Genetic Identification for Non-Communicable Disease: Findings from 20 Years of the Tehran Lipid and Glucose Study

Maryam S Daneshpour; Mehdi Hedayati; Bahareh Sedaghati-Khayat; Kamran  Guity; Maryam  Zarkesh; Mahdi  Akbarzadeh; Niloofar  Javanrooh; Azita  Zadeh-Vakili; Fereidoun  Azizi

doi:10.5812/ijem.84744

Genetic Identification for Non-Communicable Disease: Findings from 20 Years of the Tehran Lipid and Glucose Study

authors:

Maryam S Daneshpour ¹ , avatar Mehdi Hedayati ¹ , Bahareh Sedaghati-Khayat ¹ , Kamran Guity ¹ , Maryam Zarkesh ¹ , Mahdi Akbarzadeh ¹ , Niloofar Javanrooh ¹ , Azita Zadeh-Vakili ¹ , Fereidoun Azizi ^{2
, *}

1 Cellular and Molecular Endocrine Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran

2 Endocrine Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran

International Journal of Endocrinology and Metabolism: Vol.16, issue 4 (Suppl); e84744

published online: October 27, 2018

article type: Review Article

received: September 1, 2018

revised: October 2, 2018

accepted: October 9, 2018

DOI: https://doi.org/10.5812/ijem.84744

how to cite: Daneshpour M S, Hedayati M, Sedaghati-Khayat B, Guity K , Zarkesh M , et al. Genetic Identification for Non-Communicable Disease: Findings from 20 Years of the Tehran Lipid and Glucose Study. Int J Endocrinol Metab. 2018;16(4 (Suppl)):e84744. https://doi.org/10.5812/ijem.84744.

Abstract

Context:

Tehran Lipid and Glucose Study (TLGS), a longitudinal family based cohort study, is the oldest and largest longitudinal family based study in Iran, aimed at investigating effects of environmental, social and biological factors on the health of Tehranians over time. Considering the importance of genetic studies in this aspect, here we present a summary of the important genetic findings, and the potentiality of their contributions to future related projects.

Evidence Acquisition:

For all related studies during the past 20 years the search sources were all prominent search engines such as PubMed, Scopus, and Google Scholar with the most proper Medical Subject Headings (MeSH).

Results:

This review summarizes associations of 6 binary phenotypes and 17 quantitative traits with genetic markers in 26 genes. Of the 47 genetic markers, studied most were related to cardio metabolic risk factors. Results of heritability and linkage analysis were also collected and the highest heritability was found to be related to HDL-C (0.5).

Conclusion:

Considering the opportunity provided by large-scale cohort studies to investigate molecular effects of genetic variants on causality and different omics’ data, genetic studies conducted on TLGS population have had a remarkable success in identifying genetic variants that facilitating a unique genetic database on Iranian populations. The results of genome wide association studies in this population are currently facilitating investigations to define the Iranian genetic differences with other population.

Keywords

Tehran Lipid and Glucose Study Tehran Cardio-Metabolic Genetic Study Genetic Association Heritability

1. Context

Research of common diseases, currently uses analysis of genetic data available on the functioning of human genome, as the primary most reliable tool for determination of new variants of this genome (1). In addition to genetic variants, environmental and behavioral changes also play an important role in the development of chronic diseases. Therefore, in association studies, gene-environment interactions or presence of a particular environmental exposure, are being strongly emphasized (2). In some situations, populations are related to a lot of exposures in different ways which cause to adjust the effect of specific genetic variants; the resulting interactions can prevent the detection of a genetic effect (3). Collection of pre-morbid exposure can be allowed to standardize by the prospective cohort design. Identifying genomic variations in participants improves the power of these studies. Assessment of environmental risk factors and analyzing gene-environment interactions would provide solid data, less prone to bias and easily extrapolatable to the entire population, compared to case-control studies.

This review highlights some of the important findings documented on genetic cardio metabolic risk factors investigated in the Tehran Lipid and Glucose Study (TLGS) over twenty years.

2. Evidence Acquisition

The search sources for covering a complete range studies were all prominent search engines such as PubMed, Scopus, and Google Scholar with the most proper Medical Subject Headings (MeSH) during the past 20 years.

3. Results

3.1. Project Description

TLGS is a prospective ongoing family based cohort study, conducted on over 15,000 individuals, aged 3 years, enrolled in Phase 1 and followed every 3.5 years since 1999 (4). Other individuals from different pedigrees were also added to the cohort during the follow-up period. Hence, after 20 years of follow-up (2017), 23259 individuals of 5434 households had participated in the study (5). At each visit, subjects signed a consent form and were interviewed to document demographic data including marriage status and spouse information, and were then referred to trained physicians for clinical examinations of the anthropometric and cardiovascular risk factors; they were also referred to laboratories for blood sampling for extraction of sera and DNA. Composition and familial relationship have been described elsewhere (5).

3.2. Heritability and Aggregation

In the present project, the heritability of metabolic syndrome, obesity and lipid profiles of TLGS families were estimated after age and sex adjustment (Table 1) (6, 7). The highest heritability was for HDL-C (about 50%) and the lowest was for metabolic syndrome (15%). Metabolic syndrome components were investigated using exploratory factor analysis (EFA) and results showed that three important factors, including blood pressure, lipids, and obesity in conjunction with fasting blood sugar are the sub components of the metabolic syndrome with heritability of around 6.14 and 7%, respectively (7).

Table 1.

Estimated Heritability for Studied TLGS Phenotypes

Cardiometabolic Risk Factors	Mean Heritability^a, %	P Value
Lipids
HDL-C	0.5	8.7 × 10^-129
TG	0.36	1.1 × 10^-36
FBS	0.29	Less than 0.05
SBP	0.25	Less than 0.05
DBP	0.26	Less than 0.05
LDL	0.33	4.2 × 10^-64
Total cholesterol	0.32	1.8 × 10^-61
Non-HDL-C	0.3	1.9 × 10^-55
Obesity
BMI	0.3	7.3 × 10^-19
WC	0.27	Less than 0.05
WHR	0.27	8.0 × 10^-17
Waist circumference	0.32	9.1 × 10^-22
REE	0.26	4.6 × 10^-12
Hip	0.21	1.6 × 10^-10
Height	0.23	2.4 × 10^-13
Weight	0.33	6.9 × 10^-24
Body size	0.51	5.9 × 10^-47
High BMI	0.57	5.8 × 10^-6
Abdominal obesity	0.48	1.1 × 10^-13
High WHR	0.33	0.1 × 10^-6
Metabolic syndrome
Metabolic syndrome score	0.15	Less than 0.05

Abbreviations: HDL-C, high density lipoprotein; TG, triglycerides; FBS, fasting blood sugar; SBP, systolic blood pressure; DBP, diastolic blood pressure; LDL, low density lipoprotein; BMI, body mass index; WC, waist circumference; WHR, waist to hip ratio; REE, resting energy expenditure.

