- Research article
- Open Access
- Open Peer Review
This article has Open Peer Review reports available.
Meta-analysis on the effect of the N363S polymorphism of the glucocorticoid receptor gene (GRL) on human obesity
- Amelia Marti†1Email author,
- M Carmen Ochoa†1,
- Almudena Sánchez-Villegas2, 3,
- J Alfredo Martínez1,
- Miguel Angel Martínez-González2,
- Johannes Hebebrand4,
- Anke Hinney4 and
- Helmut Vedder5
© Marti et al; licensee BioMed Central Ltd. 2006
Received: 14 October 2005
Accepted: 25 May 2006
Published: 25 May 2006
Since both excess glucocorticoid secretion and central obesity are clinical features of some obese patients, it is worthwhile to study a possible association of glucocorticoid receptor gene (GRL) variants with obesity. Previous studies have linked the N363S variant of the GRL gene to increased glucocorticoid effects such as higher body fat, a lower lean-body mass and a larger insulin response to dexamethasone. However, contradictory findings have been also reported about the association between this variant and obesity phenotypes. Individual studies may lack statistical power which may result in disparate results. This limitation can be overcome using meta-analytic techniques.
We conducted a meta-analysis to assess the association between the N363S polymorphism of the GRL gene and obesity risk. In addition to published research, we included also our own unpublished data -three novel case-control studies- in the meta-analysis The new case-control studies were conducted in German and Spanish children, adolescents and adults (total number of subjects: 1,117). Genotype was assessed by PCR-RFLP (Tsp509I). The final formal meta-analysis included a total number of 5,909 individuals.
The meta-analysis revealed a higher body mass index (BMI) with an overall estimation of +0.18 kg/m2 (95% CI: +0.004 to +0.35) for homo-/heterozygous carriers of the 363S allele of the GRL gene in comparison to non-carriers. Moreover, differences in pooled BMI were statistically significant and positive when considering one-group studies from the literature in which participants had a BMI below 27 kg/m2 (+ 0.41 kg/m2 [95% CI +0.17 to +0.66]), but the differences in BMI were negative when only our novel data from younger (aged under 45) and normal weight subjects were pooled together (-0.50 kg/m2 [95% CI -0.84 to -0.17]). The overall risk for obesity for homo-/heterozygous carriers of the 363S allele was not statistically significant in the meta-analysis (pooled OR = 1.02; 95% CI: 0.56–1.87).
Although certain genotypic effects could be population-specific, we conclude that there is no compelling evidence that the N363S polymorphism of the GRL gene is associated with either average BMI or obesity risk.
Since 1990, important efforts have been made to identify genes influencing complex traits, often by relying on the use of a priori selected candidate genes. According to the updated 2004 version of the Human Obesity Map, 113 candidate genes showed initial association with obesity, out of which only 18 genes are supported by at least five positive studies [1–3]. Since both excess glucocorticoid secretion and central obesity are clinical features of some obese patients, it is worthwhile to study a possible association of glucocorticoid receptor gene (GRL) variants with obesity [4, 5]. The GRL gene is located on chromosome 5q31.3 and is also named nuclear receptor subfamily 3, group C, member 1 (NR3C1). There are three known polymorphisms in the GRL gene -BclI, ER22/23EK, N363S- with the last two involved an aminoacid sequence change [6–17]. The N363S variant of the GRL gene increases the trans-activating capacity both in vivo e in vitro, and it has been shown to be associated with an increased sensitivity to glucocorticoids in vivo. An association of the variant N363S with measures of increased glucocorticoid effects such as more body fat, a larger insulin response to dexamethasone and a less lean-body mass has been reported [5, 7].
The polymorphism N363S (rs6195) in exon 2 of the GRL (U78506) is present with allele frequencies ranging from 0.7% in a South Asian population  to 27% in Australian subjects . This polymorphism was reported to be associated with an increased body mass index (BMI), an increased weight gain or a higher waist to hip ratio in some populations, i. e. in Dutch, Anglo-Celtic, French and Australian individuals [6, 7, 11, 15, 16], while other studies performed on Danish, Swedish, and South Asian subjects were not able to confirm this finding [9, 10, 12–14, 17]. The disparity of the results may partly be attributed to insufficient power in some of these studies, false positive or negative findings, or other reasons such as methodological issues, or the heterogeneity in age, sex, ethnic origin or average BMI of participants.
