|Year : 2015 | Volume
| Issue : 1 | Page : 31
Association of adiponectin gene polymorphism with adiponectin levels and risk for insulin resistance syndrome
Jai Prakash1, Balraj Mittal2, Shally Awasthi3, Neena Srivastava4
1 Department of Physiology, King George's Medical University, Lucknow, Uttar Pradesh; Department of Pediatrics, King George's Medical University, Lucknow, Uttar Pradesh, India
2 Department of Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India
3 Department of Pediatrics, King George's Medical University, Lucknow, Uttar Pradesh, India
4 Department of Physiology, King George's Medical University, Lucknow, Uttar Pradesh, India
|Date of Submission||16-Jul-2014|
|Date of Acceptance||10-Mar-2015|
|Date of Web Publication||08-Apr-2015|
Department of Physiology, King George's Medical University, Lucknow, Uttar Pradesh
Source of Support: None, Conflict of Interest: None
Background: Adiponectin is an abundant adipose tissue-derived protein with anti-atherogenic, anti-inflammatory and antidiabetic properties. Plasma adiponectin levels are decreased in obesity, type 2 diabetes, and coronary artery disease and low adiponectin levels also predict insulin resistance (IR).
Methods: Case-control study in which 642 male and female subjects were participated from the North Indian population. Lipid, insulin, leptin and adiponectin level were estimated using standard protocols by commercially available test kits. Single nucleotide polymorphisms +45T>G and +276G>T of the AMP1 (adiponectin) gene was genotyped by polymerase chain reaction restriction fragment length polymorphism method.
Results: Levels of adiponectin, insulin, homeostasis model assessment-IR index (HOMA-IR index), systolic blood pressure and fat mass showed significant differences between male and female subjects. Serum adiponectin level showed highly significant association with both the +45 and the +276 genotypes. The common haplotype triglyceride (TG) showed a significantly lower adiponectin value than other haplotypes (P = 0.0001). A clear trend of decreasing adiponectin levels per copy of the common haplotype was observed. Nonobese insulin sensitive subjects showed a higher adiponectin value (P = 0.0006) than nonobese insulin resistant subjects. The values of blood pressure, adiponectin, insulin, HOMA-IR, total-cholesterol, and low-density lipoprotein-cholesterol significantly associated with TG haplotype.
Conclusions: We observed the very strong association of the adiponectin 45-276 genotypes and haplotypes with adiponectin levels in healthy north Indian population and TG haplotypes also associated with metabolic parameters of the IR syndrome.
Keywords: Adiponectin, AMP1, haplotype, insulin resistance, polymorphism
|How to cite this article:|
Prakash J, Mittal B, Awasthi S, Srivastava N. Association of adiponectin gene polymorphism with adiponectin levels and risk for insulin resistance syndrome. Int J Prev Med 2015;6:31
|How to cite this URL:|
Prakash J, Mittal B, Awasthi S, Srivastava N. Association of adiponectin gene polymorphism with adiponectin levels and risk for insulin resistance syndrome. Int J Prev Med [serial online] 2015 [cited 2020 Aug 6];6:31. Available from: http://www.ijpvmjournal.net/text.asp?2015/6/1/31/154773
| Introduction|| |
Adipose tissue is an active endocrine organ that secretes adiponectin,  which is a potent insulin sensitizer in muscle and liver, regulating energy homeostasis and glucose tolerance.  There is large evidence that the adipose tissue is an active endocrine organ, not only the major tissue for energy storage and secreting a different type of proteins that influence the metabolism of the body and affect energy and glucose homeostasis.  Adiponectin is the product of the AMP1 (Adiponectin) gene, which spans approximately 15.8 kb and three exons. It is sited on chromosome 3q27, which has been linked to a susceptibility locus for metabolic syndrome, type 2 diabetes and cardiovascular disease. 
In a previous study, adiponectin concentrations were positively correlated with insulin sensitivity and decreased significantly with deteriorating glucose tolerance in Pima Indians and Caucasians,  while adiponectin concentrations increased after weight reduction.  In addition, administration of intravenous recombinant adiponectin to rodent models of insulin resistance (IR) restored normal insulin sensitivity. 