^aHeritability estimation adjusted for age and sex.

Moreover, familial aggregation of the metabolic syndrome components was studied unmarried adolescents who had at least one parent with available information. Results showed a strong correlation between risk of metabolic syndrome in children and parents and significant differences in means of triglycerides, HDL-C and body mass index between children of parents with metabolic syndrome and those whose parents were metabolic syndrome free (8).

3.3. Genetic Association Studies

Genetic association studies, powerful tools used in investigating the correlation between disease status and genetic variation, are helpful in identifying candidate genes or genomic regions that contribute to a specific complex disorder (9). Usually, the candidate genomic regions for different studies are selected based on the results of previous studies, especially previous genome wide association studies conducted on the same population or on other similar populations. Here, we described the most important genetic findings of studies conducted on TLGS participants since 1999.

3.4. Lipid Metabolism

Low HDL-C concentration is the most frequent lipid related risk factor in Iran (10). Some missense mutations in ABCA1 (ATP binding cassette subfamily a member 1), APOA1 (apolipoprotein A1), APOE (apolipoprotein E), APOA5 (apolipoprotein A5), and SCARB1 (scavenger receptor B1) showed significant associations with decrease of HDL-C (11-18); other HDL-C related variations were observed in the splice site, intronic, upstream and downstream regions. The most studied intronic variations in the CETP gene in different populations are rs753562256 (TaqI) and rs708272 (-629A/C) (19). In TLGS participants, allele frequencies were 0.382 for the Taql B2 and 0.462 for the -629A/C A. In addition, linkage disequilibrium analysis showed that Taql B1 and B2 alleles and the alleles of the-629A/C variant were in linkage disequilibrium in our population (D = 0.0965 and 0.4695, respectively). There was a significant association between the presence of B2 and A alleles with higher HDL-C concentration and low CETP activity (20, 21).

In 2012, the effects of two polymorphisms, rs63750792 and rs2070665 were studied in the TLGS population and significant associations were found between triglyceride, HDL-C, HDL₂, and levels of Apo AI and Apo B (14). Some years later, Bandarian et al. in an exon and promoter sequence analysis conducted among 63 individuals according to 95th percentile of HDL-C (extremely high) on apolipoprotein A1; their sequencing results showed 42 common and rare variants. Exonic variants included eleven missense, six synonymous, and one nonsense (13).

Regarding the huge effect of the APO gene cluster on lipid profile measurements and the large number of genes in this family, XbaI Apo lipoprotein B polymorphisms were found to have a significant association with increased total cholesterol and Apo lipoprotein B in a cross-sectional study of 849 TLGS participants, associations that remained significant even after adjusting for demographic and blood covariates i.e., age, sex, body mass index, smoking, diastolic and systolic blood pressure, and fasting blood sugar (22).

Mutations in the LDL-R (low density lipoprotein receptor) gene could lead to autosomal dominant disorder, familial hypercholesterolemia. In this gene, the splice region variant rs72658867-A and rs17248748-T in intron 14 and intron 1 are associated with lower non-HDL-C levels and confer protection against CAD. Retention of intron 14 during transcription is caused by the LDLR splice region variant, rs72658867-A, located at position +5 in intron 14 (NM-000527: c.2140 + 5G > A) and can appear a truncated LDL receptor lead to mainly lacked functions of the receptor. This retention of the intron characterizes almost half of the transcripts generated from chromosomes carrying rs72658867-A. Also, in spite of the wild type transcripts do not exceed levels in non-carriers the same variant increases LDLR mRNA expression and this demonstrated that the sequence variants disrupt the LDL receptor can lower non-HDL-C and protect against CAD (23).

One of the well-known variations related to HDL-C concentration is rs1800588 (-514C/T), which may influence HDL-C (24); generally, the (T) allele is considered to lead to higher HDL-C levels. The “T” allele non-carriers in the -514C/T polymorphism of the LIPC gene have lower level of HDL-C than carriers.

SRBI or SCARB1 (scavenger receptor class B member 1) is a key component in reverse cholesterol transportation. In a study conducted to assess the association between lipid profiles and rs4238001 polymorphism through the SR-BI gene among the TLGS residents, minor allele frequency of the polymorphism of SR-BI gene was 0.159 (18); in addition, the association of rs4238001 with HDL-C and HDL-3 was not significant except after adjusting for age. The result of this study showed that age has a confounder role which could regulate the strength of association between the single nucleotide polymorphism of SR-BI and HDL-C level trait (18).

Relationships of the LCAT (lecithin-cholesterol acyltransferase) gene with lipid profiles have also been investigated. Through this study, the promoter, coding regions and exon/intron boundaries of LCAT were amplified. As a result, sequenced in consecutive individuals (n = 150) who had hardly low or high HDL-C levels with no other major lipid abnormalities; 14 single-nucleotide polymorphisms (SNPs) were determined included 10 novel SNPs. Three of the novel variations (position 5,151 in exon 1, position 6,531 in exon 5, and position 6,696 in exon 5) are caused by an amino acid substitution. However, results did not show very strong associations between recognized variants and HDL-C (25). Also, a replicate study conducted on rs5923 polymorphism of the LCAT gene showed no associations with low HDL-C levels in an Iranian population (26).

3.5. Metabolic Syndrome

Genetic studies of the metabolic syndrome in the TLGS, use one of the three following definitions: (1) “National Cholesterol Education Program Adult Treatment Panel III (ATP III)” (27), (2) International Diabetes Federation (IDF) (28) and (3) The Joint Interim Statement (JIS) (29). Furthermore, based on national reports, Azizi et al. suggested a waist circumference cutoff ≥ 95 cm for those aged above 16 years, and WC > 78 cm for those aged between 10 - 16 year (30).

Association studies of genetic markers in the APO gene cluster regions with dietary patterns conducted on patients with metabolic syndrome showed that the rs5128 is associated with different nutrient components in metabolic syndrome affected individuals (31, 32).

Moreover, the relation of variation rs5110 (G360T) with metabolic syndrome has been evaluated in a case/control study (16). Results showed that APOA5 rs2075291 could play an important role in triglyceride and HDL-C levels in individuals affected with metabolic syndrome, although the association of APOA5 rs662799 polymorphism with these levels is still under debate (33).

CD36 (CD36 Molecule), MC4R (melanocortin 4 receptor), and SLC30A8 (solute carrier family 30 member 8 (ZnT-8)) are other important genes that have been reported to be associated with metabolic syndrome in TLGS families (34).