To further explore the role of the N363S polymorphism of the GRL gene in human obesity, we examined novel case-control data from two Spanish and one German study and included the results in a meta-analysis of a large number of previously published studies.
To overcome the limitations of the previous research work, we pooled data from different studies including our own results to rigorously assess any association and ascertain the likelihood and magnitude of the association between the allelic variants and the phenotype of interest [18–21]. Because non-significant results can be due to type 2 errors, meta-analyses greatly increase the power  and thus reduce the probability of false negative findings. On the other hand, some of the apparently significant results are simply due to type 1 errors resulting from spurious findings. Consequently, data pooling also reduces the type 1 error rate.
Therefore, we performed a meta-analysis by combining our data from three novel case-control studies (n = 1,117) with a number of previously reported studies (n = 4,792), to gain convincing evidence for (or against) the association between the N363S polymorphism of the GRL gene and obesity risk. A family-based study was also conducted in 124 German obesity trios (obese child or adolescent and both of their biological parents).
Phenotypic characteristics of the two Spanish case-control studies
Obese (n = 185)
Controls (n = 185)
Obese (n = 159)
Controls (n = 154)
BMI (kg/m 2 )
Percentage body fat
The German study of case-parents encompassed 124 extremely obese children and adolescents (BMI ≥ 99th BMI percentile according to German reference data  and both of their parents. It is worth mentioning that obese children and adolescents included in the case-parent study were independent of the individuals included in the case-control study. All participants of the German study groups were Caucasians recruited in West and South Germany.
The study was approved by the Ethics Committee of each University, and all subjects, (and, in case of minors, their parents) provided written informed consent. The reported investigation was carried out according to the principles of the Declaration of Helsinki II.
Extraction of genomic DNA was performed according to standard protocols. The N363S polymorphism of the GRL gene was analyzed by PCR-RFLP (digestion with Tsp509I) as described previously . For validity of the genotypes, allele determination was made independently by at least two experienced individuals. Discrepancies were solved unambiguously either by reaching consensus or by repeating the experimental procedure. In addition, we checked for Mendelian inconsistencies in the trios with the program Pedcheck .
Descriptive values are given as mean and standard error of the mean. Univariate statistical analysis was performed using unpaired Student t-test and Chi square test (for frequencies).
The Transmission-Disequilibrium Test (TDT) was used to assess the differential pattern of excess transmission of alleles from heterozygous parents to diseased children . By sampling family trios including the affected children and adolescents (probands), the association between N363S allele and obesity would lead to a transmission type different from the expected probability of 0.5. When cases are unrelated probands, TDT represents a valid test of association, even if a population stratification is present .
To systematically review differences in BMI across the presence/absence of the N363S polymorphism of the GRL gene (including homozygous and heterozygous subjects for the 363S allele together) we used a formal meta-analysis . Procedures of formal meta-analysis have been mostly applied to combine the results from previously reported studies. However, in the current meta-analysis, we also included data from three of our own studies that have not been published yet.
A Pubmed search revealed 16 studies published before April 2005 focusing on the analysis of the N363S polymorphism of the GRL gene in human (obese or lean) subjects. Subsequently, these were included in the present analysis. Since new information was required on the frequencies of the N363S polymorphism of the GRL gene according to different BMI categories, we personally contacted all authors to obtain additional information by personal communication (12 of the 16 studies). Therefore, we were able to combine data from 12 studies with a total of 4,792 subjects from the literature and data from our present investigation on 1,117 subjects. Thus, the total number of subjects in the meta-analysis was 5,909 subjects.
The meta-analysis provides a logical structure for systematically quantifying evidence and for exploring bias and diversity in research. In our meta-analysis, the presence/absence of the polymorphism was considered as the exposure, whereas a change in BMI was considered as the outcome. The average difference in BMI between individuals with or without the N363S polymorphism (homo-/heterozygous carriers of the 363S allele vs. non-carriers) of the GRL gene was used as the outcome.
We estimated a summary difference (ds) as the weighted effect size :
d s = d i w i w i
ds is the pooled estimate across studies for the difference in the BMI (kg/m2) in homo-/heterozygous carriers and non-carriers of 363Ser allele, wi is the weight assigned to each study (wi is the inverse of the variance for the difference in BMI found in each study) and di is the BMI difference between those with or without the N363S polymorphism in each individual study. We also calculated a 95% confidence interval (CI) for the pooled difference in BMI:
95% CI = d s ± (1.96 × SE)
where SE is the standard error of the pooled estimate .