In animal model of obesity and diabetes, administration of adiponectin or its globular domain produces weight loss and improves insulin sensitivity and glucose tolerance. The adiponectin acts on skeletal muscle to increase fatty acid oxidation and on liver to increase sensitivity to the anti-gluconeogenesis effects of insulin. , With such profound effects on metabolism, genetic variability in adiponectin may be a determinant of IR. Results of two linkage studies are consistent with this hypothesis: A genome scan for IR loci in U.S. Caucasian families detected a signal at 3q27 the locus of the AMP1 gene.  The early-onset type 2 diabetes has been linked to the same position in French families.  In addition, association study from Japan points out these linkage results directly to the AMP1 gene. The gene is very polymorphic; associations with adiponectin level and/or the metabolic syndrome have been reported for genetic variants in many populations.
Two single nucleotide polymorphisms in the AMP1 gene, a silent T to G substitution in exon 2, 45T > G (rs2241766) and another G to T substitution in intron 2, 276 G > T (rs266729) have been associated with adiponectin levels, obesity, type 2 diabetes and coronary artery disease patients, although there are inconsistencies among these results. ,,,,,,,,
Therefore, in the present study, we investigated the association of AMP1 45-276 genotypes and haplotypes with serum adiponectin levels and their association with IR syndrome, in large ethnically homogeneous and healthy northern Indian population.
| Methods|| |
All individuals were of north Indian origin, and the population was homogeneous with regard to ethnic background. A total of 642 subjects were enrolled from the out patients department of King George's Medical University, Lucknow and volunteers from the general population of Lucknow (Uttar Pradesh, India). Of these, 88.20% were Hindu north Indian (Hindi spoken residing in Lucknow) while 21.8% represented other religions or languages. The possibility of population admixture was slight, because, in this part of the country, inter-religion marriage is very rare because of the traditional socioeconomic differences among different religions (for details).  309 obese (body mass index [BMI] >30 kg/m 2 ) and 333 nonobese (BMI ≤ 30 kg/m 2 ) individual were selected on the basis of the BMI. In all subjects, body height, body weight, waist circumferences and hip circumferences were measured for the calculation of BMI and waist to hip ratio. Subjects with established diabetes mellitus, coronary artery disease, congestive heart failure, and pregnant women were excluded. Subjects were classified as type 2 diabetics if they were on hypoglycemic medications or when their fasting glucose concentrations exceeded 126 mg/dL. Tobacco smokers (12.6%) included subjects with present or past smoking or any other tobacco use. About alcohol usage, 88.6% were nonalcoholic. In our study participants, 56.1% of participants were pure vegetarians (no consumption of meat, egg or fish). Informed consent was obtained from each participant, and the study was carried out in accordance with the local ethics committee. At baseline, all study participants were subjected to a thorough screening program that included assessment of a detailed personal and family history, physical examination, determination of anthropometric indices and measurement of various biochemical parameters.
Estimation of body fat composition
The body composition was measured by bioelectrical impedance analyzer (Tanita-TBF-310, Tokyo, Japan). The impedance measurements were obtained on the morning of the examination after the individuals had voided while fasting. The results obtained were BMI, the body fat mass, fat-FM, and percent of body fat (fat %).
Venous blood was collected after an overnight fast, and plasma, and serum samples were either used immediately for analysis or were stored frozen at −80°C. Commercial enzymatic test kits were used for determining high-density lipoprotein-cholesterol (HDL-C), triglyceride (TG) concentrations and total-cholesterol (T-cholesterol), low-density lipoprotein-cholesterol (LDL-C) was calculated by the formula of Friedewald (LDL-C = T-cholesterol − HDL-C − TG/5 mg/dL). Insulin level was determined by enzyme-linked radio immunosorbent assay (Linco Research, St Charles, USA). The degree of insulin sensitivity/resistance was calculated according to the homeostasis model assessment (HOMA) which is a good index for assessing insulin sensitivity/resistance. IR was calculated as follows: IR = FI × g/22.5; where FI = fasting insulin (μu/mL) and g = fasting glucose (mmol/L). 