3.6. Obesity

CVD risk factors of obesity have a high heritability as shown in Table 1. Many loci have been reported to be associated with obesity risk factors worldwide. Obesity related genetic regions focused on the effect of the 16q12.2 region, which contains the FTO (fat mass and obesity-associated protein), IRX (iroquois-class homeodomain protein), and MMP (matrix metallopeptidase) family genes, FABP2 (fatty acid binding protein 2), ADRB3 (adrenoceptor beta 3), IL6 (interleukin 6), PPAR-γ (peroxisome proliferator-activated receptor gamma), TNF (tumor necrosis factor-alpha), and CCND2 (cyclin D2) genes.

The chromosomal region 16q12.2 contains the most obesity related genes. Various GWA and Meta GWA have provided clear evidences confirmed that FTO is associated with body mass index, and affects dietary intakes and preferences for certain energy-dense foods, as well (35) (Figure 1). In a study conducted on 6928 unrelated subjects with 986 genotyped SNPs located on the 16q12.2 regions, significant SNP sets were relatively denser in the introns of FTO, AIKTIP, and MMP2 genes and near IRX3 gene (Figure 1) (35). Although previous studies confirm the association between rs1421085, rs1121980, rs1558902, and rs8050136 in the first intron of the FTO gene and body mass index, this review showed no association between FTO variants and body mass index in healthy metabolic obese (HMO) individuals (36). FABP2 genes are thought to play a role in the intracellular transport of long-chain fatty acids and their Acyl-CoA esters and may help in maintaining energy homeostasis by functioning as a lipid sensor. Examining a missense variant (rs1799883) on the FABP2 gene among individuals with body mass index ≥ 30 Kg/m² showed no significant differences between case and control groups in terms of allele frequency (37).

Figure 1.

Regional association plot shows the P values (-log P values) of each SNP and recombination rate in the 16q12.2 region. The red line is related to -Log (0.05), indicating significance level. For each significant set, SNP with the lowest P value is determined (35).

In the ADRB3 gene, an association was found between variations in rs4994 and obesity in TLGS population (38). A case-control study examining the relation of rs1801282 polymorphism in the PPAR-γ gene with obesity in 479 participants the TLGS indicated that the presence of G allele could lead to a 1.7 fold increase in the risk of obesity (39).

Regarding previous studies, elevated TNFα levels are linked to obesity and insulin resistance in some populations; the association of obesity with rs1800629 and rs361525 (in the promotor region) was investigated in an adult Iranian population and results showed that these SNPs were not an important risk factor for obesity or consequently for cardiovascular disease (40).

CCND2 encodes a G1/S cell cycle regulator and is the key regulator of postnatal pancreatic β cell mass (41). This cyclin forms a complex with CDK4 or CDK6 and functions as a regulatory subunit of the complex, whose activity is required for cell cycle G1/S transition. In the TLGS population, a variant with low frequency of 1.47% in intron 1 of CCND2 gene, rs76895963, showed significant associations with both increased height and body mass index showed significant associations with both increased height (1.17 cm per allele, P = 5.5 × 10^-12) and body mass index (0.56 kg/m² per allele, P = 6.5 × 10^-7). Moreover, the G allele of this variant reduces risk of type II diabetes by 50% (odds ratio (OR) = 0.53 (P = 5.0 × 10^-21)) (42).

3.7. Diabetes

In accordance with the definition provided by the American Diabetes Association, adult participants are considered to have diabetes if they meet at least one of the following criteria: FPG ≥ 126 mg/dL, or 2h-PCPG ≥ 200 mg/dL or taking anti-diabetic medication (43). In addition to TCF7L2 (transcription factor 7 like 2) and HHEX, which encode for proteins implicated in blood glucose homeostasis, the effects of PDX1 (pancreatic and duodenal home box 1) and PAM (pancreatic and duodenal homeobox1) genes on type II diabetes (T2D) in TLGS families were investigated.

The PAM gene encodes a multifunctional protein; two missense variants in this gene carrying p.Asp563Gly (with frequency of 4.98% and OR = 1.23, P = 3.9 × 10^-10) and p.Ser539Trp (with frequency of 0.65%, OR = 1.47, P = 1.7 × 10^-5), allow moderately higher risk of T2D (42).

A transcriptional activator of several genes account for insulin, somatostatin, glucokinase, islet amyloid polypeptide, and glucose transporter type 2 is encoded a protein by PDX1. In our population a rare (0.20%) frameshift variant in PDX1, carrying p.Gly218Alafs*12, demonstrated an association with high risk of T2D (OR = 2.27, P = 7.3 × 10^-7) (42).

3.8. Thyroid

Previous studies confirm our findings on the association between TPO (thyroid peroxidase) gene polymorphisms with both anti-TPO and anti-TG factors. TPO or iodide peroxidase is a key enzyme expressed in the thyroid for hormone foundation. TPO catalyzes oxidation of iodide ions to iodine atoms that form iodothyronines in a thyroglobulin (Tg) molecule for the production of thyroxine (T4) or triiodothyronine (T3) hormones (44). Serum autoantibodies in patients with Graves’ disease or Hashimoto’s thyroiditis recognized the TPO that is the major thyroid autoantigen (45). The TPO is a membrane-bound glycoprotein and which in humans, consists of 933 amino acids that are encoded by the mRNA of 3048 nucleotides. The TPO gene consists of 17 exons and extends over 150 kb on the short arm of chromosome 2, locus 2p25. According to molecular genetic studies, mutations in this gene are associated with one of the most common causes of autoimmune thyroid diseases i.e. autosomal recessive inheritance (46, 47). Autoimmune thyroid diseases result from the interaction of several mechanisms, including total absence of TPO activity, inability of TPO to bind to the hem cofactor, inability to interact with the Tg substrate, and abnormal sub cellular localization, all of which are affected by various mutations in the TPO gene. Of TPO gene variations, the associations of C2145T (rs732608), G1193C (rs2175977), and A1936G (rs10189135) polymorphisms with anti-TPO levels were evaluated in the TLGS population. Results showed that the C allele polymorphism in the synonymous variant C2145T of exon 12 is associated with high levels of serum anti-TPO and that carriers of this allele are predisposed to autoimmune thyroid disease 9.2 fold higher than those, who have no C allele. Moreover, missense variant G1193C of exon 8 has no effect on increased levels of anti-TPO (48), although, in the missense variant A1936G of exon 11, the G allele is significantly associated with increased anti-TPO levels (49); all the above results suggest that the rs732608 and rs10189135 polymorphisms are associated with high levels of anti-TPO in this population (49).

