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Evidence-Based Complementary and Alternative Medicine
Volume 2011 (2011), Article ID 106390, 7 pages
Original Article

Genetic Effects of FTO and MC4R Polymorphisms on Body Mass in Constitutional Types

Division of Constitutional Medicine Research, Korea Institute of Oriental Medicine, 483 Exporo, Yuseong-gu, Daejeon, 305-811, Republic of Korea
Department of Genetic Epidemiology, SNP Genetics Inc., Geumcheon-gu, Seoul, Republic of Korea
Kirin Oriental Medical Hospital, Seoul, Republic of Korea
Department of Life Science, Sogang University, Mapo-gu, Seoul, Republic of Korea

Received 2 March 2009; Accepted 13 September 2009

Copyright © 2011 Seongwon Cha et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Sasang constitutional medicine (SCM), a Korean tailored medicine, categorizes human beings into four types through states of physiological imbalances and responsiveness to herbal medicine. One SCM type susceptible to obesity seems sensitive to energy intake due to an imbalance toward preserving energy. Common variants of fat mass and obesity associated (FTO) and melanocortin 4 receptor (MC4R) genes have been associated with increased body mass index (BMI) by affecting energy intake. Here, we statistically examined the association of FTO and MC4R polymorphisms with BMI in two populations with 1370 Koreans before and after SCM typing, and with the lowering of BMI in 538 individuals who underwent a 1-month lifestyle intervention. The increased BMI replicated the association with FTO haplotypes (effect size 1.1 kg/m2) and MC4R variants (effect size 0.64 kg/m2). After the lifestyle intervention, the carriers of the haplotype represented by the minor allele of rs1075440 had a tendency to lose more waist-to-hip ratio (0.76%) than non-carriers. The constitutional discrepancy for the accumulation of body mass by the effects of FTO and/or MC4R variants seemed to reflect the physique differences shown in each group of SCM constitutional types. In conclusion, FTO and MC4R polymorphisms appear to play an important role in weight gain, while only FTO variants play a role in weight loss after lifestyle intervention. Different trends were observed among individuals of SCM types, especially for weight gain. Therefore, classification of individuals based on physiological imbalance would offer a good genetic stratification system in assessing the effects of obesity genes.

1. Introduction

Common variations in the first intron of the fat mass and obesity associated (FTO) gene, have been shown to be risk factors for obesity in several studies of Caucasian [13], Asian [49] and African American [10] subjects. However, conflicting results have been generated in certain Asian (e.g., Japanese and Chinese) [11, 12] and African American [3] populations. These inconsistencies may stem from certain genetic or non-genetic factors that were not taken into account by the study authors [13].

For these reasons, we became interested in a traditional Korean medicine approach that uses constitutional typing and novel stratification criteria to assess the risk factors for obesity in humans with different genetic compositions. Sasang constitutional medicine (SCM), a branch of traditional Korean medicine, is a unique personalized medical system that classifies humans into four constitutional types based primarily on their responses to herbal medicine, along with an individual's physiological, psychological and physical characteristics. Recently, there have been efforts to explain the constitution concept of SCM with the language of modern genetics [14], and to search for a genetic linkage to SCM on a genome-wide scale [15]. The underlying principle of this classification stems from the concept that each individual is born in one of four physiologically unbalanced states: the Taeyang (TY), Tae-eum (TE), Soyang (SY) or Soeum (SE) [16, 17]. The TE type is dominant in preservative function (mainly by liver and small intestine) over respiratory function (mainly by lung), whereas the TY type has an opposite dominance. This interrelation is also maintained between the SY and SE types, that is, the SY type has strong digestive function (mainly by stomach and pancreas) over excretive function (mainly by kidney and large intestine), whereas the SE type has a countertrend. Therefore, the TE type is thought to display a strong physiological tendency to become obese by preserving energy; TE types tend to gain more weight and achieve a larger waist circumference than other types [17]. Bioelectrical impedance analyses have shown that the TE type is associated with a high body fat mass [18]. Thus, it may be possible to achieve more delicate and stringent analyses of the risk factors for obesity via the stratification of populations according to SCM typing.