Adiponectin was assayed with enzyme-linked immunosorbent assay method. The fasting glucose concentration was measured by glucose oxidase-peroxidase (GOD-POD) method,  systolic blood pressure (SBP) and diastolic blood pressure (DBP) were measured twice on the right arm, after a 15-min rest, using a mercury sphygmomanometer.  All protocols were approved by the Institutional Review Board or Ethical Committee (IRB number - XXXIV ECM/P6) at King George's Medical University, Lucknow, Uttar Pradesh, India and all the subjects gave informed consent.
The genomic DNA was extracted from peripheral blood leucocytes pellet using the standard salting-out method.  Single nucleotide polymorphism (SNP) +45T>G in the AMP1 gene was genotyped by the amplification of genomic DNA using the following primers: Forward, 5'- TGT GTG TGT GGG GTC TGT CT-3' and reverse, 5'- TGT GAT GAA AGA GGC CAG AA-3'. The amplification conditions were used as follows: 94°C for 10-min, followed by 35 cycles of 30 s at 94°C, 30 s at 57°C, and 30 s at 72°C, and ending with a single 10-min extension step at 72°C. The polymerase chain reaction fragment was 305-bpin length and was digested with the enzyme Ava I at 37°C. +276G>T in the AMP1 gene was genotyped by the amplification of genomic DNA using another pair of primers: Forward, 5'- CTA CAC TGA TAT AAA CTA TAT GGA G-3' and reverse, 5'- CCC CAA ATC ACT TCA GGT TG-3'. The amplification conditions were as follows: 94°C for 10-min, followed by 35 cycles of 30 s at 94°C, 30 s at 55°C, and 30 s at 72°C, and ending with a single 10-min extension step at 72°C. The resulting fragment was 107 bp in length. The polymorphism was typed using the enzyme Hinf I at 37°C. In the genotyping experiments for both SNPs, the digestion products separated on 15% polyacrylamide gels. Bands were visualized by ethidium bromide staining.
Genotype and allele distribution was compared between obese and nonobese subjects using Chi-square test. The independent segregation of alleles was tested for the Hardy-Weinberg equilibrium, comparing the observed genotype frequencies with those expected (Chi-square test). Haplotype analysis was done by SNP analyzer version 1.2 by expectation-maximization algorithm.  The association of adiponectin concentrations with the genotypes and the haplotypes was estimated using a general linear regression model. Two-tailed tests were performed with the significance level of 0.05. The results for continuous variables are given as the mean ± standard deviation. The differences among three groups were assessed by one-way analysis of variance for continuous variables. Further, we analyzed the change in adiponectin concentrations per copy of one haplotype. A trend per copy of the haplotype with the mean adiponectin concentrations was ascertained in three groups: Subjects with two, one or zero copies of the rare haplotype. All analyses were adjusted for gender, age and BMI.
The association between haplotypes and serum adiponectin concentrations was also evaluated in four subgroups: (1) Nonobese insulin-sensitive (n = 255), (2) nonobese insulin-resistant (n = 78), (3) obese insulin-sensitive (n = 166), (4) obese insulin resistant subjects (n = 143). In a secondary analysis, the parameters SBP and DBP, fasting sugar, adiponectin, FI concentrations, HOMA-IR, T-cholesterol, HDL-C and LDL-C and TGs were tested using a general linear regression model to view their association with the APM1 + 45 and + 276 loci.
| Results|| |
Association of the +45T>G and +276G>T polymorphisms with adiponectin levels
Demographic characteristics of study subjects are summarized in [Table 1]. Levels of adiponectin, insulin, and HOMA-IR index showed significant differences between male and female subjects. SBP and FM also showed a significant difference between both the group while other factors like BMI, fasting blood sugar and lipid profile data did not show any significant sex-specific differences. In [Table 2]a, frequencies of AMP1 genotypes are summarized. The G allele of the APM1 +45 showed a frequency (MAF) of 14.72% while MAF of APM1 +276 was 10.98%. Serum adiponectin level showed highly significant association with both the +45 and the +276 genotypes (P < 0.01 and < 0.01 respectively). After comparing the mean (95% confidence intervals) serum adiponectin concentrations per genotype [Table 2]a], TT genotype (Wild) of +45 AMP1 showed significantly lower adiponectin value than variant genotype GG. Similarly, GG genotype of +276 AMP1 also associated with significantly lower adiponectin value than TT genotypes. A clear trend of decreasing adiponectin levels per copy of the common allele was also observed for +45 SNP P < 0.01, and +276 SNP, P < 0.01).
When APMI haplotypes were constructed, the TG haplotype was the most common, with a frequency of 75.39%. The other significant haplotypes in this sample were the GG (14.02%), TT (9.35%) and the GT (1.24%). The common haplotype TG showed significantly lower adiponectin value than other haplotypes (P < 0.01). The other two haplotypes (GG and TT) with one major and one minor allele were associated with higher adiponectin levels as compared to TG haplotype [Table 2]b]. A clear trend of decreasing adiponectin levels per copy of the common haplotype was observed. All analyses were adjusted for age and sex. Adjustment for age did not show any change in mean adiponectin levels but adjustment for sex did influence the mean values of adiponectin levels.
We divided study subjects in four subgroups: (1) Nonobese insulin-sensitive, (2) nonobese insulin-resistant, (3) obese insulin-sensitive, (4) obese insulin resistant subjects [Table 3]. Nonobese insulin sensitive subjects showed higher adiponectin value (P < 0.01) than nonobese insulin resistant subjects. However, obese insulin sensitive subjects also showed higher adiponectin value (P < 0.01) in comparison with obese insulin resistant subjects. It shows that higher adiponectin levels in both obese and nonobese insulin sensitive subjects. After comparing adiponectin levels in subjects carrying TG haplotype, it emerge that carriers of this haplotypes had lower adiponectin labels both in insulin sensitive and insulin resistant subjects.
The association of the TG haplotype with decreasing adiponectin concentrations was most pronounced in the nonobese insulin-sensitive subjects (P < 0.01 assuming a trend per copy). The association was nonsignificant in the nonobese insulin-resistant subjects, and in the obese insulin-sensitive subjects (P < 0.01 assuming a trend per copy), in the obese insulin-resistant subjects showed significant association (P < 0.01 assuming a trend per copy).
|Table 3: Association of the AMP1 45-276 haplotype and adiponectin concentrations in insulin sensitive categorized subgroups |
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In a secondary analysis, a series of anthropometric and biochemical parameters (T-cholesterol, HDL-C and LDL-C, very low density lipoprotein-cholesterol (VLDL-C), TGs, SBP and DBP, HOMA-IR, fasting glucose and FI concentrations) were analyzed with respect to their association with the TG haplotype [Table 4]. The values of SBP and DBP, adiponectin, insulin, HOMA-IR, T-cholesterol, and LDL-C significantly associated with TG haplotype [Table 4].
|Table 4: Association of clinical and metabolic characteristics of the study population with adiponectin AMP1 45-276 haplotype TG |
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| Discussion|| |
The adipose tissue secretes a variety of molecules having endocrine, paracrine, and autocrine actions and has a role in the etiology of the metabolic abnormalities. Among several proteins secreted by adipocytes, adiponectin is prominent because of its insulin-enhancing actions in the liver and muscle, as well as its anti-inflammatory effects. The present study suggests that two common SNPs, a silent T>G substitution in exon 2 (+45T>G) and a G>T substitution in intron 2 (+276G>T) in AMP1 gene are associated with circulating levels of adiponectin as well as insulin sensitivity.
Previously, there are few studies on the association of AMP1 gene polymorphism with adiponectin levels or insulin resistance. ,,, Gupta et al. observed that AMP1 +45T>G gene polymorphism associated with reduced circulating adiponectin levels in nonalcoholic fatty liver disease patients.  Ong et al. found that genetic variants in the adiponectin gene influenced plasma adiponectin levels in the Chinese population.  Chung et al. observed that subjects with the SNP 45TT genotype showed increased adiponectin levels and AMP1genetic variants can affect insulin resistance indexes.  Youpeng et al. observed significant association of polymorphism +276G>T with serum adiponectin level.  On the other hand, Demirci et al. reported that serum adiponectin levels do not associate with +45T>G gene polymorphism.  Sanghera et al. observed significant association of AMP1 variant with body weight, waist circumference, and hip circumference.  On the other hand, genetic polymorphisms in FTO, and other genes associated with obesity may also contribute to the above association. Systematic testing of these genes is a challenge for any study that follows.
The chromosomal region 3q27, contains APM1, the gene encoding adiponectin. In genome wide linkage scans several susceptibility loci for type 2 diabetes were identified.  Recently, AMP1 gene polymorphism may play an important role in the development of type 2 diabetes in South Indian population.  Stronger associations were observed with the insulin resistance syndrome when the two SNPs were considered together as haplotypes. Menzaghi et al. reported association of the haplotype TG with higher plasma insulin and lower adiponectin levels in healthy individuals.  In the present study, it appears that adiponectin levels are influenced by multiple factors including TG haplotype and obesity phenotype. These finding are also in agreement with a previous study. 
The result showed that, hypoadiponectinemia is a principal, genetically determined defect that contributes into the etiology of obesity and insulin resistance. Adiponectin is significantly associated with obesity, insulin resistance and other obesity-related phenotypes our previous study. 
Animal models studies have reported that adiponectin is a strong insulin enhancer, regulating energy homeostasis and glucose tolerance. , Mice fed a high-fat diet reported weight loss when constantly treated with a proteolytic fragment of adiponectin.  In addition, Insulin resistance decreased in mice after administration of adiponectin, which are genetically predisposed to obesity and diabetes by fatty acid oxidation and by augmenting insulin's ability to reduces hepatic glucose production. , Huang et al. reported that the serum adiponectin level was significantly correlated with HOMA-IR and insulin resistance. 
In the present study insulin and HOMA index showed a significant association with TG haplotype. We found that plasma adiponectin concentrations are associated with insulin sensitivity. Our finding showed that adiponectin concentrations could modulate insulin action by its positive relationship between adiponectin and insulin sensitivity. A dose-dependent effect of adiponectin deficiency on insulin sensitivity observed in heterozygous,  homozygous AMP1 null,  and develop marked diet-induced insulin resistance mice. 
In previous study, plasma adiponectin level was positively associated with insulin sensitivity,  while low concentrations of adiponectin associated with decreased insulin sensitivity in diabetic obese mothers. 
In further analysis to confirm the association among the TG haplotype with insulin sensitivity, we analyzed the impact of the TG haplotype in four subgroups, according to BMI as well as the insulin sensitivity. The association between the serum adiponectin levels and TG haplotype was most prominent in the subgroup of nonobese insulin-sensitive individuals (P < 0.01). This result is supported by a significant relation of the TG haplotype with obesity and insulin resistance. In this context, Melistas et al. reported that insulin resistance associated with the AMP1 +45T>G, +276G>T genotype's in healthy subjects.  In addition, this could also function as physiological factors related to the metabolic syndrome, such as blood levels of FI,  which themselves incline to aggregate in families. 
Other than association of TG haplotype with adiponectin levels, the haplotype is also associated with other features of the insulin resistance syndrome, such as SBP and DBP, insulin level, HOMA-IR and T-cholesterol. The association of circulating adiponectin levels with SNPs 45T>G and 276G>T possibly act through decreased adiponectin expression, which may cause increased body weight and insulin resistance. In a previous study, homozygous/heterozygous carriers of the TG haplotype (45TT and 276GG) showed a significant association with the HOMA-IR index and insulin resistance indexes. 
In the present study, TG haplotype associated with significantly higher value of SBP and DBP. As TG haplotype showed lower value of adiponectin, this low value of adiponectin may responsible for such association. Chow et al. observed that hypoadiponectinemia predicts the development of hypertension and hypertension associated with the APM1 G276T genotype while de Faria et al. reported that hypoadiponectinemia may be a marker for predisposition to hypertension. , A significant negative correlation between adiponectin level and SBP and DBP, in the present and previous study, suggesting that adiponectin contributes to the clinical course of essential hypertension.  The TG haplotype associated with T-cholesterol, and LDL-C. The insulin-sensitizing action of adiponectin in adipose tissue may be responsible for lipid storage insulin signaling in the adipocyte is important while adipose tissue selective insulin receptor knockout mice are protected from obesity. 
| Conclusions|| |
In conclusion, our data show a very strong association of the AMP1 45-276 gene polymorphism and TG haplotypes with adiponectin levels in healthy north Indian population and TG haplotypes also showed substantial association with metabolic parameters of the insulin resistance syndrome.
| Acknowledgements|| |
Authors acknowledge to Indian Council of Medical Research, New Delhi, India for his support to the research (project number - 45/14/2008-HUM-BMS).
| References|| |
Nigro E, Scudiero O, Monaco ML, Palmieri A, Mazzarella G, Costagliola C, et al.