3.9. Polycystic Ovary Syndrome (PCOS)

The most prevalent endocrinopathy in female is PCOS. This disorder affects 6% - 10% of caucasian premenopausal women (50), with a reported prevalence of 7% among Iranian women, based on the NIH definition (51).

Associations between PCOS and variations in three different genes, TCF7L2, HHEX, and VDR (vitamin D receptor) have been investigated. TCF and HHEX genes have been implicated in blood glucose homeostasis and genetic variants of this gene are associated with increased risk of T2D. Given the simultaneous occurrence of PCOS and T2D (indicating a common underlying genetic etiology) (52), the association between IR and two strongly T2D associated gene variants (rs7903146 in TCF7L2, and rs1111875 in HHEX) is affected by PCOS status in Iranian women. After adjustment for age and body mass index, a protective effect of the HHEX A allele is observed on the risk of IR in non-PCOS subjects (confidence interval (95%): 0.33 - 0.78; P = 0.002) (52).

The VDR gene encodes the nuclear hormone receptor for vitamin D3. A single nucleotide polymorphism rs757343 in the initiation codon were studied (53-55) and the results showed that presence of the A allele was associated with a 74% increased risk of severe phenotype development (OR, 1.74; 95% CI, 1.07 - 2.82) while no association was observed with disease risk.

3.10. Hip Osteoarthritis and CHADL Gene Variant

The CHADL (chondroadherin like) in the 22q13.2 region is a negative modulator of the chondrocyte differentiation. In an Iranian population the allele frequency of a frameshift mutation, rs532464664 (p. Val330Glyfs*106) was 0.0115 and 23 of the studied individuals were heterozygous for this variation (56).

3.11. Tehran Cardio Metabolic Genetic Study (TCGS)

Considering the importance of genome wide association studies, exome sequencing and whole genome analyses, TCGS was designed in collaboration with the Research Institute for Endocrine Sciences (RIES) and the deCODE genetics company. The TCGS cohort comprises 17,186 (86.3%) of the 19,905 TLGS participants who provided baseline blood samples for plasma and DNA analysis. This study comprises of 849 independent individuals and 3109 families with at least one member with complete genotype data. Studies took account into the TCGS have been being navigated to determine relevant specimen of genetic polymorphisms that could be associated to cardio-metabolic risk factors in Tehran. TLGS database, the oldest and biggest Iran cohort, includes clinical, behavioral, and biochemical data for the whole participants. After augmenting this study by starting TCGS project and appending genome-wide data to the TCGS database, the study would be capable to consider gene-gene and gene-environment interactions and their relation to disease status (5).

4. Conclusions

Iran is a large country with diverse ethnicities, with a high rate of consanguineous marriage in some regions resulting in high inbreeding rates and different ethnicities and complex genetic pattern for this population. Considering that, Tehran, the capital city of Iran, has diverse ethnicities and cultures, the TLGS population could provide us with valuable information on Iranian populations. Since, these individuals have been followed for at least 20 years, their phenotype and genotype variations, in addition to their outcomes provide us with good infrastructure for research, the findings of which could shed more light on non-communicable disorders. A summary of genetic association studies has been shown in Table 2 and Figure 2A and 2B. Totally 48 variations in 26 genes in relation to the phenotypes were studied in the TLGS. Among them, 34% of studied variants were in coding consequences, and 20 of them were missense variants. Currently, all participants of the TCGS are chip-typed and over 1000 individuals have been genome sequenced. Data of the TLGS and related studies not only add to current knowledge on genomic differences between Iranian populations and other countries but also recommend new strategies for early prevention and treatment of non-communicable diseases. Moreover, results of the TLGS delineate the path to personalized medicine and predictive medicine, which benefit both individuals and governments providing cost-effective treatments and increasing the quality of life especially in elderly patients.

Table 2.

Studied Polymorphisms in TLGS

Symbols	SNP	Location (Allele)	Consequence	Codons (Amino acids)	Studied Phenotypes/Traits	Sample Size	References
ABCA1	rs2230806	9: 104858586 (T)	Missense	aGg/aAg (R/K)	Cholesterol, triglyceride, HDL-C, apolipoprotein A1, apolipoprotein B	823, 778	(11)
ADRB3	rs4994	8: 37966280 (G)	Missense	Tgg/Cgg (W/R)	Obesity, BMI	401	(38)
APOA1
	rs2070665	11: 116836968 (G)	Downstream	-	Extreme high and low HDL	132	(12, 13)
	rs121912724	11: 116836361 (C)	Missense	cTg/cGg (L/R)	Extreme high and low HDL	132	(12, 13)
	rs201148448	11: 116837080 (A)	Missense	Gtg/Ttg (V/L)	Extreme high and low HDL	132	(12, 13)
APOA2
	rs6413453	1: 161222526 (A)	Splice region, Intron	-	Extreme high and low HDL	132	(12, 13)
	rs5069	11: 116837538 (A)	Intron	-	Cholesterol, triglyceride, HDL-C, apolipoprotein A1, dietary pattern	823, 828	(32, 57)
	rs670	11: 116837697 (T)	5-prime-UTR	-	Cholesterol, triglyceride, HDL-C, apolipoprotein A1, dietary pattern	823, 828	(32, 57)
	rs5082	1: 161223893 (A)	Upstream	-	Extreme high and low HDL	132	(12, 13)
APOA3	rs5128	11: 116832924 (C)	Downstream	-	Cholesterol, triglycerides, HDL-C, apolipoprotein A1, Dietary fatty acids, dietary pattern, metabolic syndrome	823, 1510, 828	(32)
APOA5
	rs662799	11: 116792991 (A)	Upstream	-	Metabolic syndrome, HDL-C	947	(16, 58)
	rs2075291	11: 116790676 (A)	Missense	Ggc/Tgc (G/C)	Metabolic syndrome, HDL-C	947	(16, 58)
	rs3135506	11: 116791691 (A)	Missense	tCg/tTg (S/L)	Metabolic syndrome, HDL-C	947	(16, 58)
APOB	rs693	2: 21009323 (A)	Synonymous	acC/acT (T)	Cholesterol, triglyceride, HDL-C, apolipoprotein B	849	(14)
APOE
	rs7412	19: 44908822 (T)	Missense	Cgc/Tgc (R/C)	HDL-C, LDL-C, obesity, BMI	1030, 843	(17, 59)
	rs429358	19: 44908684 (C)	Missense	Tgc/Cgc (C/R)	HDL-C, LDL-C, obesity, BMI	1030, 843	(17, 59)
CCND2	rs76895963	12: 4275678 (G)	intron	-	Diabetes, height, BMI	1,624 cases, 9,163 controls	(42)
CD36
	rs10499859	7: 80629494 (G)	Intron	-	Metabolic syndrome, HDL-C	337	(34, 60)
	rs13246513	7: 80677435 (G)	Downstream	-	Metabolic syndrome, HDL-C	337	(34, 60)
CETP
	rs708272	16: 56962376 (A)	intron	-	Cholesterol, triglycerides, HDL-C	1021, 555	(20, 21)
	rs1864163	16: 56963321 (A)	Intron	-	Cholesterol, triglycerides, HDL	1021, 555	(20, 21)
CHADL	rs532464664	22: 41238083 (insCGCGCGCC)	Frameshift mutation	gtg/gGGCGCGCGtg (V/GRAX)	Hip osteoarthritis	996	(56)
FABP2	rs1799883	4: 119320747 (A)	Missense	Act/Tct (T/S)	Obesity, BMI	400	(61)
FTO
	rs1421085	16: 53767042	Intron	-	BMI, MUHO	945	(62)
	rs1558902	16: 53769662	Intron	-	BMI, MUHO	945	(62)
	rs1121980	16: 53775335	Intron	-	BMI, MUHO	945	(62)
	rs8050136	16: 53782363	Intron	-	BMI, MUHO	945	(62)
HHEX	rs1111875	10: 92703125 (T)	Intergenic	-	PCOS	504	(52)
IL6	rs1800795	7: 22727026 (G)	Intron	-	Obesity, BMI	214	(63)
LCAT	rs5923	16: 67940050 (A)	Synonymous	Ctg/Ttg (L)	HDL-C	130	(64)
LDLR
	rs200238879	19: 11105602 (C)	Splice region, intron	-	Non-HDL, triglycerides, HDL-C	9,631	(23)
	rs17248720	19: 11087511 (T)	Upstream	-	Non-HDL, triglycerides, HDL-C	9,631	(23)
	rs17248748	19: 11095364 (T)	Intron	-	Non-HDL, triglycerides, HDL-C	9,631	(23)
	rs72658867	19: 11120527 (A)	Splice region, intron	-	Non-HDL, triglycerides, HDL-C	9,631	(23)
LIPC	rs1800588	15: 58431476 (T)	Upstream	-	Cholesterol, triglycerides, HDL-C	1021, 555	(65)
MC4R	rs12970134	18: 60217517 (A)	Intergenic	-	Dietary pattern, metabolic syndrome	815	(66, 67)
PAM
	rs35658696	5: 103003107 (G)	Missense variant	gAt/gGt (D/G)	Diabetes	1,624 cases, 9,163 controls	(42)
	rs760687925	1: 204973276 (G)	Missense, splice region	tCg/tGg (S/W)	Diabetes	1,624 cases, 9,163 controls	(42)
PPAR-γ	rs1801282	3: 12351626 (G)	Missense	Cca/Gca (P/A)	Obesity, BMI	239
SCARB1	rs4238001	12: 124863717 (T)	Missense	Ggc/Agc (G/S)	Cholesterol, triglycerides, HDL	774
SLC30A8	rs13266634	8: 117172544 (T)	Missense	Cgg/Tgg (R/W)	Dietary patterns	816 case and 816 control
TCF7L2	rs7903146	10: 112998590 (T)	Intron	-	Diabetes	11000
TNF
	rs1800629	6: 31575254 (A)	Upstream	-	Obesity, BMI	244
	rs361525	6: 31575324 (A)	Upstream	-	Obesity, BMI	244
TPO
	rs732608	2: 1496127 (C > T)	Synonymous variant	(Pro715)	Weight, Anti- TPO, Anti-Tg	184
	rs2175977	2: 1477459 (G > C)	Missense variant	(S/T)	Weight, Anti- TPO, Anti-Tg	184
	rs10189135	2: 1493885 (A > G)	Missense variant	(V/M)	Anti TPO, weight	190
VDR
	rs757343	12: 47845892 (T)	Intron	-	PCOS	260
	rs1544410	12: 47846052 (T)	Intron	-	PCOS	260

Figure 2.

A, All genetic variation consequences studied in TLGS; B, coding consequences studied in TLGS (35)

