- Research article
- Open Access
A genome-wide scan for type 1 diabetes susceptibility genes in nuclear families with multiple affected siblings in Finland
BMC Genetics volume 8, Article number: 84 (2007)
A genome-wide search for genes that predispose to type 1 diabetes using linkage analysis was performed using 900 microsatellite markers in 70 nuclear families with affected siblings from Finland, a population expected to be more genetically homogeneous than others, and having the highest incidence of type 1 diabetes in the world and, yet, the highest proportion in Europe of cases (10%) carrying neither of the highest risk HLA haplotypes that include DR3 or DR4 alleles.
In addition to the evidence of linkage to the HLA region on 6p21 (nominal p = 4.0 × 10-6), significant evidence of linkage in other chromosome regions was not detected with a single-locus analysis. The two-locus analysis conditional on the HLA gave a maximum lod score (MLS) of 3.1 (nominal p = 2 × 10-4) on chromosome 9p13 under an additive model; MLS of 2.1 (nominal p = 6.1 × 10-3) on chromosome 17p12 and MLS of 2.5 (nominal p = 2.9 × 10-3) on chromosome 18p11 under a general model.
Our genome scan data confirmed the primary contribution of the HLA genes also in the high-risk Finnish population, and suggest that non-HLA genes also contribute to the familial clustering of type 1 diabetes in Finland.
Type 1 diabetes is the third most prevalent chronic disease of childhood, affecting 0.4% of the general population by age of 30 years and has a lifetime risk of nearly 1% [1, 2]. The incidence of type 1 diabetes varies very significantly between populations [1, 3–6]. A 30-fold difference in type 1 diabetes risk has been detected worldwide with the highest incidence of the disease in Finland and the lowest incidence of the disease in Asia [4–7]. The etiology of type 1 diabetes is unknown, but it is recognized to be due to both genetic and environmental determinants [8, 9].
The observation of familial clustering of type 1 diabetes suggests that genetic factors are involved in the etiology of type 1 diabetes. For people of European ancestry, the frequency of type 1 diabetes in siblings of affected individuals is about 6% by the age of 30 [10, 11], while the frequency in the general population is about 0.4–0.5% by the age of 30 . Thus, type 1 diabetes is about 15 times (6/0.4) more common in siblings of type 1 diabetic patients than in the general population. The risk of type 1 diabetes increased also in the offspring of diabetic patients, to about 3–6% . The concordance rate for type 1 diabetes has been found to be higher in monozygotic (MZ, 100% shared genes) than in dizygotic (DZ, average 50% shared genes) twins, with cumulative MZ rates approximately 35–50% [13–18]. The population-based Finnish  and Danish  studies have revealed that genetic factors may contribute approximately 75–80% of the liability to type 1 diabetes. The high discordance between MZ twins, however, suggests that the penetrance of the type 1 susceptibility genes is low.
Following the lead from gene identification studies in rare Mendelian diseases and the clear evidence of linkage of the MHC in human and mouse to type 1 diabetes, genome-wide scans for linkage to type 1 diabetes were undertaken [19–26]. These studies all confirmed the importance of HLA-encoded susceptibility to type 1 diabetes (designated also as IDDM1); and also excluded the possibility of a locus with an effect equivalent to HLA. The individual impact of other susceptibility genes is, therefore, much smaller than that of HLA. Nevertheless, statistically significant and suggestive evidence of linkage of type 1 diabetes to at least ten chromosome regions has been published, although association studies at INS  and CTLA4 have been required to confirm with fine map loci. These newly identified susceptibility loci showed evidence for linkage in some studies but could not be replicated in others. The discrepancies between the studies may be due to a number of factors, including sample size, genetic and phenotypic heterogeneity between data sets, genotyping methods, gender-specific effects and genetic epistasis [12, 28]. We are now reporting here the first genome scan results using microsatellite markers among Finnish nuclear families with at least two siblings affected with type 1 diabetes. Finland is known to have a high degree of population homogeneity genetically, compared with most other countries because it has a distinct founder population. Finnish type 1 diabetic patients have a high frequency of non-DR3, non-DR4 positive HLA haplotypes (approximately 10%), suggesting the possibility that non-HLA loci, perhaps with a reasonable penetrance and population allelic frequency due to founder effects exists in Finland.
A total of 868 loci with a length of 3518 cM were actually genotyped. Figures 1, 2, 3 show the MLS curves generated using a single-locus analysis or a two-locus analysis fitted under additive and general models for the action of the two loci. The highest MLS was at chromosome 6p21, the HLA region where the major type 1 diabetes susceptibility gene(s) locates. For the two-locus analysis, we fixed markers with highest MLS at the HLA region to adjust for the effect of HLA. Then the joint IBD sharing at the HLA locus and at a second locus was considered, which was placed at an increment of 1.0 cM across the genome. The MLS for the effect of HLA was subtracted so that the curves in figures represent the additional contribution of locus 2. As expected, at positions unlinked to HLA such as those on different chromosomes, the multiplicative curves were identical to those curves obtained by use of a single-locus model for locus 2 and therefore were not presented in the figures.
For a single-locus analysis, a MLS of 4.67 (nominal p = 4.0 × 10-6) at chromosome 6p21 (HLA region) was observed. Another region, on 9p13 shows a MLS of 3.09 under either a two-locus additive model (nominal p = 2 × 10-4) or general model (nominal p = 4 × 10-4). Two other regions on 17p12 and 18p11 showed positive findings under two-locus general model (Table 1), with MLS of 2.1 and 2.5, respectively (which remains suggestive even after the Bonferroni correction for the three tests performed – single/multiplicative, additive and general – is applied).
Joint IBD sharing probabilities for an affected sibling pair to share 0, 1 or 2 alleles IBD at 6p21 and each additional locus under a general model are shown in Table 2.
Our study of Finnish affected sib-pairs with type 1 diabetes provides further evidence showing that the genes in the HLA region are of the primary importance in this high-risk population. Nevertheless, our results also add to the evidence that there are non-HLA loci with suggestive evidence of linkage to three chromosome regions: 9p13, 17p12 and 18p11.
Recently, new methods to carry out whole-genome association study using a large number of single nucleotide polymorphisms (SNPs) have become available. 18p11 has been reported to have robust association in the first genome-wide association study in type 1 diabetes along with several other loci showing a significant association . The evidence of linkage to the chromosome 18p11 in our study was, however, modest, which might provide a support to the findings from the above cited study or be a mere chance. In a large study of 1435 multiplex families the genome-wide linkage analysis of type 1 diabetes found linkage in none of the three non-HLA loci as we did [19–26]. Taking into account the small sample size of our current study, we need to be cautious when interpreting our findings.
Current genotyping data originally was used to map loci for nephropathy selecting for statistical analysis only sib-pairs discordant (DSPs) for diabetic nephropathy . For DSPs, linked markers will be characterized by diminished, as opposed to excessive, allele sharing between sibs . Therefore, the lod score peak at 6p21 in affacted sib-pairs with type 1 diabetes, for example, was not revealed in the same region in the DSPs analysis when diabetic nephropathy was considered as the phenotype of interest. This suggests that the findings in the current study were not biased by the presence of nephropathy. However, the findings need to be further examined. The significance of our study is that we reconfirm the major significance of HLA genes and suggest that a linkage to chromosome 18p11 region might exist in this population with the highest risk of type 1 diabetes in the world.
Our genome scan data confirmed the primary contribution of the HLA genes also in the high-risk Finnish population, and suggest that non-HLA genes also contribute to the familial clustering of type 1 diabetes in Finland.
Patients and families
DNA from 70 Finnish nuclear families with at least two siblings affected with type 1 diabetes, including six families with three and one family with four affected children was collected from Finland. MODY families were not included. A total of 207 individuals (147 sibs and 60 parents) were genotyped, providing with 81 sib-pairs affected with type 1 diabetes for linkage analysis. The original study design was to collect DSPs, siblings affected with type 1 diabetes but discordant for diabetic nephropathy, to map loci for diabetic nephropathy. Therefore, all collected sib-pairs were affected with type 1 diabetes and in each family at least one sibling was affected with nephropathy. All sib-pairs were patients with type 1 diabetes receiving insulin treatment since the onset of the disease. In all affected sib-pairs the first patient was diagnosed before the age of 18 years. Since the patients were ascertained through the national data bases and many of them were diagnosed in the 1970s or the early 1980s, detailed clinical or biochemical data at diagnosis were not available. There is however little doubt that the diabetic patients would have other type of diabetes than type 1. The mean (SD) age at onset of type 1 diabetes in the 147 siblings was 14.5 (10.4) years, ranging from 1.2–53.4 years. Informed consent was obtained from all patients and their parents whose DNA samples were collected. The study was approved by the Ethical Committees of the Finnish National Public Health Institute, Helsinki, Finland and the Karolinska Institute, Stockholm, Sweden.
DNA was extracted from peripheral lymphocytes, according to standard procedures. A genome wide scan was performed using 900 microsatellite markers and using protocols described by Gretarsdottir et al. at the genotyping laboratory of deCODE Genetics, Reykjavik, Iceland. Information of the microsatellite markers and marker positions were obtained from the Marshfield genetic map (Center for Medical Genetics, Marshfield Medical Research Foundation). In the marker set used in this study, the average spacing between markers was ~4 cM, with no gap > 10 cM. Standard PCR techniques with fluorescently labeled primers were used to amplify polymorphic DNA fragments. The PCR products were supplemented with the internal size standard, separated and detected on an Applied Biosystems model 377 Sequencer by use of Genescan version 3.0 peak-calling software. Alleles were called automatically with TrueAllele program (Cybergenetics) and the deCodeGT program was used to fractionate according to quality and to edit the called genotypes .
A generalization of maximum lod score (MLS) method proposed by Risch  was used to assess the linkage in all affected sib-pairs of each pedigree, which is based on the measurement of the number of alleles (0,1,2) shared identical by descent (IBD) by two affected sibs at a locus. Genehunter (Version 2.0) was first used to estimate a single-locus MLS. We report the nominal p-values for the genome-wide single-locus analysis and note that in order to control family-wise error rate (FWER) one could apply Lander-Kruglyak critical value to obtain adjusted p-value. Nominal p-values in the range of 10-4 were considered a statistically significant threshold for linkage . Threshold MLS-LOD score values at 1.9 and 3.3 were considered for "suggestive" and "significant" linkage, respectively .
Two-locus analysis with Risch's method developed via an extension of the method by Cordell [37, 38] was then used to estimate the MLS at either a single locus or a second locus conditional on the HLA region, where the single-locus MLS was greatest. The null hypothesis for a two-locus analysis is that the locus 2 is not involved in disease, and the results are given for a variety of two-locus models, each fitted with the second locus placed at increments of 1.0 cM across the genome. The multiplicative model estimates the conditional MLS at locus 2, taking account of any effect at locus 1. If loci 1 and 2 are unlinked, the multiplicative conditional MLS for locus 2 will be identical to the single locus MLS for locus 2. The additive and general models calculate the conditional MLS at locus 2 taking account of any effect at locus 1, assuming an additive model for the joint action of loci 1 and 2, or allowing for arbitrary epistasis between loci 1 and 2 in the general model. Significance levels (nominal p values) for a single-locus MLS were calculated according to the possible triangle constraints described by Holmans  and for two-locus MLS generated for this particular data set analyzed using simulation .
To calculate the two-locus MLS, a prior as well as a posterior probability that each affected sib-pair shares i alleles IBD (i = 0,1,2) at particular positions on the genome is required. For unlinked loci, the IBD probabilities were obtained from the output of Genehunter (version 2.0) [40, 41] and for the linked loci on chromosome 6 they were generated allowing for separate male and female recombination fractions using MERLIN . A single-locus MLS for X chromosome was estimated using MAPMAKER/SIBS (version 2.0).
We also estimated the power of our sample to test for linkage using the mean IBD sharing test  by computer simulations. Depending on the degree of marker informativity assumed, we estimate that we have 56–72% power to detect at p value 0.01 a locus accounting for a sibling relative risk of 1.8, but only 33–41% to detect a locus accounting for a sibling relative risk of 1.5. The power to detect a locus-specific sibling relative risk of 1.8 at p value 0.001 is also less than 40%. This study clearly has limited power to detect loci of small effect, but it is encouraging that we have found suggestive evidence of linkage at three loci in addition to the significant linkage on 6p21.
Rewers M, LaPorte RE, King H, Tuomilehto J: Trends in the prevalence and incidence of diabetes: insulin-dependent diabetes mellitus in childhood. World Health Stat Q. 1988, 41 (3-4): 179-189.
Spielman RS, Baker L, Zmijewski CM: Gene dosage and suceptibility to insulin-dependent diabetes. Ann Hum Genet. 1980, 44 (Pt 2): 135-150. 10.1111/j.1469-1809.1980.tb00954.x.
Diabetes Epidemiology Research International Group: Geographic patterns of childhood insulin-dependent diabetes mellitus. Diabetes Epidemiology Research International Group. Diabetes. 1988, 37 (8): 1113-1119. 10.2337/diabetes.37.8.1113.
Karvonen M, Viik-Kajander M, Moltchanova E, Libman I, LaPorte R, Tuomilehto J: Incidence of childhood type 1 diabetes worldwide. Diabetes Mondiale (DiaMond) Project Group. Diabetes Care. 2000, 23 (10): 1516-1526. 10.2337/diacare.23.10.1516.
Karvonen M, Tuomilehto J, Libman I, LaPorte R: A review of the recent epidemiological data on the worldwide incidence of type 1 (insulin-dependent) diabetes mellitus. World Health Organization DIAMOND Project Group. Diabetologia. 1993, 36 (10): 883-892. 10.1007/BF02374468.
The DIAMOND Project Group: Incidence and trends of childhood Type 1 diabetes worldwide 1990-1999. Diabet Med. 2006, 23 (8 ): 857-866. 10.1111/j.1464-5491.2006.01925.x.
The WHO Multinational Project for Childhood Diabetes Group: Familial insulin-dependent diabetes mellitus (IDDM) epidemiology: standardization of data for the DIAMOND Project. The WHO Multinational Project for Childhood Diabetes Group. Bull World Health Organ. 1991, 69 (6): 767-777.
Petrovsky N, Schatz DA: The immunology of human type 1 diabetes. Textbook of Diabetes 1. Edited by: Pickup JC, Williams G. 2003, London , Blackwell Science Ltd, 1: 18.1-18.14. 3rd
Pitkaniemi J, Onkamo P, Tuomilehto J, Arjas E: Increasing incidence of Type 1 diabetes--role for genes?. BMC Genet. 2004, 5: 5-10.1186/1471-2156-5-5.
Thomson G, Robinson WP, Kuhner MK, Joe S, MacDonald MJ, Gottschall JL, Barbosa J, Rich SS, Bertrams J, Baur MP, et al: Genetic heterogeneity, modes of inheritance, and risk estimates for a joint study of Caucasians with insulin-dependent diabetes mellitus. Am J Hum Genet. 1988, 43 (6): 799-816.
Harjutsalo V, Podar T, Tuomilehto J: Cumulative Incidence of Type 1 Diabetes in 10,168 Siblings of Finnish Young-Onset Type 1 Diabetic Patients. Diabetes. 2005, 54 (2): 563-569. 10.2337/diabetes.54.2.563.
Field LL: Genetic linkage and association studies of Type I diabetes: challenges and rewards. Diabetologia. 2002, 45 (1): 21-35. 10.1007/s125-002-8241-7.
Barnett AH, Eff C, Leslie RD, Pyke DA: Diabetes in identical twins. A study of 200 pairs. Diabetologia. 1981, 20 (2): 87-93. 10.1007/BF00262007.
Olmos P, A'Hern R, Heaton DA, Millward BA, Risley D, Pyke DA, Leslie RD: The significance of the concordance rate for type 1 (insulin-dependent) diabetes in identical twins. Diabetologia. 1988, 31 (10): 747-750. 10.1007/BF00274777.
Kaprio J, Tuomilehto J, Koskenvuo M, Romanov K, Reunanen A, Eriksson J, Stengard J, Kesaniemi YA: Concordance for type 1 (insulin-dependent) and type 2 (non-insulin-dependent) diabetes mellitus in a population-based cohort of twins in Finland. Diabetologia. 1992, 35 (11): 1060-1067. 10.1007/BF02221682.
Kumar D, Gemayel NS, Deapen D, Kapadia D, Yamashita PH, Lee M, Dwyer JH, Roy-Burman P, Bray GA, Mack TM: North-American twins with IDDM. Genetic, etiological, and clinical significance of disease concordance according to age, zygosity, and the interval after diagnosis in first twin. Diabetes. 1993, 42 (9): 1351-1363. 10.2337/diabetes.42.9.1351.
Kyvik KO, Green A, Beck-Nielsen H: Concordance rates of insulin dependent diabetes mellitus: a population based study of young Danish twins. BMJ. 1995, 311 (7010): 913-917.
Hyttinen V, Kaprio J, Kinnunen L, Koskenvuo M, Tuomilehto J: Genetic Liability of Type 1 Diabetes and the Onset Age Among 22,650 Young Finnish Twin Pairs: A Nationwide Follow-Up Study . Diabetes. 2003, 52 (4): 1052-1055. 10.2337/diabetes.52.4.1052.
Davies JL, Kawaguchi Y, Bennett ST, Copeman JB, Cordell HJ, Pritchard LE, Reed PW, Gough SC, Jenkins SC, Palmer SM, et al: A genome-wide search for human type 1 diabetes susceptibility genes. Nature. 1994, 371 (6493): 130-136. 10.1038/371130a0.
Hashimoto L, Habita C, Beressi JP, Delepine M, Besse C, Cambon-Thomsen A, Deschamps I, Rotter JI, Djoulah S, James MR, et al: Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome 11q. Nature. 1994, 371 (6493): 161-164. 10.1038/371161a0.
Mein CA, Esposito L, Dunn MG, Johnson GC, Timms AE, Goy JV, Smith AN, Sebag-Montefiore L, Merriman ME, Wilson AJ, Pritchard LE, Cucca F, Barnett AH, Bain SC, Todd JA: A search for type 1 diabetes susceptibility genes in families from the United Kingdom. Nat Genet. 1998, 19 (3): 297-300. 10.1038/991.
Concannon P, Gogolin-Ewens KJ, Hinds DA, Wapelhorst B, Morrison VA, Stirling B, Mitra M, Farmer J, Williams SR, Cox NJ, Bell GI, Risch N, Spielman RS: A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus. Nat Genet. 1998, 19 (3): 292-296. 10.1038/985.
Cox NJ, Wapelhorst B, Morrison VA, Johnson L, Pinchuk L, Spielman RS, Todd JA, Concannon P: Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families. Am J Hum Genet. 2001, 69 (4): 820-830. 10.1086/323501.
Nerup J, Pociot F: A genomewide scan for type 1-diabetes susceptibility in Scandinavian families: identification of new loci with evidence of interactions. Am J Hum Genet. 2001, 69 (6): 1301-1313. 10.1086/324341.
Bergholdt R, Nerup J, Pociot F: Fine mapping of a region on chromosome 21q21.11-q22.3 showing linkage to type 1 diabetes. J Med Genet. 2005, 42 (1): 17-25. 10.1136/jmg.2004.022004.
Concannon P, Erlich HA, Julier C, Morahan G, Nerup J, Pociot F, Todd JA, Rich SS: Type 1 diabetes: evidence for susceptibility loci from four genome-wide linkage scans in 1,435 multiplex families. Diabetes. 2005, 54 (10): 2995-3001. 10.2337/diabetes.54.10.2995.
Bennett ST, Lucassen AM, Gough SC, Powell EE, Undlien DE, Pritchard LE, Merriman ME, Kawaguchi Y, Dronsfield MJ, Pociot F, et al: Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus. Nat Genet. 1995, 9 (3): 284-292. 10.1038/ng0395-284.
Bain SC, Kelly MA, Mijovic CH, Barbett AH: Genetic factors in the pathogenesis of type 1 diabetes. Textbook of Diabetes 1. Edited by: Pickup JC, Williams G. 2003, London , Blackwell Science Ltd, 1: 15.1-15.13.
Todd JA, