUND: According to the humor theory of Traditional Uighur Medicine (TUM), a same disease is classified into different abnormal humor types and corresponding methods are applied to treat the diseases according to the type of abnormal humor characteristics. To date the biological foundation of c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222500/ https://www.ncbi.nlm.nih.gov/pubmed/24274373 http://dx.doi.org/10.1186/1472-6882-13-332 |
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author | Yusup, Abdiryim Upur, Hanzohra Abla, Ayimgul Upur, Halmurat |
author_facet | Yusup, Abdiryim Upur, Hanzohra Abla, Ayimgul Upur, Halmurat |
author_sort | Yusup, Abdiryim |
collection | PubMed |
description | BACKGROUND: According to the humor theory of Traditional Uighur Medicine (TUM), a same disease is classified into different abnormal humor types and corresponding methods are applied to treat the diseases according to the type of abnormal humor characteristics. To date the biological foundation of classification of diseases by humor theory has been little studied and the mechanism of action is still unclear. In the present study, we aimed to investigate the association between some related gene polymorphisms and depression with abnormal humor in TUM. METHODS: 201 cases of depression patients in a Uighur population were divided into two groups as: 107 cases of depression patients with abnormal black bile (ABB), 94 cases of depression patients with none abnormal black bile (nABB), and 50 healthy people were served as control group. Venous blood was used to isolate DNA samples, and the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique was used for genotyping of single nucleotide polymorphisms (SNPs). Polymorphisms in the serotonin 2A (5-HT(2A)) receptor gene, brain derived neurotrophic factor (BDNF), serotonin 1A (5-HT(1A)) receptor gene were investigated in each groups, respectively. RESULTS: The 5-HT(2A) A-1438G, 5-HT(2A) T102C, BDNF Val66Met, and 5-HT(1A) C-1019G gene polymorphisms showed significant association with ABB. However, no difference between nABB and controls was found for those genotype distribution and allele frequency. Moreover, the T102C and A1438G SNPs in the 5-HT(2A) receptor gene polymorphisms were in linkage disequilibrium. In addition, the OR associated with the combination of Val66Met-Val/Val genotype plus the presence of -1019C allele was 8.393 for ABB compared with controls (OR 8.393; 95% CI 1.807 ~ 38.991; P= 0.003). Moreover, the OR associated with the presence of -Met plus -1019C alleles was 12.194 for ABB compared with controls (OR 12.194; 95% CI 1.433 ~ 103.776; P= 0.005). The OR associated with the presence of -1438C/C plus Val/Val genotypes was 7.738 for ABB compared with controls (OR 7.738; 95% CI 1.566 ~ 38.241; P= 0.005). CONCLUSION: It was concluded that there were significant relationship between the gene polymorphisms and classification of depression with abnormal humor in TUM. The 5-HT(2A) A-1438G, 5-HT(2A) T102C, BDNF Val66Met, and 5-HT(1A) C-1019G gene polymorphisms might predict the incidence of depression with ABB. |
format | Online Article Text |
id | pubmed-4222500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42225002014-11-07 Association study of gene polymorphisms and depression with abnormal humor in traditional Uighur medicine Yusup, Abdiryim Upur, Hanzohra Abla, Ayimgul Upur, Halmurat BMC Complement Altern Med Research Article BACKGROUND: According to the humor theory of Traditional Uighur Medicine (TUM), a same disease is classified into different abnormal humor types and corresponding methods are applied to treat the diseases according to the type of abnormal humor characteristics. To date the biological foundation of classification of diseases by humor theory has been little studied and the mechanism of action is still unclear. In the present study, we aimed to investigate the association between some related gene polymorphisms and depression with abnormal humor in TUM. METHODS: 201 cases of depression patients in a Uighur population were divided into two groups as: 107 cases of depression patients with abnormal black bile (ABB), 94 cases of depression patients with none abnormal black bile (nABB), and 50 healthy people were served as control group. Venous blood was used to isolate DNA samples, and the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique was used for genotyping of single nucleotide polymorphisms (SNPs). Polymorphisms in the serotonin 2A (5-HT(2A)) receptor gene, brain derived neurotrophic factor (BDNF), serotonin 1A (5-HT(1A)) receptor gene were investigated in each groups, respectively. RESULTS: The 5-HT(2A) A-1438G, 5-HT(2A) T102C, BDNF Val66Met, and 5-HT(1A) C-1019G gene polymorphisms showed significant association with ABB. However, no difference between nABB and controls was found for those genotype distribution and allele frequency. Moreover, the T102C and A1438G SNPs in the 5-HT(2A) receptor gene polymorphisms were in linkage disequilibrium. In addition, the OR associated with the combination of Val66Met-Val/Val genotype plus the presence of -1019C allele was 8.393 for ABB compared with controls (OR 8.393; 95% CI 1.807 ~ 38.991; P= 0.003). Moreover, the OR associated with the presence of -Met plus -1019C alleles was 12.194 for ABB compared with controls (OR 12.194; 95% CI 1.433 ~ 103.776; P= 0.005). The OR associated with the presence of -1438C/C plus Val/Val genotypes was 7.738 for ABB compared with controls (OR 7.738; 95% CI 1.566 ~ 38.241; P= 0.005). CONCLUSION: It was concluded that there were significant relationship between the gene polymorphisms and classification of depression with abnormal humor in TUM. The 5-HT(2A) A-1438G, 5-HT(2A) T102C, BDNF Val66Met, and 5-HT(1A) C-1019G gene polymorphisms might predict the incidence of depression with ABB. BioMed Central 2013-11-25 /pmc/articles/PMC4222500/ /pubmed/24274373 http://dx.doi.org/10.1186/1472-6882-13-332 Text en Copyright © 2013 Yusup et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Yusup, Abdiryim Upur, Hanzohra Abla, Ayimgul Upur, Halmurat Association study of gene polymorphisms and depression with abnormal humor in traditional Uighur medicine |
title | Association study of gene polymorphisms and depression with abnormal humor in traditional Uighur medicine |
title_full | Association study of gene polymorphisms and depression with abnormal humor in traditional Uighur medicine |
title_fullStr | Association study of gene polymorphisms and depression with abnormal humor in traditional Uighur medicine |
title_full_unstemmed | Association study of gene polymorphisms and depression with abnormal humor in traditional Uighur medicine |
title_short | Association study of gene polymorphisms and depression with abnormal humor in traditional Uighur medicine |
title_sort | association study of gene polymorphisms and depression with abnormal humor in traditional uighur medicine |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222500/ https://www.ncbi.nlm.nih.gov/pubmed/24274373 http://dx.doi.org/10.1186/1472-6882-13-332 |
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