Acknowledgements

References

1.
Manolio TA, Bailey-Wilson JE, Collins FS. Genes, environment and the value of prospective cohort studies. Nat Rev Genet. 2006;7(10):812-20. [PubMed ID: 16983377]. https://doi.org/10.1038/nrg1919.
2.
Hunter DJ. Gene-environment interactions in human diseases. Nat Rev Genet. 2005;6(4):287-98. [PubMed ID: 15803198]. https://doi.org/10.1038/nrg1578.
3.
Polito L, Greco A, Seripa D. Genetic profile, environmental exposure, and their interaction in parkinson's disease. Parkinsons Dis. 2016;2016:6465793. [PubMed ID: 26942037]. [PubMed Central ID: PMC4752982]. https://doi.org/10.1155/2016/6465793.
4.
Azizi F, Madjid M, Rahmani M, Emami H, Mirmiran P, Hadjipour R. [Tehran lipid and glucose study (TLGS): Rationale and design]. Iran J Endocrinoland Metab. 2000;2(2):77-86. Persian.
5.
Daneshpour MS, Fallah MS, Sedaghati-Khayat B, Guity K, Khalili D, Hedayati M, et al. Rationale and design of a genetic study on cardiometabolic risk factors: Protocol for the Tehran Cardiometabolic Genetic Study (TCGS). JMIR Res Protoc. 2017;6(2). e28. [PubMed ID: 28232301]. [PubMed Central ID: PMC5344981]. https://doi.org/10.2196/resprot.6050.
6.
Faam B, Zarkesh M, Fallah MS, Hosseinzadeh N, Guity K, Hosseinpanah F. Heritability of obesity-related variables in Tehran families: Tehran lipid and glucose study. Scimetr. 2014;2(4). e18268. https://doi.org/10.5812/scimetr.18268.
7.
Zarkesh M, Daneshpour MS, Faam B, Fallah MS, Hosseinzadeh N, Guity K, et al. Heritability of the metabolic syndrome and its components in the Tehran lipid and glucose study (TLGS). Genet Res (Camb). 2012;94(6):331-7. [PubMed ID: 23374242]. https://doi.org/10.1017/S001667231200050X.
8.
Azizi F, Farahani ZK, Ghanbarian A, Sheikholeslami F, Mirmiran P, Momenan AA, et al. Familial aggregation of the metabolic syndrome: Tehran lipid and glucose study. Ann Nutr Metab. 2009;54(3):189-96. [PubMed ID: 19420912]. https://doi.org/10.1159/000217816.
9.
Al-Chalabi A, Almasy L. Genetics of complex human diseases: a laboratory manual. Cold Spring Harbor Laboratory Press; 2009.
10.
Azizi F, Ghanbarian A, Momenan AA, Hadaegh F, Mirmiran P, Hedayati M, et al. Prevention of non-communicable disease in a population in nutrition transition: Tehran lipid and glucose study Phase II. Trials. 2009;10:5. [PubMed ID: 19166627]. [PubMed Central ID: PMC2656492]. https://doi.org/10.1186/1745-6215-10-5.
11.
Halalkhor S, Mesbah-Namin SA, Daneshpour MS, Hedayati M, Azizi F. Association of ATP-binding cassette transporter-A1 polymorphism with apolipoprotein AI level in Tehranian population. J Genet. 2011;90(1):129-32. [PubMed ID: 21677398]. https://doi.org/10.1007/s12041-011-0030-9.
12.
Bandarian F, Daneshpour MS, Hedayati M, Naseri M, Azizi F. Identification of sequence variation in the apolipoprotein A2 gene and their relationship with serum high-density lipoprotein cholesterol levels. Iran Biomed J. 2016;20(2):84-90. [PubMed ID: 26590203]. [PubMed Central ID: PMC4726888].
13.
Bandarian F, Hedayati M, Daneshpour MS, Naseri M, Azizi F. Genetic polymorphisms in the APOA1 gene and their relationship with serum HDL cholesterol levels. Lipids. 2013;48(12):1207-16. [PubMed ID: 24081495]. https://doi.org/10.1007/s11745-013-3847-6.
14.
Daneshpour MS, Faam B, Hedayati M, Eshraghi P, Azizi F. ApoB (XbaI) polymorphism and lipid variation in Teharnian population. Eur J Lipid Sci Technol. 2011;113(4):436-40. https://doi.org/10.1002/ejlt.201000346.
15.
Daneshpour MS, Faam B, Mansournia MA, Hedayati M, Halalkhor S, Mesbah-Namin SA, et al. Haplotype analysis of Apo AI-CIII-AIV gene cluster and lipids level: Tehran lipid and glucose study. Endocrine. 2012;41(1):103-10. [PubMed ID: 22105741]. https://doi.org/10.1007/s12020-011-9526-6.
16.
Daneshpour MS, Zarkesh M, Hedayati M, Mesbah SMN, Halalkhor S, Faam B, et al. The G360t polymorphism in the APO AIV gene and its association with combined HDL/LDL cholesterol phenotype: Tehran lipid and glucose study. Int JEndocrinol Metab. 2010;2010(1):32-8.
17.
Daneshpour MS, Hedayati M, Eshraghi P, Azizi F. Association of Apo E gene polymorphism with HDL level in Tehranian population. Eur J Lipid Sci Technol. 2010;112(7):810-6. https://doi.org/10.1002/ejlt.200900207.
18.
Faam B, Daneshpour MS, Hedayati M, Halalkhor S, Mansournia MA, Zarkesh M, et al. The age effect on the association between the scavenger receptor class B type I (SR-BI) polymorphism and HDL-C level: Tehran lipid and glucose study. Endocr Res. 2014;39(3):91-3. [PubMed ID: 24738490]. https://doi.org/10.3109/07435800.2013.808207.
19.
Barkowski RS, Frishman WH. HDL metabolism and CETP inhibition. Cardiol Rev. 2008;16(3):154-62. [PubMed ID: 18414186]. https://doi.org/10.1097/CRD.0b013e31816a3b60.
20.
Daneshpour MS, Hedayati M, Azizi F. TaqI B1/B2 and -629A/C cholesteryl ester transfer protein (CETP) gene polymorphisms and their association with CETP activity and high-density lipoprotein cholesterol levels in a Tehranian population. Part of the Tehran lipid and glucose study (TLGS). Genet Mol Biol. 2007;30(4):1039-46. https://doi.org/10.1590/s1415-47572007000600001.
21.
Kashani Farid MA, Azizi F, Hedayati M, Daneshpour MS, Shamshiri AR, Siassi F. Association between CETP Taq1B and LIPC -514C/T polymorphisms with the serum lipid levels in a group of Tehran's population: A cross sectional study. Lipids Health Dis. 2010;9:96. [PubMed ID: 20822508]. [PubMed Central ID: PMC2944238]. https://doi.org/10.1186/1476-511X-9-96.
22.
Daneshpour M, Faam B, Hedayati M, Azizi F. [Presence of the X+ allele in apolipoprotein B gene increase the total cholesterol and apolipoprotein B concentration in Tehranian people]. Iran J Endocrinol Metab. 2011;12(6):588-93. Persian.
23.
Gretarsdottir S, Helgason H, Helgadottir A, Sigurdsson A, Thorleifsson G, Magnusdottir A, et al. A splice region variant in LDLR lowers non-high density lipoprotein cholesterol and protects against coronary artery disease. PLoS Genet. 2015;11(9). e1005379. [PubMed ID: 26327206]. [PubMed Central ID: PMC4556698]. https://doi.org/10.1371/journal.pgen.1005379.
24.
