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1.
Biomedical and Environmental Sciences ; (12): 9-18, 2021.
Article in English | WPRIM | ID: wpr-878316

ABSTRACT

Objective@#The relationship between serum uric acid (SUA) levels and glycemic indices, including plasma glucose (FPG), 2-hour postload glucose (2h-PG), and glycated hemoglobin (HbA1c), remains inconclusive. We aimed to explore the associations between glycemic indices and SUA levels in the general Chinese population.@*Methods@#The current study was a cross-sectional analysis using the first follow-up survey data from The China Cardiometabolic Disease and Cancer Cohort Study. A total of 105,922 community-dwelling adults aged ≥ 40 years underwent the oral glucose tolerance test and uric acid assessment. The nonlinear relationships between glycemic indices and SUA levels were explored using generalized additive models.@*Results@#A total of 30,941 men and 62,361 women were eligible for the current analysis. Generalized additive models verified the inverted U-shaped association between glycemic indices and SUA levels, but with different inflection points in men and women. The thresholds for FPG, 2h-PG, and HbA1c for men and women were 6.5/8.0 mmol/L, 11.0/14.0 mmol/L, and 6.1/6.5, respectively (SUA levels increased with increasing glycemic indices before the inflection points and then eventually decreased with further increases in the glycemic indices).@*Conclusion@#An inverted U-shaped association was observed between major glycemic indices and uric acid levels in both sexes, while the inflection points were reached earlier in men than in women.


Subject(s)
Aged , Female , Humans , Male , Middle Aged , Asian People , Blood Glucose/analysis , China/epidemiology , Cohort Studies , Diabetes Mellitus/blood , Glucose Tolerance Test , Glycated Hemoglobin/analysis , Glycemic Index , Uric Acid/blood
2.
Chinese Medical Journal ; (24): 936-941, 2010.
Article in English | WPRIM | ID: wpr-242542

ABSTRACT

<p><b>BACKGROUND</b>Vaspin was recently identified as a novel adipokine that is predominantly secreted from adipose tissue and exerts insulin-sensitizing effects. This study was undertaken to elucidate the regulative effects of calorie control on the expression of vaspin and its potential mechanism.</p><p><b>METHODS</b>Diet-induced obese Sprague Dawley (SD) rats were adopted as experimental models and accepted interventions of various ingestions and pioglitazone. Various differentiated stages of cultured 3T3-L1 cells were dealt with pioglitazone or TNFalpha in vitro for 48 hours to further verify findings in animal experiments.</p><p><b>RESULTS</b>The rats were successfully induced into an obese experimental model with hyperinsulinemia, hyperlipidemia, and increased serum free fatty acid and TNFalpha by 12-week high-fat diet. It was found that depending on whether the rats were fed by a high-fat diet or a basal diet, there was extremely higher vaspin in the periepididymal fat pad than in subcutaneous adipose tissues by 16 weeks. Vaspin in sera and the periepididymal fat pad was much lower in rats with a high-fat diet than those with a basal diet (all P < 0.05), but vaspin in subcutaneous fat tissues was prone to increase in rats with a high-fat diet. A 4-week calorie restriction or pioglitazone on the obese rats resulted in a partial recovery of vaspin levels in sera and periepididymal adipose tissues, especially the latter revealed a more obvious superiority and increased vaspin levels of subcutaneous adipose. Surprisingly, the treatment of 4-week high-fat diet on non-obese rats did not significantly depress vaspin of sera and periepididymal adipose tissues. However, it is unknown if re-feeding generated the effect on vaspin levels of obese and non-obese rats on sera or adipose tissues. The correlation analysis showed that vaspin levels of serum and periepididymal fat tissues were negatively correlated with serum FFA, TNFalpha and insulin; meanwhile, there was a positive correlation between serum vaspin and vaspin of periepididymal fat tissues. Pioglitazone enhanced vaspin levels in cultured 3T3-L1 cells and supernatant in various differentiated stages, and this effect became more and more obvious along with the change of preadipocytes into mature fat cells. Administration of TNFalpha caused suppression on vaspin expression in differentiated stages of 3T3-L1 cells.</p><p><b>CONCLUSIONS</b>The present data indicated that a long-term high-fat diet could induce obesity metabolic syndrome in SD rats and finally lead to lower vaspin of sera and periepididymal fat, while pioglitazone and chronic calorie-control ingestion could enhance the production of vaspin. It was undoubtedly demonstrated that vaspin expression was strongly associated with insulin sensitivity, serum FFA, and TNFalpha.</p>