The FTO gene has been associated with food intake [1921] and reduced satiety response [22], and the genetic effect on obesity is attenuated by physical activity [23]. However, this gene does not appear to influence changes in body weight or fat distribution in people who have undergone 1 or 2 years of intervention (e.g., exercise and dietary control) [24, 25]. We are also interested in the melanocortin 4 receptor (MC4R) gene. MC4R is similar to FTO in terms of its role in the regulation of food intake, although it has an additional effect on energy expenditure [26]. Recent two genome-wide association studies revealed that common allelic variants in MC4R locus are associated with obesity-related phenotypes [27, 28]. In addition, the common variants near MC4R have been found to have additive effects on body mass index (BMI) along with FTO variants [28].

Here, we examine the genetic effects of FTO and MC4R variants on obesity-related phenotypes. We assessed the relationship between lifestyle intervention and common variants of the genes with obesity-related phenotypes in individuals of each SCM type.

2. Methods

2.1. Subjects

We recruited 835 individuals from an obesity clinic in Kirin Oriental Medical Hospital (Seoul, Korea) (this population is hereafter named Kirin) between 2001 and 2004, and 535 individuals were recruited from 12 other oriental medical hospitals in Korea (this population is hereafter named Multicenter) during a 2-year period starting from 2007. The enrolled subjects did not include patients with chronic diseases, such as hypertension, coronary artery disease, stroke, diabetes, hyperlipidemia, and so forth. Written informed consent was obtained from all subjects and the Institutional Review Board of the Korea Institute of Oriental Medicine approved the study protocol. Abdominal fat area was measured using computerized tomography (CT) cross-sectional images, as previously described [29] (Hispeed CT/e, GE, USA). Blood samples were obtained for biochemical measurements, and DNA was extracted from each subject and stored at −70°C until further use. The characteristics of the recruited individuals are shown in Table 1. There were more women than men in our study population (Table 1), possibly because women tend to attend obesity clinic more frequently than men do. Therefore, we considered sex as a covariate in our linear regression analyses to minimize the effects of this bias.

Table 1: Anthropometric and clinical characteristics of the subjectsa.
2.2. Subgrouping by Sasang Constitution

The classification of Sasang constitution is performed based on three main factors: physique and facial appearance, psychological character, and physiological and pathological reactions. As for the appearance, individuals with TE type tend to have bigger physiques than those with SY and SE types [18], and the subjects of SY type usually have smaller hip than those of SE type. Individuals with SE and SY types have psychological characters reciprocal to each other. The SY type subjects, more than the SE types, have been found to be more extroverted in their performance on Myers-Briggs Type Indicator [18] and to show higher score for Novelty Seeking and lower score for Harm Avoidance from Temperament and Character Inventory [30]. Because each type has been known to have type-specific physiological imbalances as described in the introduction [16, 17], important pathological symptoms are different among the Sasang types: bowel movements and constipation for the SY type, perspiration for the TE type and digestion for the SE type.

The constitutional types of the 835 subjects recruited from the obesity clinic were categorized by an oriental medical doctor with the self-reported Questionnaire for the Sasang Constitution Classification (QSCC) [18] using Win QSCC II software, version 99 (Ssord Medicom & Ssord OMS, Seoul, Korea). QSCC including the questionnaires on the three main factors for constitution classification was developed in 1993 and upgraded to the present version (QSCC II) in 1996 [31]. In the latter version, 1366 individuals (48.9% males; age 10–60 years) whose constitutions had been determined by professional clinicians were used for standardization and 265 subjects were assessed for validation. The internal consistency of each constitution was measured by Cronbach's α: 0.57 for TY type, 0.59 for TE type, 0.57 for SY type and 0.63 for SE type. The diagnostic discriminability of QSCC II was 70% overall in hit-ratio (75% for TE type, 60% for SY type, 71% for SE type). Professional SCM doctors, taking into account the typing from the questionnaire, categorized the constitutional types of the 535 subjects according to responsiveness to herbal medicine and diagnosis. The constitutional types of 24 subjects in the Multicenter population were not characterized.