Boes E, Coassin S, Kollerits B, Heid IM, Kronenberg F. Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: A systematic in-depth review. Exp Gerontol. 2009;44(3):136-60. [PubMed ID: 19041386]. [PubMed Central ID: PMC2730542]. https://doi.org/10.1016/j.exger.2008.11.003.
25.
Naseri M, Hedayati M, Daneshpour MS, Bandarian F, Azizi F. Identification of genetic variants of lecithin cholesterol acyltransferase in individuals with high HDLC levels. Mol Med Rep. 2014;10(1):496-502. [PubMed ID: 24789697]. https://doi.org/10.3892/mmr.2014.2177.
26.
Naseri M, Hedayati M, Daneshpour MS, Bandarian F, Azizi F. A comparison of lecithin cholesterol acyltransferase gene variation among individuals with high and low HDL levels in Tehran lipid and glucose study (TLGS). Iran J Endocrinol Metab. 2015;17(3):206-14.
27.
National Cholesterol Education Program Expert Panel on Detection Evaluation; Treatment of High Blood Cholesterol in Adults. Third Report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (adult treatment panel III) final report. Circulation. 2002;106(25):3143-421. [PubMed ID: 12485966]. https://doi.org/10.1161/circ.106.25.3143.
28.
Alberti KG, Zimmet P, Shaw J. Metabolic syndrome--a new world-wide definition. A Consensus Statement from the International Diabetes Federation. Diabet Med. 2006;23(5):469-80. [PubMed ID: 16681555]. https://doi.org/10.1111/j.1464-5491.2006.01858.x.
29.
Alberti KG, Eckel RH, Grundy SM, Zimmet PZ, Cleeman JI, Donato KA, et al. Harmonizing the metabolic syndrome: A joint interim statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of Obesity. Circulation. 2009;120(16):1640-5. [PubMed ID: 19805654]. https://doi.org/10.1161/CIRCULATIONAHA.109.192644.
30.
Azizi F, Khalili D, Aghajani H, Esteghamati A, Hosseinpanah F, Delavari A, et al. Appropriate waist circumference cut-off points among Iranian adults: The first report of the Iranian National Committee of Obesity. Arch Iran Med. 2010;13(3):243-4. [PubMed ID: 20433230].
31.
Hosseini-Esfahani F, Daneshpour MS, Mirmiran P, Mehrabi Y, Hedayati M, Azizi F. Interaction of APOC3 polymorphism and dietary fats on the risk of metabolic syndrome. Iran J Endocrinol Metabo. 2015;16(5):345-55.
32.
Hosseini-Esfahani F, Mirmiran P, Daneshpour MS, Mottaghi A, Azizi F. The effect of interactions of single nucleotide polymorphisms of APOA1/APOC3 with food group intakes on the risk of metabolic syndrome. Avicenna J Med Biotechnol. 2017;9(2):94-103. [PubMed ID: 28496949]. [PubMed Central ID: PMC5410135].
33.
Fallah MS, Sedaghatikhayat B, Guity K, Akbari F, Azizi F, Daneshpour MS. The relation between metabolic syndrome risk factors and genetic variations of apolipoprotein v in relation with serum triglyceride and HDL-C level. Arch Iran Med. 2016;19(1):46-50. [PubMed ID: 26702748].
34.
Zadeh-Vakili A, Faam B, Daneshpour MS, Hedayati M, Azizi F. Association of CD36 gene variants and metabolic syndrome in Iranians. Genet Test Mol Biomarkers. 2012;16(4):234-8. [PubMed ID: 22047506]. [PubMed Central ID: PMC3326263]. https://doi.org/10.1089/gtmb.2011.0195.
35.
Javanrouh N, Daneshpour MS, Soltanian AR, Tapak L. Kernel machine SNP set analysis provides new insight into the association between obesity and polymorphisms located on the chromosomal 16q.12.2 region: Tehran lipid and glucose study. Gene. 2018;658:146-51. [PubMed ID: 29524577]. https://doi.org/10.1016/j.gene.2018.03.006.
36.
Sedaghati-Khayat B, Barzin M, Akbarzadeh M, Guity K, Fallah MS, Pourhassan H, et al. Lack of association between FTO gene variations and metabolic healthy obese (MHO) phenotype: Tehran Cardio-metabolic Genetic Study (TCGS). Eat Weight Disord. 2018. [PubMed ID: 29525920]. https://doi.org/10.1007/s40519-018-0493-2.
37.
Pilia G, Chen WM, Scuteri A, Orru M, Albai G, Dei M, et al. Heritability of cardiovascular and personality traits in 6,148 Sardinians. PLoS Genet. 2006;2(8). e132. [PubMed ID: 16934002]. [PubMed Central ID: PMC1557782]. https://doi.org/10.1371/journal.pgen.0020132.
38.
Eshraghi P, Hedayati M, Daneshpour MS, Mirmiran P, Azizi F. Association of body mass index and Trp64Arg polymorphism of the beta3-adrenoreceptor gene and leptin level in Tehran lipid and glucose study. Br J Biomed Sci. 2007;64(3):117-20. [PubMed ID: 17910280]. https://doi.org/10.1080/09674845.2007.11732769.
39.
Lalami ZA, Ebrahimi A, Daneshpour MS. [Evaluating the relation of rs1801282 polymorphism in PPAR-γ gene with obesity in Tehran lipid and glucose study (TLGS) participants]. Tehran Univ Med J. 2016;74(6):415-24. Persian.
40.
Hedayati M, Sharifi K, Rostami F, Daneshpour MS, Zarif Yeganeh M, Azizi F. Association between TNF-alpha promoter G-308A and G-238A polymorphisms and obesity. Mol Biol Rep. 2012;39(2):825-9. [PubMed ID: 21559831]. [PubMed Central ID: PMC3249554]. https://doi.org/10.1007/s11033-011-0804-4.
41.
Georgia S, Bhushan A. Beta cell replication is the primary mechanism for maintaining postnatal beta cell mass. J Clin Invest. 2004;114(7):963-8. [PubMed ID: 15467835]. [PubMed Central ID: PMC518666]. https://doi.org/10.1172/JCI22098.
42.
Steinthorsdottir V, Thorleifsson G, Sulem P, Helgason H, Grarup N, Sigurdsson A, et al. Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes. Nat Genet. 2014;46(3):294-8. [PubMed ID: 24464100]. https://doi.org/10.1038/ng.2882.
43.
American Diabetes A. Standards of medical care in diabetes--2013. Diabetes Care. 2013;36 Suppl 1:S11-66. [PubMed ID: 23264422]. [PubMed Central ID: PMC3537269]. https://doi.org/10.2337/dc13-S011.
44.
Taurog A, Dorris M, Doerge DR. Evidence for a radical mechanism in peroxidase-catalyzed coupling. I. Steady-state experiments with various peroxidases. Arch Biochem Biophys. 1994;315(1):82-9. [PubMed ID: 7979410]. https://doi.org/10.1006/abbi.1994.1474.
45.
Jaume JC, Burek CL, Hoffman WH, Rose NR, McLachlan SM, Rapoport B. Thyroid peroxidase autoantibody epitopic 'fingerprints' in juvenile Hashimoto's thyroiditis: Evidence for conservation over time and in families. Clin Exp Immunol. 1996;104(1):115-23. [PubMed ID: 8603516]. [PubMed Central ID: PMC2200393]. https://doi.org/10.1046/j.1365-2249.1996.d01-659.x.
46.