New insight into adiponectin role in obesity and obesity-related diseases. Biomed Res Int 2014;2014:658913.
Arikoglu H, Ozdemir H, Kaya DE, Ipekci SH, Arslan A, Kayis SA, et al.
The adiponectin variants contribute to the genetic background of type 2 diabetes in Turkish population. Gene 2014; 534:10-16.
Marseglia L, Manti S, D'Angelo G, Nicotera A, Parisi E, Di Rosa G, et al.
Oxidative stress in obesity: A critical component in human diseases. Int J Mol Sci 2014;16:378-400.
Francke S, Manraj M, Lacquemant C, Lecoeur C, Leprêtre F, Passa P, et al.
A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27. Hum Mol Genet 2001;10:2751-65.
Xita N, Tsatsoulis A. Adiponectin in diabetes mellitus. Curr Med Chem 2012;19:5451-8.
Yang WS, Lee WJ, Funahashi T, Tanaka S, Matsuzawa Y, Chao CL, et al.
Weight reduction increases plasma levels of an adipose-derived anti-inflammatory protein, adiponectin. J Clin Endocrinol Metab 2001;86:3815-9.
Whitehead JP, Richards AA, Hickman IJ, Macdonald GA, Prins JB. Adiponectin - A key adipokine in the metabolic syndrome. Diabetes Obes Metab 2006;8:264-80.
Zhang C, Luo H, Gao F, Zhang CT, Zhang R. A reduction in both visceral and subcutaneous fats contributes to increased adiponectin by lifestyle intervention in the Diabetes Prevention Program. Acta Diabetol 2014; doi: 10.1007/s00592-014-0655-2.
Kissebah AH, Sonnenberg GE, Myklebust J, Goldstein M, Broman K, James RG, et al.
Quantitative trait loci on chromosomes 3 and 17 influence phenotypes of the metabolic syndrome. Proc Natl Acad Sci U S A 2000;97:14478-83.
Vionnet N, Hani EH, Dupont S, Gallina S, Francke S, Dotte S, et al.
Genomewide search for type 2 diabetes-susceptibility genes in French whites: Evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and independent replication of a type 2-diabetes locus on chromosome 1q21-q24. Am J Hum Genet 2000;67:1470-80.
Li P, Jiang R, Li L, Liu C, Yang F, Qiu Y. Correlation of serum adiponectin and adiponectin gene polymorphism with metabolic syndrome in Chinese adolescents. Eur J Clin Nutr 2015;69:62-7.
Cheung CY, Hui EY, Cheung BM, Woo YC, Xu A, Fong CH, et al.
Adiponectin gene variants and the risk of coronary heart disease: A 16-year longitudinal study. Eur J Endocrinol 2014;171:107-15.
Ramya K, Ayyappa KA, Ghosh S, Mohan V, Radha V. Genetic association of ADIPOQ gene variants with type 2 diabetes, obesity and serum adiponectin levels in south Indian population. Gene 2013;532:253-62.
Daniele A, Cammarata R, Pasanisi F, Finelli C, Salvatori G, Calcagno G, et al.
Molecular analysis of the adiponectin gene in severely obese patients from southern Italy. Ann Nutr Metab 2008;53:155-61.
Lu JF, Zhou Y, Huang GH, Jiang HX, Hu BL, Qin SY. Association of ADIPOQ polymorphisms with obesity risk: A meta-analysis. Hum Immunol 2014;75:1062-8.
Sabouri S, Ghayour-Mobarhan M, Moohebati M, Hassani M, Kassaeian J, Tatari F, et al.
Association between 45T/G polymorphism of adiponectin gene and coronary artery disease in an Iranian population. Scientific World Journal 2011;11:93-101.
El-Shal AS, Zidan HE, Rashad NM. Adiponectin gene polymorphisms in Egyptian type 2 diabetes mellitus patients with and without diabetic nephropathy. Mol Biol Rep 2014;41:2287-98.
Yan CJ, Li SM, Xiao Q, Liu Y, Hou J, Chen AF, et al.
