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DOI 10.18632/oncotarget.9193

Медицинская библиотека · Oncotarget · 2016

VPO1 mediates oxidation of LDL and formation of foam cells.

Cai Liangchun, Wen Junping, Yao Jin, Li Liantao, Lin Wei, Liang Jixing, Lin Lixiang, Huang Huibin, Zheng Yanhui, Chen Gang

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Аннотация

OBJECTIVE

To examine receptors for advanced glycation end-products Gly82Ser polymorphism in patients of type 2 diabetes with comorbid depression.

METHODS

The case-control study was conducted at Fujian Provincial Hospital, Fuzhou, China, between December 2011 and December 2012, and comprised unrelated Chinese Han patients of type 2 diabetes, and diabetics with diagnosed clinical depression. Gly82Ser polymorphism polymorphism was determined using polymerase chain reaction amplification-high resolution melting curve protocol. Serum levels of endogenous secretory receptor for advanced glycation end products were measured using enzyme-linked immunosorbent assay. SPSS 16 was used for data analysis.

RESULTS

Of the 114 subjects, 72(63.15%) were clinically depressed. Lower levels of endogenous secretory receptor were found in the depression group compared with the other group (p=0.049). No difference in genotypes or allele frequencies existed between the two groups (p>0.05). Gly82Ser carriers had significantly higher Hamilton Rating Scale scores (p<0.001) and lower serum endogenous secretory receptor (p=0.012) among the depressed diabetics. There were also significant differences in body mass index (p=0.005), abdominal circumference (p=0.038), carotid intima-media thickness (p=0.037) and high-sensitivity C-reactive protein (p=0.005) concentration between the different genotypes..

CONCLUSIONS

Receptors for advanced glycation end-products-ligands system may be involved in type 2 diabetes with comorbid depression at the genetic level.

Для цитирования: Cai Liangchun, Wen Junping, Yao Jin, Li Liantao, Lin Wei, Liang Jixing, Lin Lixiang, Huang Huibin, Zheng Yanhui, Chen Gang. VPO1 mediates oxidation of LDL and formation of foam cells.. Oncotarget. 2016. DOI: 10.18632/oncotarget.9193.

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