Bakker B, Bikker H, Vulsma T, de Randamie JS, Wiedijk BM, De Vijlder JJ. Two decades of screening for congenital hypothyroidism in The Netherlands: TPO gene mutations in total iodide organification defects (an update). J Clin Endocrinol Metab. 2000;85(10):3708-12. [PubMed ID: 11061528]. https://doi.org/10.1210/jcem.85.10.6878.
47.
Fugazzola L, Mannavola D, Vigone MC, Cirello V, Weber G, Beck-Peccoz P, et al. Total iodide organification defect: Clinical and molecular characterization of an Italian family. Thyroid. 2005;15(9):1085-8. [PubMed ID: 16187919]. https://doi.org/10.1089/thy.2005.15.1085.
48.
Hedayati M, Salehi Jahromi M, Zarif Yeganeh M, Daneshpour MS, Hoghooghi Rad L, Azizi F. Association between serum level of anti-TPO titer and polymorphisms G1193/C Exon 8 and C2145/T Exon 12 of thyroid peroxidase gene in an Iranian population. Int J Endocrinol Metab. 2010;8(2):64-7.
49.
Faam B, Daneshpour MS, Azizi F, Hedayati M. Association of T2229/C Exon 12 polymorphisms of thyroid peroxidase gene with anti-TPO levels in Tehran population. J Zanjan Univ Med Sci. 2011;19(74):37-43.
50.
Asuncion M, Calvo RM, San Millan JL, Sancho J, Avila S, Escobar-Morreale HF. A prospective study of the prevalence of the polycystic ovary syndrome in unselected Caucasian women from Spain. J Clin Endocrinol Metab. 2000;85(7):2434-8. [PubMed ID: 10902790]. https://doi.org/10.1210/jcem.85.7.6682.
51.
Mehrabian F, Khani B, Kelishadi R, Ghanbari E. The prevalence of polycystic ovary syndrome in Iranian women based on different diagnostic criteria. Endokrynol Pol. 2011;62(3):238-42. [PubMed ID: 21717406].
52.
Ramezani Tehrani F, Daneshpour M, Hashemi S, Zarkesh M, Azizi F. Relationship between polymorphism of insulin receptor gene, and adiponectin gene with PCOS. Iran J Reprod Med. 2013;11(3):185-94. [PubMed ID: 24639745]. [PubMed Central ID: PMC3943219].
53.
Hahn S, Haselhorst U, Tan S, Quadbeck B, Schmidt M, Roesler S, et al. Low serum 25-hydroxyvitamin D concentrations are associated with insulin resistance and obesity in women with polycystic ovary syndrome. Exp Clin Endocrinol Diabetes. 2006;114(10):577-83. [PubMed ID: 17177140]. https://doi.org/10.1055/s-2006-948308.
54.
Wehr E, Pilz S, Schweighofer N, Giuliani A, Kopera D, Pieber TR, et al. Association of hypovitaminosis D with metabolic disturbances in polycystic ovary syndrome. Eur J Endocrinol. 2009;161(4):575-82. [PubMed ID: 19628650]. https://doi.org/10.1530/EJE-09-0432.
55.
Yildizhan R, Kurdoglu M, Adali E, Kolusari A, Yildizhan B, Sahin HG, et al. Serum 25-hydroxyvitamin D concentrations in obese and non-obese women with polycystic ovary syndrome. Arch Gynecol Obstet. 2009;280(4):559-63. [PubMed ID: 19214546]. https://doi.org/10.1007/s00404-009-0958-7.
56.
Styrkarsdottir U, Helgason H, Sigurdsson A, Norddahl GL, Agustsdottir AB, Reynard LN, et al. Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis. Nat Genet. 2017;49(5):801-5. [PubMed ID: 28319091]. https://doi.org/10.1038/ng.3816.
57.
Hosseini-Esfahani F, Mirmiran P, Daneshpour MS, Mehrabi Y, Hedayati M, Soheilian-Khorzoghi M, et al. Dietary patterns interact with APOA1/APOC3 polymorphisms to alter the risk of the metabolic syndrome: The Tehran lipid and glucose study. Br J Nutr. 2015;113(4):644-53. [PubMed ID: 25653052]. https://doi.org/10.1017/S0007114514003687.
58.
Zarkesh M, Daneshpour MS, Hedayati M, Azizi F. [Association of apolipoprotein A-IV gene G360T polymorphism with metabolic syndrome: Tehran lipid and glucose study]. Iran J Endocrinol Metab. 2012;14(1):10-7. Persian.
59.
Zarkesh M, Daneshpour MS, Faam B, Hedayati M, Azizi F. Is there any association of apolipoprotein E gene polymorphism with obesity status and lipid profiles? Tehran lipid and glucose study (TLGS). Gene. 2012;509(2):282-5. [PubMed ID: 22921891]. https://doi.org/10.1016/j.gene.2012.07.048.
60.
Zadeh Vakili A, Faam B, Daneshpour MS, Hedayati M, Azizi F. [Association of rs10499859 A> G and rs13246513 C> T variants of CD36 gene and metabolic syndrome: TLGS]. Iran J Endocrinol Metab. 2013;15(1):86-93. Persian.
61.
Moslehizadeh V, Ajamian F, Ebrahimi A, Delshad Siahkali H. [Association of FABP2 gene polymorphism (rs1799883) with risk of obesity in the Tehran lipid and glucose study (TLGS) population]. Tehran Univ Med J. 2016;73(12):864-71. Persian.
62.
Hosseini-Esfahani F, Koochakpoor G, Daneshpour MS, Sedaghati-Khayat B, Mirmiran P, Azizi F. Mediterranean dietary pattern adherence modify the association between FTO genetic variations and obesity phenotypes. Nutrients. 2017;9(10). [PubMed ID: 28954439]. [PubMed Central ID: PMC5691681]. https://doi.org/10.3390/nu9101064.
63.
Rostami F, Hosseini H, Sharifi K, Daneshpour M, Azizi F, Hedayati M. Association of G-174C polymorphism of the interleukin-6 gene promoter with obesity in Iranian population. World Acad Sci Eng Technol. 2010;4(9):400-3.
64.
Naseri M, Hedayati M, Daneshpour MS, Bandarian F, Azizi F. Association of lecithin cholesterol acyltransferase rs5923 polymorphism in Iranian individuals with extremely low high-density lipoprotein cholesterol: Tehran lipid and glucose study. Iran Biomed J. 2015;19(3):172-6. [PubMed ID: 26117245]. [PubMed Central ID: PMC4571013].
65.
Daneshpour MS, Hedayati M, Azizi F. Hepatic lipase C-514T polymorphism and its association with high-density lipoprotein cholesterol level in Tehran. Eur J Cardiovasc Prev Rehabil. 2006;13(1):101-3. [PubMed ID: 16449872]. https://doi.org/10.1097/01.hjr.0000183908.74989.0c.
66.
Koochakpoor G, Daneshpour MS, Mirmiran P, Hosseini SA, Hosseini-Esfahani F, Sedaghatikhayat B, et al. The effect of interaction between Melanocortin-4 receptor polymorphism and dietary factors on the risk of metabolic syndrome. Nutr Metab (Lond). 2016;13:35. [PubMed ID: 27186233]. [PubMed Central ID: PMC4867980]. https://doi.org/10.1186/s12986-016-0092-z.
67.
Koochakpoor G, Hosseini-Esfahani F, Daneshpour MS, Hosseini SA, Mirmiran P. Effect of interactions of polymorphisms in the Melanocortin-4 receptor gene with dietary factors on the risk of obesity and type 2 diabetes: A systematic review. Diabet Med. 2016;33(8):1026-34. [PubMed ID: 26666384]. https://doi.org/10.1111/dme.13052.

comments