Influence of serum adiponectin level and SNP +45 polymorphism of adiponectin gene on myocardial fibrosis. J Zhejiang Univ Sci B 2013;14:721-8.
Nikolajevic-Starcevic J, Pleskovic A, Santl Letonja M, Jenko Pranikar Z, Petrovic D. Polymorphisms +45T>G and +276G>T of the adiponectin gene does not affect plasma adiponectin level and carotid intima-media thickness in patients with diabetes mellitus type 2. Int Angiol 2014;33:434-40.
Prakash J, Mittal B, Awasthi S, Agarwal CG, Srivastava N. K121Q ENPP1/PC-1 gene polymorphism is associated with insulin resistance in a North Indian population. J Genet 2013;92:571-6.
Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, Turner RC. Homeostasis model assessment: Insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia 1985;28:412-9.
Young DS, Pestaner LC, Gibberman V. Effects of drugs on clinical laboratory tests. Clin Chem 1975;21:1D-432D.
Parker D, Liu K, Dyer AR, Giumetti D, Liao YL, Stamler J. A comparison of the random-zero and standard mercury sphygmomanometers. Hypertension 1988;11:269-72.
Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988;16:1215.
Yoo J, Seo B, Kim Y. SNPAnalyzer: A web-based integrated workbench for single-nucleotide polymorphism analysis. Nucleic Acids Res 2005;33:W483-8.
Mente A, Meyre D, Lanktree MB, Heydarpour M, Davis AD, Miller R, et al.
Causal relationship between adiponectin and metabolic traits: A Mendelian randomization study in a multiethnic population. PLoS One 2013;8:e66808.
Gupta AC, Misra R, Sakhuja P, Singh Y, Basir SF, Sarin SK. Association of adiponectin gene functional polymorphisms (-11377C/G and +45T/G) with nonalcoholic fatty liver disease. Gene 2012;496:63-7.
Ong KL, Li M, Tso AW, Xu A, Cherny SS, Sham PC, et al.
Association of genetic variants in the adiponectin gene with adiponectin level and hypertension in Hong Kong Chinese. Eur J Endocrinol 2010;163:251-7.
Chung HK, Chae JS, Hyun YJ, Paik JK, Kim JY, Jang Y, et al
. Influence of adiponectin gene polymorphisms on adiponectin level and insulin resistance index in response to dietary intervention in overweight-obese patients with impaired fasting glucose or newly diagnosed type 2 diabetes. Diabetes Care 2009;32:552-8.
Youpeng B, Wei X, Wei L, Jin J, Haiyan Y, Yuan Y, et al.
Relationships among adiponectin gene polymorphisms, proteinuria and increased blood pressure in the context of placental diseases. Hypertens Res 2010;33:1066-70.
Demirci H, Yilmaz M, Ergun MA, Yurtcu E, Bukan N, Ayvaz G. Frequency of adiponectin gene polymorphisms in polycystic ovary syndrome and the association with serum adiponectin, androgen levels, insulin resistance and clinical parameters. Gynecol Endocrinol 2010;26:348-55.
Sanghera DK, Demirci FY, Been L, Ortega L, Ralhan S, Wander GS, et al.
PPARG and ADIPOQ gene polymorphisms increase type 2 diabetes mellitus risk in Asian Indian Sikhs: Pro12Ala still remains as the strongest predictor. Metabolism 2010;59:492-501.
Prakash J, Srivastava N, Awasthi S, Agarwal CG, Natu SM, Rajpal N, et al.
Association of FTO rs17817449 SNP with obesity and associated physiological parameters in a north Indian population. Ann Hum Biol 2011;38:760-3.
Livshits G, Malkin I, Moayyeri A, Spector TD, Hammond CJ. Association of FTO gene variants with body composition in UK twins. Ann Hum Genet 2012;76:333-41.
Malhotra A, Igo RP Jr, Thameem F, Kao WH, Abboud HE, Adler SG, et al.
Genome-wide linkage scans for type 2 diabetes mellitus in four ethnically diverse populations-significant evidence for linkage on chromosome 4q in African Americans: The Family Investigation of Nephropathy and Diabetes Research Group. Diabetes Metab Res Rev 2009;25:740-7.