Subject(s)
Animals , Male , Mice , Rats , 3T3-L1 Cells , Adipose Tissue , Metabolism , Blotting, Western , Body Weight , Cell Differentiation , Dietary Fats , Fatty Acids, Nonesterified , Insulin , Blood , Obesity , Blood , Metabolism , Rats, Sprague-Dawley , Serpins , Blood , Metabolism , Thiazolidinediones , Pharmacology , Tumor Necrosis Factor-alpha , Blood
3.
Chinese Journal of Medical Genetics ; (6): 11-15, 2009.
Article in Chinese | WPRIM | ID: wpr-307979

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the clinical features and to identify the DAX-1 gene mutation in a Chinese kindred with X-linked adrenal hypoplasia congenital(AHC).</p><p><b>METHODS</b>Clinical data and peripheral blood samples were obtained from the affected individuals and their relatives. The genomic DNA was isolated from whole blood. Four pairs of primers were used to amplify the two exons of the DAX-1 gene, and PCR products were purified and sequenced directly. Sequencing results were compared to the human DAX-1 sequence in the public database.</p><p><b>RESULTS</b>A novel hemizygous frameshift mutation (428delG) in exon 1 of the DAX-1 gene was found in both patients (the index case and his cousin). Some clinical features such as the age of onset were different although these 2 patients carried the same mutation. Three females in the family, including the mothers of the 2 patients and their grandmother were carriers of this mutation. No such mutation was detected in other healthy persons in the family.</p><p><b>CONCLUSION</b>The result suggested that X-linked AHC in the kindred was caused by a novel mutation of 428delG in the DAX-1 gene, and the same mutation can give rise to variable phenotypes.</p>


Subject(s)
Adolescent , Child , Female , Humans , Male , Adrenal Hyperplasia, Congenital , Genetics , Pathology , Asian People , Genetics , Base Sequence , DAX-1 Orphan Nuclear Receptor , DNA-Binding Proteins , Genetics , Genetic Diseases, X-Linked , Genetics , Pathology , Mutation , Pedigree , Phenotype , Receptors, Retinoic Acid , Genetics , Repressor Proteins , Genetics , Sequence Analysis, DNA
4.
Journal of Forensic Medicine ; (6): 141-143, 2006.
Article in Chinese | WPRIM | ID: wpr-983163

ABSTRACT

OBJECTIVE@#To found the quantifiable index of "The severe degree of negligence" in describing the general severity degree of medical malpractice or medical dispute.@*METHODS@#"The severe degree of negligence" can be calculated by the way of multiplying the coefficient of medical malpractice's grade by the coefficient of responsibility degree.@*RESULTS@#There are 15 grades of "The severe degree of negligence" through calculation, from the severest degree of 1 to the lightest degree of 20.@*CONCLUSION@#"The severe degree of negligence" can give an order of severe degree to different grade and different responsibility of medical malpractice. According to this order, the operation of medical malpractice and medical dispute settle will be easier and more rationality.