A test of heterogeneity was also calculated, estimating a Q statistic, which follows a Chi-square distribution with degrees of freedom of k-1, k being the number of studies included in the analysis. A two-tailed p value < 0.05 for this statistic parameter indicates the presence of heterogeneity, which somewhat compromises the validity of the pooled estimates . For the pooled odds ratio we used the DerSimonian and Laird's random effect model .
Because significant heterogeneity was clearly evident in the pooled difference estimates for all studies combined, we evaluated potential sources of heterogeneity by subset analysis . We analysed sub-groups using the following criteria: firstly, unpublished studies which included six datasets from the present investigation considering obese and control subjects and children and adolescents vs. adult subjects; secondly, published studies with one population group (nine studies); thirdly, published studies with two groups – an obese and a lean subject group (three studies, six datasets). We also repeated the meta-analysis in subgroups built according to the prevalence of the mutation -homo-/heterozygous carriers- (<5%; 5–10%: >10%), according to ethnicity, and according to the gender of participants.
Studies on Spanish and German populations
In this work, firstly we examined the N363S polymorphism of the GRL gene in two Spanish case-control studies. The main phenotypic characteristics of the Spanish adults and children study groups are given in Table 1. The German population was composed of 178 extremely obese children and adolescents (mean age 14, 50% boys) and 256 lean young adults (mean age 25, 50% male) as indicated in the Methods section.
Mean and difference (95% CI) in body mass index (kg/m2) between individuals homozygous and heterozygous carriers of the 363S allele of the GRL gene and homozygotes for the N363 allele in studies with two population group
Normal weight subjects
Lin et al. 1999
Lin et al. 2003
Echwald et al. 2001
Children and adolescents
Apart from these three study groups, a family-based association study was also conducted separately in 124 German trios. 15 parents were heterozygous for the N363S polymorphism of the GRL gene, of which 8 transmitted the allele 363S (p-value = 0.99). Hence, we detected no transmission disequilibrium for the N363S polymorphism of the GRL gene in the population studied.
Published studies included in the meta-analysis
Mean and difference (95% CI) in body mass index (kg/m2) between individuals homozygous and heterozygous carriers of the 363S allele of the GRL gene and homozygotes for the N363 allele in studies with one population group
Isle of Ely, UK
South Asian, UK
Pooled differences (95% CI) in body mass index (kg/m2) between individuals homozygous and heterozygous carriers of the 363S allele of the GRL gene and homozygotes for the N363 allele. Fixed effects model
Difference in BMI (kg/m2) Pooled estimates
+0.004 to +0.35*
BMI < 27 kg/m2
-0.052 to +0.32
BMI > 27 kg/m2
-0.047 to +0.79
Adults (>25 years)
+0.31 to +0.72*
Children and adolescents (<25 years)
-0.99 to -0.35*
-0.01 to +0.34
-0.34 to +1.24
-1.25 to +0.51
Men and women
+0.02 to +0.37
- Mutation prevalence
-0.96 to -0.12
+0.15 to +0.54
-0.57 to +0.77
BMI < 27 kg/m2
+0.17 to +0.66*
BMI ≥ 27 kg/m2
+0.64 to +1.74*
Normal weight subjects
already published data
-0.07 to +1.19
-0.84 to -0.17*
already published data
-0.82 to +1.46
-2.10 to -0.49*
When analyzing data from one-population studies (Table 4), a subgroup of four studies was generated considering only reports including participants with BMI values below 27 kg/m2. For this group, the pooled difference in BMI values was statistically significant (+0.41 kg/m2; [95% CI: +0.17 to +0.66]) for 363S homo-/heterozygous carriers of the 363S allele compared to non-carriers.