2.3. Weight-Control Program

After removing subjects who had not fulfilled a 1-month weight-control program, a subgroup of subjects ( ) from the Kirin population was selected to be analyzed for the genetic effects of FTO and MC4R variants on weight loss after the 1-month lifestyle intervention. The intervention program consisted of a low-calorie diet (~600 kcal per day: breakfast with uncooked food 85 kcal and soybean milk 120 kcal, lunch 200 kcal, Chegamuiyiin-tang 186.3 kcal), daily exercise using a treadmill machine (5 km/h for 45 min to 1 hr), an electrolipolysis treatment using Lipodren equipment (Sormedic, Barcelona, Spain) and the administration of Chegamuiyiin-tang (three times per day) containing 17 herbs. The prescription of Chegamuiyiin-tang for 1 day was as follows: Cocicis Semen 66 g, Rehmanniae Radix Preparata 33 g, Angelicae Gigantis Radix 16 g, Raphani Semen 12 g, Akebiae Lignum 12 g, Plantaginis Semen 12 g, Astragali Radix 12 g, Gastrodiae Rhizoma 12 g, Mori Cotex Radicis 12 g, Glycyrrhizae Radix 12 g, Thujae Semen 12 g, Lycii Fructus 8 g, Cnidii Rhizoma 4 g, Carthami Flos 4 g, Caesalpiniae Lignum 4 g, Cervi Parvum Cornu 4 g and Cervi Cornu 12 g. The subjects were asked to keep a daily diet diary to help maintain the low-calorie diet. Changes in anthropometric features were measured by a bio-impedance analysis using a commercial device (Inbody 2.0 Biospace, Seoul, Korea).

2.4. Genotyping of Single Nucleotide Polymorphism

Genotyping was performed using the TaqMan system [32] with amplifying primers and TaqMan probes (Applied Biosystems, Foster City, CA, USA). Two FAM and VIC dyes were labeled on each allelic probe. PCR was performed in 384-well plates. Genomic templates were amplified in a total reaction volume of 5 μl, containing TaqMan Universal Master Mix (Applied Biosystems), 900 nmol/l of PCR primer, 200 mmol/l of TaqMan probe and 20 ng of genomic DNA. Amplification was performed via a heating cycle (50°C for 2 min and 95°C for 10 min), followed by an amplifying cycle (40 cycles of 95°C for 15 s, 60°C for 1 min) in a thermal cycler (PE 9700, Applied Biosystems). Fluorescence intensity was measured using a Prism 7900HT (Applied Biosystems).

2.5. Statistics

We used the -test to determine if the variants of FTO and MC4R were in Hardy-Weinberg equilibrium. Analysis of variance was used to check if the characteristics in Table 1 differed according to SCM types. Linkage disequilibrium (LD; Lewontin's ) and haplotype structures were obtained from the Haploview program, version 4.1 (Daly Lab at the Broad Institute, Cambridge, MA, USA) [33]. Haplotypes of the FTO single nucleotide polymorphism (SNPs) were constructed using Phase (version 2.1), a Bayesian algorithm-based program [34, 35]. The relationships of FTO and MC4R with obesity-related traits were analyzed via linear regression analyses, with adjustments for age and gender as covariates. Meta-analysis was performed in a mixed model using SAS, according to the instruction previously reported [36]. We use Storey's q-value method of measuring for the minimum false discovery rate to control the significant level -value for each hypothesis test related to haplotype or SNP in multiple comparisons [37]. Effect sizes were presented as changes in the minor allele carriage, determined via a linear regression analysis. All statistical analyses were performed using SAS, version 8.02 (SAS, Cary, NC, USA) and Matlab, version 7.6 (MathWorks, Natick, MA, USA).

3. Results

3.1. Characteristics of Common Variants

Using international Japanese and Chinese HapMap databases, we searched 23 validated SNPs that were previously reported to reside in the first intron of FTO [1, 2] (Supplementary Table 1). The Chinese and Japanese HapMap databases provide a robust platform for studies in a Korean population. We then constructed the LD structure using 14 SNPs (Figure 1(a)) that did not demonstrate complete LD with other SNPs and did not have minor allele frequencies <10%. This resulted in three LD blocks. Each block consisted of three haplotypes, which were selected using a cutoff of 10% haplotype frequencies (Figures 1(b) and 1(c)). Haplotypes were named with the abbreviated LD block name, followed by the haplotypes (in order of frequency) in each block (e.g., bl3-ht1 indicates the most frequent haplotype in LD block 3). In the cases of bl1-ht1 and bl2-ht1 with over 50% haplotype frequencies (Figure 1(b)), we used the other minor haplotypes in each block as interesting risk haplotypes in order to avoid confusion in interpreting the association results and designated them bl1-ht1r and bl2-ht1r (“r” indicates risk). We selected two common variants (rs17782313 and rs12970134) near MC4R that had previously been reported in two independent genome-wide association studies [27, 28]. Two haplotypes of FTO, bl2-ht3 and bl3-ht3, were more frequent (3-4%) in the Kirin population than in the Multicenter population, as the individuals in Kirin were heavier. Similarly, two SNPs near MC4R were more frequent (3-4%) in the Kirin population. The FTO and MC4R alleles were determined to be in Hardy-Weinberg equilibrium in each population ( ).