Biswas D, Vettriselvi V, Choudhury J, Jothimalar R. Adiponectin gene polymorphism and its association with type 2 diabetes mellitus. Indian J Clin Biochem 2011;26:172-7.
Menzaghi C, Ercolino T, Di Paola R, Berg AH, Warram JH, Scherer PE, et al.
A haplotype at the adiponectin locus is associated with obesity and other features of the insulin resistance syndrome. Diabetes 2002;51:2306-12.
Mackevics V, Heid IM, Wagner SA, Cip P, Doppelmayr H, Lejnieks A, et al.
The adiponectin gene is associated with adiponectin levels but not with characteristics of the insulin resistance syndrome in healthy Caucasians. Eur J Hum Genet 2006;14:349-56.
Prakash J, Mittal B, Awasthi S, Agarwal CG, Srivastava N. Hypoadiponectinemia in obesity: Association with insulin resistance. Indian J Clin Biochem 2013;28:158-63.
Huang Y, Li Y, Chen Q, Chen H, Ma H, Su Z, et al.
Low serum adiponectin levels are associated with reduced insulin sensitivity and lipid disturbances in short children born small for gestational age. Clin Endocrinol (Oxf) 2014. doi: 10.1111/cen.12663.
Kubota N, Terauchi Y, Yamauchi T, Kubota T, Moroi M, Matsui J, et al.
Disruption of adiponectin causes insulin resistance and neointimal formation. J Biol Chem 2002;277:25863-6.
Yamamoto Y, Hirose H, Saito I, Tomita M, Taniyama M, Matsubara K, et al.
Correlation of the adipocyte-derived protein adiponectin with insulin resistance index and serum high-density lipoprotein-cholesterol, independent of body mass index, in the Japanese population. Clin Sci (Lond) 2002;103:137-42.
Maeda N, Shimomura I, Kishida K, Nishizawa H, Matsuda M, Nagaretani H, et al.
Diet-induced insulin resistance in mice lacking adiponectin/ACRP30. Nat Med 2002;8:731-7.
Ramirez VI, Miller E, Meireles CL, Gelfond J, Krummel DA, Powell TL. Adiponectin and IGFBP-1 in the development of gestational diabetes in obese mothers. BMJ Open Diabetes Res Care 2014;2:e000010.
Melistas L, Mantzoros CS, Kontogianni M, Antonopoulou S, Ordovas JM, Yiannakouris N. Association of the +45T>G and +276G>T polymorphisms in the adiponectin gene with insulin resistance in nondiabetic Greek women. Eur J Endocrinol 2009;161:845-52.
Gaens KH, Goossens GH, Niessen PM, van Greevenbroek MM, van der Kallen CJ, Niessen HW, et al.
Ne-(carboxymethyl) lysine-receptor for advanced glycation end product axis is a key modulator of obesity-induced dysregulation of adipokine expression and insulin resistance. Arterioscler Thromb Vasc Biol 2014;34:1199-208.
Prakash J, Srivastava N, Awasthi S, Agarwal C, Natu S, Rajpal N, et al.
Association of PPAR-g gene polymorphisms with obesity and obesity-associated phenotypes in North Indian population. Am J Hum Biol 2012;24:454-9.
Chow WS, Cheung BM, Tso AW, Xu A, Wat NM, Fong CH, et al.
Hypoadiponectinemia as a predictor for the development of hypertension: A 5-year prospective study. Hypertension 2007;49:1455-61.
de Faria AP, Demacq C, Figueiredo VN, Moraes CH, Santos RC, Sabbatini AR, et al.
Hypoadiponectinemia and aldosterone excess are associated with lack of blood pressure control in subjects with resistant hypertension. Hypertens Res 2013;36:1067-72.
Imatoh T, Miyazaki M, Momose Y, Tanihara S, Une H. Adiponectin levels associated with the development of hypertension: A prospective study. Hypertens Res 2008;31:229-33.
Blüher M, Michael MD, Peroni OD, Ueki K, Carter N, Kahn BB, et al.
Adipose tissue selective insulin receptor knockout protects against obesity and obesity-related glucose intolerance. Dev Cell 2002;3:25-38.
[Table 1], [Table 2], [Table 3], [Table 4]
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