We also examined the pooled difference in BMI between homo-/heterozygous carriers and non-carriers of the 363S allele of the GRL gene in published articles with two population groups: a group of controls (normal weight subjects) and a group of cases (obese subjects). The pooled difference in BMI between homo-/heterozygous carriers and non-carriers of the 363 allele was not statistically significant when studies with normal weight subjects (+0.56 kg/m2; [95% CI: -0.072 to +1.19]) and obese subjects (+0.32 kg/m2 [95% CI: -0.82 to +1.46]) were considered separately. However, the pooled difference in BMI was negative and statistically significant in homo-/heterozygous carriers of the S363 allele when only novel data for normal weight subjects were examined (-0.50 kg/m2; [95% CI: -0.84 to -0.17]). Opposite tendencies for differences in BMI were also found when performing the meta-analysis after stratifying by gender, prevalence of the polymorphism and considering children and adult populations, separately (Table 4).
The present study was aimed to assess the effect of the N363S polymorphism of the GRL gene on the incidence of obesity. Although procedures of meta-analyses have mostly been applied to comprehensively examine the results from previously reported studies, we here also include novel data from three studies derived from Spanish and German populations of our group that have not been published so far. Moreover, the meta-analysis was performed only after relevant data that were not available in the original publications were obtained contacting directly with the authors. The new data set was generated using two different strategies: the first was to match controls to cases by gender and age, whereas the second one was performed as a case-parent study that can be considered as a special type of case-control study in which cases (unrelated probands) and pseudocontrols (parental non-transmitted alleles) are matched by ethnic origin. The magnitude of the association can be assessed by odds ratios (OR) in the case-control study, while the deviations of the transmission probabilities from the expected value under the null hypothesis of no-association (50%) are related to the genotype relative risk . The close proximity of point estimates for ORs (Figure 3) with values below 1.0 and the transmission probabilities found in the case-parent study do not suggest a positive association between the N363S polymorphism of the GRL gene and childhood obesity in the German population.
We further addressed the general prevalence of the N363S polymorphism of the GRL gene and found it to be slightly more frequent in the German than in the Spanish study groups. Across populations, the genotype frequency of the polymorphism of the GRL gene varies widely. In Europe, it ranges from 4% to 6% for homo-/heterozygous carriers of the 363S allele in German, Spanish, French or British subjects and between 9% and 15% in Swedish and Danish individuals [6, 10, 11, 14, 17] Australian populations have higher frequencies of homo-/heterozygous carriers of the 363S-allele, ranging from 12–13% in normal weight individuals to 26–27% in obese subjects (Tables 2 and 3; [12, 15, 16]). There are also important differences in the genotype frequency of the polymorphism in obese and non-obese subjects in several other populations. Surprisingly, for the Spanish and German normal weight groups, the number of homo-/heterozygous carriers of the 363S allele of the GRL gene was higher compared to that found in obese subjects of the same population groups (Table 3).
To confirm the strength of our findings and because inconsistent data have been reported on the relationship between the N363S polymorphism of the GRL gene and obesity phenotypes [33, 34], after adding our own new data to previously published results, data from 5,909 unrelated subjects from a diverse ethnic backgrounds were pooled together for the analysis of BMI differences between homo-/heterozygous carriers and non-carriers of the 363S allele of the GRL gene. The overall pooled estimated genotype frequency for homo-/heterozygous carriers of the 363S allele was 4.47% (95% CI: 4.24–5.30) with a substantial heterogeneity (p < 0.001). Interestingly, for BMI differences, the overall estimation was +0.18 kg/m2 (95% CI: +0.004 to +0.35) higher in homo-/heterozygous carriers of 363S allele of the GRL gene than in non-carriers, also with an important heterogeneity (p < 0.001). It is worthwhile to mention that the pooled analysis (i.e. the "one population studies") revealed a large range for BMI: from non-obese (mean BMI = 21.1 kg/m2, ref. 14) to severely-obese individuals (mean BMI = 41.7 kg/m2, ref 11) and also with regard to age: from 18 years  to 66–68 years . Moreover, three studies were only conducted with men [9, 10, 14], while four studies included male and female subjects [6, 7, 11, 13]. Disparities in BMI across studies as well as age and sex variability may at least partly account for the observed heterogeneity (Table 2).
Interestingly, when a subgroup of data was generated considering only reports whose participants showed a BMI below 27 kg/m2, the pooled difference in BMI values for homo-/heterozygous carriers of the 363S allele vs. non-carriers was statistically significant and homogeneous (+0.41 kg/m2; 95% CI: +0.17 to +0.66) with a p-value for heterogeneity of 0.12. Funnel plots of effect estimates (differences in BMI) against sample size showed symmetrical distribution suggesting that there was no apparent publication bias in the available studies.