Figure 1: The LD (a) and haplotype (b) structures of FTO were determined via Haploview program. In FTO haplotypes, blue and red colors indicate major and minor alleles of each SNP, while thick and thin lines between blocks indicate >10% and >1% connecting frequencies, respectively, between haplotypes in neighboring blocks (b). (c) Among the 14 SNPs previously reported to reside in the first intron of FTO, three, two and eight SNPs are located in block 1 (bl1), block 2 (bl2) and block 3 (bl3), respectively.
3.2. Increased Effects of FTO and MC4R in the TE Type

Association analyses were performed on the three haplotypes in each LD block of FTO and two SNPs of MC4R in two Korean populations. We observed that haplotype frequencies of FTO were correlated with SCM type in a Multicenter population, but that minor allele frequencies of MC4R SNPs were not related with SCM type in the Multicenter population. The effect size (i.e. the unit change caused by the carriage of risk allele) was calculated via linear regression analysis under an additive model as done in previous reports.

For the Kirin population, two FTO haplotypes (bl2-ht3 and bl3-ht3) were associated with increased BMI in all subjects and the subjects of TE types (Supplementary Table 2). Both bl2-ht3 and bl3-ht3 showed stronger effect sizes in TE types (for both bl2-ht3 and bl3-ht3, there was a 1.4-fold increase in effect size) than in all subjects (Figure 2(a)). The minor alleles of three FTO SNPs tagging the above haplotypes (rs7206790 in bl2-ht3, rs17817449 and rs1121980 in bl3-ht3) were also associated with increased BMI in TE types (Supplementary Table 3). Two MC4R SNPs were also associated with increased BMI (Supplementary Table 2) in all subjects and the subjects of TE types, as previously reported [27, 28]. There were no genetic effects of FTO and MC4R in SY and SE types. For the Multicenter population, the statistical analyses performed using a dominant model because the number of minor allele homozygotes of three SNPs (rs7206790, rs1121980 and rs17817449) was very small. We did not find any associations of FTO or MC4R in the Multicenter population (Supplementary Table 4).

Figure 2: A hypothetical diagram on the relationships between the variants of FTO and/or MC4R and weight changes in the context of TE constitutional type (a). The interaction of the obesity-related variants and TE type may be strong for weight gain especially in a heavy population (Kirin population in this study). Strong correlation was found between the effects of FTO haplotypes and MC4R SNPs on body mass (BMI and WHR) and clinically measured body mass (BMI and WHR) in each SCM type (b). The action of the genes in the context of SCM type may differently affect body mass changes in each type. The size of inequality sign indicates the size of body mass difference between SCM types.

In combining the two populations, we can find the strong association of FTO haplotypes (bl2-ht1r, bl2-ht3 and bl3-ht3) and MC4R SNPs (rs17782313 and rs12970134) with increased BMI in all subjects (Supplementary Table 5). In SCM types, two FTO haplotypes (bl2-ht3 and bl3-ht3) had an effect on BMI increase only in subjects of TE type. When we searched the combinatorial effects of FTO and MC4R variants, we found that the association signal of FTO haplotypes on BMI became stronger (for bl2-ht3, 2.0-fold increase of effect size in Kirin population and 1.5-fold increase in combined population; for bl3-ht3, 2.1-fold increase of effect size in Kirin population and 1.7-fold increase in combined population) in the minor allele carriers of MC4R rs17782313 (Supplementary Table 6).

3.3. Weight Loss in Response to Lifestyle Intervention

A subgroup of subjects ( ) recruited from a Kirin population participated in a 1-month weight-control program to assess the relationship between the obesity-related genes and body fat mass in response to lifestyle intervention. The percentage of body mass change is shown in Table 1. One percent indicates one-hundredth of the value of body mass change after the weight-control program divided by the value before the program. Obesity-related phenotypes including BMI and waist-to-hip ratio (WHR) were reduced after participation in the weight-control program. On average, the BMI and WHR decreased by 7.9% and 3.1%, respectively. Interestingly, the subjects of SY types showed only a small decrease of BMI (5.7%) and WHR (1.9%), compared with those of other types ( for BMI loss and for WHR loss).

Statistical analyses were performed using a dominant model because the number of minor allele homozygotes was very small after stratifying by SCM type. We found an association of an FTO haplotype (bl1-ht1r) with WHR loss in all subjects (Supplementary Table 7), but not with BMI loss in all subjects (Supplementary Table 8). When we stratified the subjects according to SCM type, the FTO haplotypes appeared to be related with BMI loss only in SY type subjects (Supplementary Table 8). However, we cannot conclude that there is an association between FTO haplotypes and BMI loss in the subjects of SY type, because the number of SY type subjects is very small. A replication analysis with another population is necessary to confirm the relationship between the haplotype and BMI loss in the subjects of SY type. We did not find any relationships between MC4R and the percentage of body mass change.

4. Discussion

Consistent with previous studies, we replicated the association of MC4R with BMI in a Korean population for the first time and we also confirmed the association of the FTO LD block with obesity-related phenotypes in Koreans. Our findings revealed that the haplotypes represented by minor alleles of three SNPs (rs17817449, rs1121980 and rs7206790) located within the first intron of FTO were associated with body mass (Supplementary Tables 2 and 5). The association of two SNPs near MC4R with BMI was well replicated in the Kirin population (26.5 kg/m2), therefore the association of MC4R variants with BMI could be found in the heavy population. To our knowledge, this replication with the common variants near MC4R is the first report in an East Asian population, although there have been several replicated results in Caucasians [27, 28]. As previously reported [28], the variants of FTO and MC4R had an additive effect on BMI increase, because the risk allele carriers of both FTO and MC4R variants showed approximately 2.0-fold strengthened susceptibility to body mass accumulation.

We expected that the effects of FTO and MC4R on body fat mass would be more apparent if the population were stratified by SCM type, as a previous report [18] has demonstrated distinct susceptibilities to obesity among subjects with different SCM types. Our recruited populations consisted of a large proportion of subjects with the TE type (Table 1). This was not surprising, considering that the TE type belongs to almost half of the Koreans and is prevalent in overweight populations [18, 38]. However, it would have been optimal to recruit additional subjects of the SY and SE types to boost the statistical power of our analysis.

When the population was stratified by SCM type (excluding subjects with the rare TY type; 0.6% of our study population), we observed different relationships of FTO and MC4R with obesity-related phenotypes (Supplementary Tables 2 and 5). In meta-analyses, MC4R SNPs had no significant effect on BMI increase in the subjects of TE type; therefore MC4R variants might show a strong association with BMI in the heavier Kirin population (mean BMI of TE type: 27.2 kg/m2) than in the Multicenter population (mean BMI of TE type: 25.0 kg/m2) (Figure 2(a)). The relationship between obesity and the TE type by the risk alleles of FTO and MC4R was consistent with the findings of a previous report, which indicated that TE subjects tend to have higher fat masses [18]. In the subjects of SE and SY types, we observed no relationship between variants and body mass. Therefore, specific alleles may confer different susceptibilities to increased body mass in subjects with TE type or not; the genetic differences appear to be similar to the clinical differences in BMI between TE type and the other types (Table 1 and Figure 2).

The genetic factors in the same haplotype may exert different effects on FTO expression in TE type subjects over other type subjects, in response to energy-preserving action including increased nutritional intake, decreased physical activity and so on. The interaction of the haplotypes and SCM types might be important for weight gain (Figure 2(a)). Therefore, the values of body mass in the subjects of SCM TE type and other types (Table 1) also corresponded with the effects of FTO haplotypes in the subjects of TE type and others (Figure 2(b)).

We revealed that individuals harboring the high-risk allele of FTO (also with MC4R) had no more significant propensity for BMI loss than other individuals. This corresponded with the information from previous studies that FTO does not appear to influence changes in body mass with the lifestyle intervention using exercise and dietary control [24, 25]. However, WHR loss was significantly associated with FTO haplotype (bl1-ht1r) in all subjects (Supplementary Table 7). Two previous reports on lifestyle interventions have shown an association with rs8050136 and rs9939609. Both SNPs are in complete LD with rs17817449 in a white population [1] and rs9939609 is in complete LD with rs17817449 in the population evaluated here. We similarly did not find any effect of loss in body mass with rs17817449 (Supplementary Table 9). Therefore, it would be necessary to search the effect on weight loss with another FTO variant (e.g., rs1075440 constructing bl1-ht1r haplotype).

The FTO is abundantly expressed in the hypothalamic nucleus, where it helps regulate energy homeostasis [2, 39]. A previous study in mice revealed that FTO mRNA expression (FTO encodes a 2-oxoglutarate-dependent nucleic acid demethylase) is regulated by nutritional intake and that it oscillates in response to feeding and fasting [39]. After a 1-month weight control containing low-calorie diet, the carriers of the obesity-risk alleles might undergo significant changes in FTO mRNA expression within the hypothalamic nuclei. Thus, future studies should examine the genetic factors that regulate FTO expression and attempt to link the methylation status of FTO to changes in body mass.

Consistent with previous reports [2, 27], accumulation in WHR by the action of FTO and MC4R variants was observed in all subjects and TE type subjects (Supplementary Table 10). Increased abdominal fat mass was associated with the variants of FTO and MC4R only in TE type subjects (Supplementary Table 11). This phenomenon is consistent with the tendency of TE type subjects to have thicker waistlines [17]. Therefore, we can see constitutional difference in the case of waist mass accumulation between TE type and the other types (Figure 2).

In conclusion, our findings demonstrate that the association of FTO and/or MC4R with increased weight gain in all subjects was primarily maintained in the subjects of TE type, who are considered to have a tendency to preserve energy rather than to expend it [17]. The genetic background of subjects differs according to SCM type (especially TE type), much like genetic background differs in subjects of different ethnicities and sex. Ethnic differences may be caused by the compositions of each SCM type in the populations, thereby accounting for the controversial results observed in several previous Asian studies. Specifically, when certain ethnic populations have fewer members with TE type and more members with SY and SE types, the relationship between the FTO gene and obesity may become weak. It would therefore be helpful to stratify the people according to physiological constitution types, as seen in SCM, to precisely assess the genetic effects on obesity-related phenotypes.

Supplementary Data

Supplementary data are available at eCAM online.


Korea Science and Engineering Foundation (KOSEF) grant funded by the Korean government (MEST) (Grant No. M10643020004-08N4302-00400).


The authors thank Myounggeun Kim for his assistance with data interpretation. I. Koo and B. L. Park contributed equally to this work.


  1. C. Dina, D. Meyre, S. Gallina et al., “Variation in FTO contributes to childhood obesity and severe adult obesity,” Nature Genetics, vol. 39, no. 6, pp. 724–726, 2007. View at Publisher · View at Google Scholar · View at PubMed
  2. T. M. Frayling, N. J. Timpson, M. N. Weedon et al., “A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity,” Science, vol. 316, no. 5826, pp. 889–894, 2007. View at Publisher · View at Google Scholar · View at PubMed
  3. A. Scuteri, S. Sanna, W.-M. Chen et al., “Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits,” PLoS Genetics, vol. 3, article e115, 2007. View at Publisher · View at Google Scholar · View at PubMed
  4. S. W. Cha, S. M. Choi, K. S. Kim et al., “Replication of genetic effects of FTO polymorphisms on BMI in a Korean population,” Obesity, vol. 16, no. 9, pp. 2187–2189, 2008. View at Publisher · View at Google Scholar · View at PubMed
  5. K. Hotta, Y. Nakata, T. Matsuo et al., “Variations in the FTO gene are associated with severe obesity in the Japanese,” Journal of Human Genetics, vol. 53, no. 6, pp. 546–553, 2008. View at Publisher · View at Google Scholar · View at PubMed
  6. A. F. Marvelle, L. A. Lange, L. Qin, L. S. Adair, and K. L. Mohlke, “Association of FTO with Obesity-Related traits in the cebu longitudinal health and nutrition survey (CLHNS) cohort,” Diabetes, vol. 57, no. 7, pp. 1987–1991, 2008. View at Publisher · View at Google Scholar · View at PubMed
  7. M. C. Y. Ng, K. S. Park, B. Oh et al., “Implication of genetic variants near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in type 2 diabetes and obesity in 6,719 Asians,” Diabetes, vol. 57, no. 8, pp. 2226–2233, 2008. View at Publisher · View at Google Scholar · View at PubMed
  8. Y.-C. Chang, P.-H. Liu, W.-J. Lee et al., “Common variation in the fat mass and Obesity-Associated (FTO) gene confers risk of obesity and modulates BMI in the chinese population,” Diabetes, vol. 57, no. 8, pp. 2245–2252, 2008. View at Publisher · View at Google Scholar · View at PubMed
  9. J. T. Tan, R. Dorajoo, M. Seielstad et al., “FTO variants are associated with obesity in the chinese and malay populations in Singapore,” Diabetes, vol. 57, no. 10, pp. 2851–2857, 2008. View at Publisher · View at Google Scholar · View at PubMed
  10. S. F. A. Grant, M. Li, J. P. Bradfield et al., “Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP,” PLoS ONE, vol. 3, no. 3, Article ID e1746, 2008. View at Publisher · View at Google Scholar · View at PubMed
  11. M. Horikoshi, K. Hara, C. Ito et al., “Variations in the HHEX gene are associated with increased risk of type 2 diabetes in the Japanese population,” Diabetologia, vol. 50, no. 12, pp. 2461–2466, 2007. View at Publisher · View at Google Scholar · View at PubMed
  12. H. Li, Y. Wu, R. J. F. Loos et al., “Variants in the fat mass- and obesity-associated (FTO) gene are not associated with obesity in a Chinese Han population,” Diabetes, vol. 57, no. 1, pp. 264–268, 2008. View at Publisher · View at Google Scholar · View at PubMed
  13. L. R. Cardon and J. I. Bell, “Association study designs for complex diseases,” Nature Reviews Genetics, vol. 2, no. 2, pp. 91–99, 2001. View at Publisher · View at Google Scholar · View at PubMed
  14. B.-Y. Kim, S. Cha, H.-J. Jin, and S. Jeong, “Genetic approach to elucidation of sasang constitutional medicine,” Evidence-Based Complementary and Alternative Medicine, vol. 6, supplement 1, pp. 51–57, 2009. View at Publisher · View at Google Scholar · View at PubMed
  15. H.-H. Won, S. Lee, E. Jang et al., “A genome-wide scan for the sasang constitution in a korean family suggests significant linkage at chromosomes 8q11.22-23 and 11q22.1–3,” Journal of Alternative and Complementary Medicine, vol. 15, no. 7, pp. 765–769, 2009. View at Publisher · View at Google Scholar · View at PubMed
  16. J. Lee, Longevity & Life Preservation In Oriental Medicine, Kyung Hee University Press, Seoul, Korea, 1996.
  17. E. B. Shim, S. Lee, J. Y. Kim, and Y. E. Earm, “Physiome and sasang constitutional medicine,” Journal of Physiological Sciences, vol. 58, no. 7, pp. 433–440, 2008. View at Publisher · View at Google Scholar · View at PubMed
  18. H. Chae, I. K. Lyoo, S. J. Lee, S. Cho, H. Bae, M. Hong et al., “An alternative way to individualized medicine: psychological and physical traits of Sasang typology,” Journal of Alternative and Complementary Medicine, vol. 9, pp. 519–528, 2003. View at Google Scholar
  19. J. R. Speakman, K. A. Rance, and A. M. Johnstone, “Polymorphisms of the FTO gene are associated with variation in energy intake, but not energy expenditure,” Obesity, vol. 16, no. 8, pp. 1961–1965, 2008. View at Publisher · View at Google Scholar · View at PubMed
  20. J. E. Cecil, R. Tavendale, P. Watt, M. M. Hetherington, and C. N. A. Palmer, “An obesity-associated FTO gene variant and increased energy intake in children,” New England Journal of Medicine, vol. 359, no. 24, pp. 2558–2566, 2008. View at Publisher · View at Google Scholar · View at PubMed