Subject(s)
Humans , Expert Testimony/legislation & jurisprudence , Forensic Medicine , Liability, Legal , Malpractice/legislation & jurisprudence , Medical Errors/legislation & jurisprudence
5.
Chinese Journal of Medical Genetics ; (6): 698-701, 2005.
Article in Chinese | WPRIM | ID: wpr-279964

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the distribution of SNP276 in adiponectin gene in Chinese Hans and its impact on type 2 diabetes mellitus and insulin sensitivity.</p><p><b>METHODS</b>The study population consisted of 417 Chinese Hans residents in Anhui province, including 141 subjects with normal glucose tolerance (NGT) and 276 with type 2 diabetes (T2DM). The islet beta-cell insulin secretion and tissue insulin sensitivity were assessed by formulae of homeostasis model assessment (HOMA-IR & HOMA beta). Firstly, polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) was used to determine whether variation exists in APM1. Then, exact variation was detected by automated DNA direct sequencing.</p><p><b>RESULTS</b>The genotypes of APM1 SNP276 were 0.489 GG, 0.418 GT and 0.092 TT and the major allele was G (frequency=0.699) in subjects with NGT. The distributions of genotypes and alleles of SNP276 both displayed significant difference between NGT and T2DM groups (P=0.031 and 0.013). The SNP276 non-TT (TG+GG) genotype was associated with increased risk of T2DM (OR=2.447, 95%CI: 1.067-5.612, P=0.035). In T2DM group, the subjects with SNP276 GG or GT genotype had higher body mass index, body fat content, fasting plasma glucose and HOMA-IR than did those with TT genotype (P < 0.05 or P < 0.01). Besides, GG genotype had higher systolic blood pressure (P=0.021). In NGT group, SNP276 non-TT carrier had increased body mass index, body fat content, waist hip ratio, fasting plasma insulin, oral glucose tolerance test 2 h plasma insulin and HOMA-IR when compared with TT genotype (P < 0.05 or 0.01).</p><p><b>CONCLUSION</b>SNP276 in APM1 was associated with T2DM and insulin sensitivity.</p>


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Adiponectin , Genetics , Base Sequence , Blood Glucose , Metabolism , Diabetes Mellitus, Type 2 , Blood , Genetics , Gene Frequency , Genetic Predisposition to Disease , Genetics , Genotype , Insulin , Blood , Insulin Resistance , Polymerase Chain Reaction , Polymorphism, Single Nucleotide , Polymorphism, Single-Stranded Conformational , Sequence Analysis, DNA
6.
Chinese Journal of Medical Genetics ; (6): 29-31, 2004.
Article in Chinese | WPRIM | ID: wpr-329406

ABSTRACT

<p><b>OBJECTIVE</b>To determine whether the muscle-specific glycogen-targeting regulatory subunit of the glucogen bound protein phosphatase 1 (PPP1R3) gene 5 bp deletion/insertion(D/I) within 3'-untranslated region ( 3'-UTR) polymorphism is associated with type 2 diabetes in Chinese Han population in Hefei region of Anhui province.</p><p><b>METHODS</b>The PPP1R3 gene 3'-UTR 5 bp D/I polymorphism was detected by polymerase chain reaction in 268 patients with type 2 diabetes and 106 normal controls.</p><p><b>RESULTS</b>(1) The distributions of the frequency of three genotypes and two alleles of the PPP1R3 gene 5 bp D/I polymorphism showed no significant difference between the type 2 diabetic cases and the normal controls. (2) In both the cases and controls, there was no significant difference in age at onset, duration of disease, blood glucose, blood lipid profile, blood pressure, insulin sensitive index, body mass index, and waist hip ratio between the three genotypic groups(P 0.05). (3) The PPP1R3 gene 3'-UTR polymorphism in Chinese Han population in Hefei region of Anhui province was found to be similar to that in both Japanese population and Canadian population, and to be different from that in Piman Indians and the Caucasians in Sweden.</p><p><b>CONCLUSION</b>The PPP1R3 gene 5 bp D/I within 3'-UTR polymorphism taking on genetic variation among the different races of mankind may not play a critical role in the development of type 2 diabetes mellitus in Chinese Hans of Hefei region in Anhui province.</p>


Subject(s)
Aged , Female , Humans , Male , Middle Aged , 3' Flanking Region , Genetics , Alleles , Diabetes Mellitus, Type 2 , Genetics , Pathology , Gene Frequency , Genotype , Mutagenesis, Insertional , Phosphoprotein Phosphatases , Genetics , Polymorphism, Genetic , Protein Phosphatase 1 , Sequence Deletion
7.
Chinese Journal of Epidemiology ; (12): 534-536, 2004.
Article in Chinese | WPRIM | ID: wpr-342317

ABSTRACT

<p><b>OBJECTIVE</b>To study the association of muscle-specific glycogen-targeting regulatory subunit of the glucogen-bound protein phosphatase 1 (PPP1R3) gene codon 905 Asp/Tyr polymorphism with type 2 diabetes in Chinese Han population in Hefei region of Anhui province.</p><p><b>METHODS</b>PPP1R3 gene Asp905Tyr polymorphism was detected by polymerase chain reaction and appropriate restriction enzyme (PCR-RFLP) in 262 type 2 diabetic cases and 104 normal controls. Case and control groups were divided into subgroups by body mass index (BMI) 25 kg/m2.</p><p><b>RESULTS</b>When PPP1R3 gene Asp905Tyr polymorphism was not associated with type 2 diabetes mellitus. When subjects with BMI < 25 kg/m2 and Tyr/Tyr genotypes were used as reference. Subjects with Asp905 and BMI > or = 25 kg/m2 had a 3.69-fold increase of risk suffering from type 2 diabetes (OR = 3.69, 95% CI: 1.38-8.89, P=0.006).</p><p><b>CONCLUSIONS</b>PPP1R3 gene Asp905Tyr polymorphism did not seem to play a critical role in the development of type 2 diabetes mellitus in Han population of Chinese in Anhui province but interaction between the Asp905 and BMI cause the increase of risk of type 2 diabetes.</p>


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Alleles , Aspartic Acid , Genetics , China , Epidemiology , Ethnology , Diabetes Mellitus, Type 2 , Epidemiology , Genetics , Gene Frequency , Genotype , Obesity , Phosphoprotein Phosphatases , Genetics , Polymerase Chain Reaction , Polymorphism, Genetic , Polymorphism, Restriction Fragment Length , Protein Phosphatase 1 , Risk Factors , Tyrosine , Genetics
8.
Chinese Journal of Endocrinology and Metabolism ; (12)2001.
Article in Chinese | WPRIM | ID: wpr-676134

ABSTRACT

The effects of pioglitazone (PIO) and tumor necrosis faetor-?(TNF-?) on two kinds of adiponectin receptor (AdipoR) mRNA expression were observed in 3T3-L1 adipocytes by RT-PCR.AdipoR mRNA expression was up-regulated during 3T3-L1 preadipocyte differentiation;PIO could increase the AdipoR mRNA level expressed in undifferentiated and differentiated 3T3-L1 adipocytes in a time-and dose-dependent manner,and TNF-?had no influence on the expression of AdipoR mRNA.

9.
Chinese Journal of Endocrinology and Metabolism ; (12)2000.
Article in Chinese | WPRIM | ID: wpr-676241

ABSTRACT

The expression of adiponectin mRNA in greater omentum fat tissue was measured in 43 subjects using RT-PCR.The results showed that the expression of adiponectin mRNA in greater omentum fat tissue was significantly lower in obese subjects than that in normal persons,and abdominal obesity,HOMA-IR and tumor necrosis factor-?were the main independent factors influencing the expression of adiponectin mRNA in greater omentum.

10.
Chinese Journal of Endocrinology and Metabolism ; (12)1985.
Article in Chinese | WPRIM | ID: wpr-676338

ABSTRACT

Undifferentiated and differentiated 3T3-L1 adipocytes were treated with 100 ng/ml tumor necrosis factor-?(TNF-?),and peroxisome proliferator-activated receptor-?2 (PPAR-?2) mRNA expression and adiponectin secretion in cultured cells were measured.The results showed that TNF-?suppressed PPAR-?2 mRNA expression and adiponeetin secretion in 3T3-L1 adipocytes (P

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