With regard to the meta-analysis, a drawback of the OR analysis is the use of different criteria to define obese and non-obese individuals in the various studies. Some examinations (e.g. Echwald et al. 2001, and Navarra studies) were based on rather low BMI thresholds for obesity, whereas others included morbidly-obese patients with BMI values well above 35 kg/m2. Moreover, there are important differences in age and sex among the groups analysed. Because the respective information was not provided in all studies, age and sex effects could not be adequately addressed in the current meta-analysis.
Two groups of children and adolescents (boys and girls) were included in the German and Spanish studies as well as one large group of young men with a mean age of about 27 years . The other three studies were conducted in adults. In two studies [15, 16], the criteria for age and percentage of males were quite similar -an age range of 48–52 years and a percentage of 49–57% of males- while in the third, the mean age of subjects was different (39–42 years old) as was the percentage of males (12–26%, Table 1).
Overall, our analyses did not indicate an increased risk for the development of obesity for homo-/heterozygous carriers of the S363 allele of the GLR as shown by a pooled OR of 1.02 (95% CI: 0.56–1.87). Interestingly, an inverse association (OR = 0.45) was obtained after pooling the German and Spanish studies for homo-/heterozygous carriers of the 363S allele compared to non-carriers, suggesting population differences for this parameter. Beyond the already mentioned limitations of our meta-analysis, our study provides a sound base for the further investigation on the role of the polymorphism N363S of the GRL gene in large population samples of diverse ethnic origins . It also yields a much better opportunity for the detection of significant effects in sub-group analyses of homogeneous data. Thus, the meta-analysis represents a useful strategy to assess the potential contribution of variants with rather low allele frequencies (i.e. the N363S polymorphism of the GRL from 4 to 9%), which may exert only moderate effects on polygenic disorders.
Although certain genotypic effects could be population-specific, we conclude that there was no compelling evidence that the N363S polymorphism of the GRL gene is associated with the average BMI or with an increased prevalence of obesity, in the large number of human studies included in our analyses.
The authors are grateful for the participation of subjects and their families, the contributions of the participants and authors of the studies from the literature used for the meta-analysis and the collaboration of GENOI members (Azcona C, Patiño A, Chueca M, Oyarzabal M, Pelach R, Berrade S, Gainza R, Moreno-Aliaga MJ) as well as Forga, L and Corbalan MS. This work was supported by grants for the Navarra Government and Línea Especial (University of Navarra). We are grateful for the excellent technical assistance of Veronica Ciauriz, Gerti Gerber and Ana Lorente. The study was supported by grants of the BMBF (NGFN1 and 2; 01GS0118 and 01GS0482).
- Bell CG, Walley AJ, Froguel P: The genetics of human obesity. Nat Rev Genet. 2005, 6: 221-234. 10.1038/nrg1556.View ArticlePubMedGoogle Scholar
- Perusse L, Rankinen T, Zuberi A, Chagnon YC, Weisnagel SJ, Argyropoulos G, Walts B, Snyder EE, Bouchard C: The human obesity gene map: the 2004 update. Obes Res. 2005, 13: 381-490.View ArticlePubMedGoogle Scholar
- Marti A, Moreno-Aliaga MJ, Hebebrand J, Martinez JA: Genes, lifestyles and obesity. Int J Obes Relat Metab Disord. 2004, 28 Suppl 3: S29-36. 10.1038/sj.ijo.0802808.View ArticlePubMedGoogle Scholar