  21. N. J. Timpson, P. M. Emmett, T. M. Frayling et al., “The fat mass- and obesity-associated locus and dietary intake in children,” American Journal of Clinical Nutrition, vol. 88, no. 4, pp. 971–978, 2008. View at Google Scholar
  22. J. Wardle, S. Carnell, C. M. A. Haworth, I. S. Farooqi, S. O'Rahilly, and R. Plomin, “Obesity associated genetic variation in FTO is associated with diminished satiety,” Journal of Clinical Endocrinology and Metabolism, vol. 93, no. 9, pp. 3640–3643, 2008. View at Publisher · View at Google Scholar · View at PubMed
  23. E. Rampersaud, B. D. Mitchell, T. I. Pollin et al., “Physical activity and the association of common FTO gene variants with body mass index and obesity,” Archives of Internal Medicine, vol. 168, no. 16, pp. 1791–1797, 2008. View at Publisher · View at Google Scholar · View at PubMed
  24. A. Haupt, C. Thamer, J. Machann et al., “Impact of variation in the FTO gene on whole body fat distribution, ectopic fat, and weight loss,” Obesity, vol. 16, no. 8, pp. 1969–1972, 2008. View at Publisher · View at Google Scholar · View at PubMed
  25. T. D. Müller, A. Hinney, A. Scherag et al., “'Fat mass and obesity associated' gene (FTO): no significant association of variant rs9939609 with weight loss in a lifestyle intervention and lipid metabolism markers in German obese children and adolescents,” BMC Medical Genetics, vol. 9, article 85, 2008. View at Publisher · View at Google Scholar · View at PubMed
  26. N. Balthasar, L. T. Dalgaard, C. E. Lee et al., “Divergence of melanocortin pathways in the control of food intake and energy expenditure,” Cell, vol. 123, no. 3, pp. 493–505, 2005. View at Publisher · View at Google Scholar · View at PubMed
  27. J. C. Chambers, P. Elliott, D. Zabaneh et al., “Common genetic variation near MC4R is associated with waist circumference and insulin resistance,” Nature Genetics, vol. 40, no. 6, pp. 716–718, 2008. View at Publisher · View at Google Scholar · View at PubMed
  28. R. J. F. Loos, C. M. Lindgren, S. Li et al., “Common variants near MC4R are associated with fat mass, weight and risk of obesity,” Nature Genetics, vol. 40, no. 6, pp. 768–775, 2008. View at Publisher · View at Google Scholar · View at PubMed
  29. H. D. Shin, K. S. Kim, M. H. Cha, and Y. Yoon, “The effects of UCP-1 polymorphisms on obesity phenotypes among Korean female subjects,” Biochemical and Biophysical Research Communications, vol. 335, no. 2, pp. 624–630, 2005. View at Publisher · View at Google Scholar · View at PubMed
  30. S. H. Park, M. G. Kim, S. J. Lee, J. Y. Kim, and H. Chae, “emperament and character profiles of Sasang typology in an adult clinical sample,” Evidence-Based Complementary and Alternative Medicine. In press. View at Publisher · View at Google Scholar · View at PubMed
  31. S. H. Kim, B. H. Koh, and I. B. Song, “A study on the standardization of QSCCII (Questionnaire for the Sasang Constitution Classification II),” Journal of Korean Oriental Medicine, vol. 17, pp. 337–393, 1996. View at Google Scholar
  32. K. J. Livak, “Allelic discrimination using fluorogenic probes and the 5' nuclease assay,” Genetic Analysis, vol. 14, no. 5-6, pp. 143–149, 1999. View at Publisher · View at Google Scholar
  33. J. C. Barrett, B. Fry, J. Maller, and M. J. Daly, “Haploview: analysis and visualization of LD and haplotype maps,” Bioinformatics, vol. 21, no. 2, pp. 263–265, 2005. View at Publisher · View at Google Scholar · View at PubMed
  34. M. Stephens and P. Donnelly, “A comparison of bayesian methods for haplotype reconstruction from population genotype data,” American Journal of Human Genetics, vol. 73, no. 5, pp. 1162–1169, 2003. View at Publisher · View at Google Scholar · View at PubMed
  35. M. Stephens, N. J. Smith, and P. Donnelly, “A new statistical method for haplotype reconstruction from population data,” American Journal of Human Genetics, vol. 68, no. 4, pp. 978–989, 2001. View at Publisher · View at Google Scholar · View at PubMed
  36. S.-L. T. Normand, “Tutorial in biostatistics meta-analysis: formulating, evaluating, combining, and reporting,” Statistics in Medicine, vol. 18, no. 3, pp. 321–359, 1999. View at Google Scholar
  37. Q. Yang, J. Cui, I. Chazaro, L. A. Cupples, and S. Demissie, “Power and type 1 error rate of fales discovery rate approaches in genome-wide association studies,” BMC Genetics, vol. 6, supplement 1, no. 1, article S134, 2005. View at Publisher · View at Google Scholar · View at PubMed
  38. J. Y. Kim and H. Kim, “A statistical analysis of the distribution of Sasang constitutions in Iksan Wonkwang Oriental Medicine,” Journal of Korean Oriental Medicine, vol. 24, pp. 118–129, 2003. View at Google Scholar
  39. T. Gerken, C. A. Girard, Y.-C. L. Tung et al., “The obesity-associated FTO gene encodes a 2-oxoglutarate-dependent nucleic acid demethylase,” Science, vol. 318, no. 5855, pp. 1469–1472, 2007. View at Publisher · View at Google Scholar · View at PubMed