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Objective To investigate the correlation between single nucleotide polymorphisms (SNPs) on the rs290481 site of TCF7L2 gene and type 2 diabetes mellitus complicated with coronary heart disease(CHD). Methods Peripheral blood DNA was extracted and TCF7L2 gene was amplified by polymerase chain reaction (PCR) and then sequenced in 120 patients with simple type 2 diabetes (T2DM), 120 patients with coronary heart disease (CHD), 120 patients with type 2 diabetes combined with coronary (T2DM+CHD) and 120 healthy controls. Chi-square test was used to analyze the difference of genotype frequency in four groups and binary logistic regression was used to analyze the risk factors of diabetes with coronary heart disease. Results The distribution frequency of AA, AG and GG on TCF7L2 and rs290481 SNP sites from T2DM group were significantly different with the controls, CHD group and T2DM plus CHD group respectively (P＜0.01). The serum level of HbAlc and GLU, was significantly different between AA and AG/GG genotypes (P＜0.05). Logistic regression data demonstrated that history of hypertension, HbAlc, GLU and the rs290481 AG/GG genotype of TCF7L2 were independent risk factors of diabetes mellitus complicated with CHD. Conclusions The polymorphism of TCF7L2 rs290481 gene is associated with the risk of type 2 diabetes complicated with CHD. AG/GG genotype confer a significantly increased risk of type 2 diabetes mellitus with CHD.

Objective: To investigate the gene mutation types and gene carrying rate of common thalassemia in patients with thalassemia in Quanzhou, and to analyze its molecular epidemiological characteristics in Quanzhou., Methods: 546 patients with thalassemia diagnosed at the first hospital of Quanzhou from January 2017 to October 2018 were collected and retrospectively analyzed for their types of mutations and carrier rates., Results: Among the 4226 samples submitted, 546 positive samples were detected, the total carrying rate of the thalassaemia genes was 12.92%; the carrier rate of α-thalassemia was 8.16%; the carrier rate of β-thalassemia was 4.76%; There were more α-thalassemia missing patients than non-deleted patients. The Southeast Asian deletion type (-- SEA /αα) was the most common one, with a composition ratio of 68.98%, which was followed by 22.61% (-α 3.7 /αα), 2.61% (α WS α/αα), and 2.32% (αα CS /αα), 2.32% (α QS α/αα), 1.16% (-α 4.2 /αα); 9 types of β-thalassemia gene mutations were detected. The most common three mutations were IVSII-654 (C→T, 42.29%), CD41-42 (-TTCT, 33.83%), CD17 (A→T, 12.94%). 2 cases of -- THAI /αα , 1 case of αα/ααα anti3.7 and 1 case of HKαα were detected., Conclusion: This study shows that the gene carrying rate of thalassemia in Quanzhou is high and has diversity, which can provide some reference for the prevention and control of thalassemia in Quanzhou.

Objective: To investigate the gene prevalence and spectrum of thalassemia in the women of childbearing age in quanzhou area., Methods: Venous blood of the women were collected for study, all subjects were registered in each county of quanzhou area by using cluster sampling. Both the mean corpuscular volume (MCV) and mean corpuscular hemoglobin (MCH) were used for screening thalassemia．Genotyping of the screened positive samples was performed by gap single polymerase chain reaction (gap-PCR) and reverse dot blot (RDB) hybridization．Unknown positive samples were analyzed with DNA sequencing., Results: Out of all 7 082 samples, Three hundred and eighty four were identified as thalassemia gene carriers with a carrying rate of 5.42 %. The α and β thalassemia were 3.21% and 2.15% respectively. -- SEA /αα was the most common genotype with 68.72 % in mutation types of α thalassemia, In addition gene, 2 cases of -- THAI /αα and 1 case of αα/ααα anti3.7 were also detected. IVS-Ⅱ-654/N and CD41-42/N were the most common gentypes with 75.00 % in mutation types of β thalassemia gene, 5 cases were found to be α β compogite thalassemia., Conclusion: The carrying rate of thalassemia gene in quanzhou area is higher, and with the most common gentypes including -- SEA /αα、IVSⅡ-654(C→T)/N and CD41-42(-TTCT)/N. The study results are beneficial for the screening of thalassemia in the genetic consultation and the prenatal gene diagnosis.