- Rosmond R: The glucocorticoid receptor gene and its association to metabolic syndrome. Obesity research. 2002, 10: 1078-1086.View ArticlePubMedGoogle Scholar
- Van Rossum EF, Lamberts SW: Polymorphisms in the glucocorticoid receptor gene and their associations with metabolic parameters and body composition. Recent Prog Horm Res. 2004, 59: 333-357. 10.1210/rp.59.1.333.View ArticlePubMedGoogle Scholar
- Roussel R, Reis AF, Dubois-Laforgue D, Bellanne-Chantelot C, Timsit J, Velho G: The N363S polymorphism in the glucocorticoid receptor gene is associated with overweight in subjects with type 2 diabetes mellitus. Clin Endocrinol (Oxf). 2003, 59: 237-241. 10.1046/j.1365-2265.2003.01831.x.View ArticleGoogle Scholar
- Huizenga N, Koper JW, de Lange P, Pola H, Stolk R, Burger H, Grobbee DE, Brinkmann AO, de Jong FH, Lamberts S: A polymorphism in the glucocorticoid receptor gene may be associated with an increased sensitivity to glucocorticoids in vivo. The journal lf clinical endocrinology and metabolism. 1998, 83: 144-151. 10.1210/jc.83.1.144.Google Scholar
- Halsall D, Luan J, Hales N, Wareham NJ, O´Railly S: Rapid Response. Glucocorticoid receptor variant and body mass index. BMJ [htpp://bmjcom/elettrers/ 319/7221/1337]. 2000Google Scholar
- Rosmond R, Bouchard C, Bjorntorp P: Tsp509I polymorphism in exon 2 of the glucocorticoid receptor gene in relation to obesity and cortisol secretion: cohort study. BMJ. 2001, 322: 652-653. 10.1136/bmj.322.7287.652.View ArticlePubMedPubMed CentralGoogle Scholar
- Rosmond R: Letter: Glucocorticoid receptor N363S variant in obesity: comes into vanity and goes into darkness. Obesity research. 2003, 11: 1606-1607.View ArticlePubMedGoogle Scholar
- Dobson MG, Redfern CPF, Unwin N, Weaver JU: The N363S polymorphism of the glucocorticoid receptor: potential contribution to central obesity in men and lack of association with other risk factors for coronary heart disease and diabetes mellitus. Journal of clinical endocrinology and metabolism. 2001, 86: 2270-2274. 10.1210/jc.86.5.2270.PubMedGoogle Scholar
- Morris BJ, Lin RC, Wang XL, Dalziel B, Caterson ID: Response: Central Obesity Is Associated with Glucocorticoid Receptor N363S Variant: Big Picture Sheds Light. Obesity Research. 2003, 11: 1607-1069.View ArticleGoogle Scholar
- Syed AA, Irving J, Redfern C, Hall AG, Unwin NC, White M, Bhopal RS, Alberti K, Weaver JU: Low prevalence of the N363S polymorphism of the glucocorticoid receptor in South Asians living in the United kingdom. The journal lf clinical endocrinology and metabolism. 2004, 89: 232-235. 10.1210/jc.2003-030995.View ArticleGoogle Scholar
- Wust S, Van Rossum EF, Federenko IS, Koper JW, Kumsta R, Hellhammer DH: Common polymorphisms in the glucocorticoid receptor gene are associated with adrenocortical responses to psychosocial stress. J Clin Endocrinol Metab. 2004, 89: 565-573. 10.1210/jc.2003-031148.View ArticlePubMedGoogle Scholar
- Lin RC, Wang WY, Morris BJ: High penetrance, overweight, and glucocorticoid receptor variant: case-control study. Bmj. 1999, 319: 1337-1338.View ArticlePubMedPubMed CentralGoogle Scholar
- Lin RCY, Wang XL, Dalziel B, Caterson ID, Morris DJ: Association of obesity, but not diabetes or hypertension, with glucocorticoids receptor N363S variant. Obesity Research. 2003, 11: 802-808.View ArticlePubMedGoogle Scholar
- Echwald SM, Sorensen TI, Andersen T, Pedersen O: The Asn363Ser variant of the glucocorticoid receptor gene is not associated with obesity or weight gain in Danish men. Int J Obes Relat Metab Disord. 2001, 25: 1563-1565. 10.1038/sj.ijo.0801744.View ArticlePubMedGoogle Scholar
- Geller F, Reichwald K, Dempfle A, Illig T, Vollmert C, Herpertz S, Siffert W, Platzer M, Hess C, Gudermann T, Biebermann H, Wichmann HE, Schafer H, Hinney A, Hebebrand J: Melanocortin-4 receptor gene variant I103 is negatively associated with obesity. Am J Hum Genet. 2004, 74: 572-581. 10.1086/382490.View ArticlePubMedPubMed CentralGoogle Scholar
- Masud S, Ye S: Effect of the peroxisome proliferator activated receptor-gamma gene Pro12Ala variant on body mass index: a meta-analysis. J Med Genet. 2003, 40: 773-780. 10.1136/jmg.40.10.773.View ArticlePubMedPubMed CentralGoogle Scholar
- Lohmueller KE, Pearce CL, Pike M, Lander ES, Hirschhorn JN: Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease. Nat Genet. 2003, 33: 177-182. 10.1038/ng1071.View ArticlePubMedGoogle Scholar
- Heo M, Leibel RL, Fontaine KR, Boyer BB, Chung WK, Koulu M, Karvonen MK, Pesonen U, Rissanen A, Laakso M, Uusitupa MI, Chagnon Y, Bouchard C, Donohoue PA, Burns TL, Shuldiner AR, Silver K, Andersen RE, Pedersen O, Echwald S, Sorensen TI, Behn P, Permutt MA, Jacobs KB, Elston RC, Hoffman DJ, Gropp E, Allison DB: A meta-analytic investigation of linkage and association of common leptin receptor (LEPR) polymorphisms with body mass index and waist circumference. Int J Obes Relat Metab Disord. 2002, 26: 640-646. 10.1038/sj.ijo.0801990.View ArticlePubMedGoogle Scholar
- Ochoa MC, Marti A, Azcona C, Chueca M, Oyarzabal M, Pelach R, Patino A, Moreno-Aliaga MJ, Martinez-Gonzalez MA, Martinez JA: Gene-gene interaction between PPAR gamma 2 and ADR beta 3 increases obesity risk in children and adolescents. Int J Obes Relat Metab Disord. 2004, 28 Suppl 3: S37-41. 10.1038/sj.ijo.0802803.View ArticlePubMedGoogle Scholar
- Corbalan MS, Marti A, Forga L, Martinez-Gonzalez MA, Martinez JA: The risk of obesity and the Trp64Arg polymorphism of the beta(3)-adrenergic receptor: effect modification by age. Ann Nutr Metab. 2002, 46: 152-158. 10.1159/000063084.View ArticlePubMedGoogle Scholar
- Hebebrand J, Himmelmann GW, Heseker H, Schafer H, Remschmidt H: Use of percentiles for the body mass index in anorexia nervosa: diagnostic, epidemiological, and therapeutic considerations. Int J Eat Disord. 1996, 19: 359-369. 10.1002/(SICI)1098-108X(199605)19:4<359::AID-EAT4>3.0.CO;2-K.View ArticlePubMedGoogle Scholar
- O'Connell JR, Weeks DE: PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet. 1998, 63: 259-266. 10.1086/301904.View ArticlePubMedPubMed CentralGoogle Scholar
- Schaid DJ: Transmission disequilibrium, family controls, and great expectations. Am J Hum Genet. 1998, 63: 935-941. 10.1086/302077.View ArticlePubMedPubMed CentralGoogle Scholar
- Greenland S: Meta-analysis. Modern Epidemiology. Edited by: Greenland KJRS. 1998, Philadelphia, PA, Lippincott Raven, 643-673.Google Scholar
- Dickersin K: Systematic reviews in epidemiology: why are we so far behind?. Int J Epidemiol. 2002, 31: 6-12. 10.1093/ije/31.1.6.View ArticlePubMedGoogle Scholar
- Hedges LV: Estimation of effect size from a series of independent experiments. Psychol Bull. 1982, 92: 490-499. 10.1037//0033-2909.92.2.490.View ArticleGoogle Scholar
- Takkouche B, Cadarso-Suarez C, Spiegelman D: Evaluation of old and new tests of heterogeneity in epidemiologic meta-analysis. Am J Epidemiol. 1999, 150: 206-215.View ArticlePubMedGoogle Scholar
- DerSimonian R, Laird N: Meta-analysis in clinical trials. Control Clin Trials. 1986, 7: 177-188. 10.1016/0197-2456(86)90046-2.View ArticlePubMedGoogle Scholar
- Schaid DJ: Likelihoods and TDT for the case-parents design. Genet Epidemiol. 1999, 16: 250-260. 10.1002/(SICI)1098-2272(1999)16:3<250::AID-GEPI2>3.0.CO;2-T.View ArticlePubMedGoogle Scholar
- Buemann B, Black E, Holst C, Toubro S, Echwald S, Pedersen O, Astrup A, Sorensen T: The N363S polymorphism of the glucocorticoid receptor and metabolic syndrome factors in men. Obes Res. 2005, 13: 862-867.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-2350/7/50/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.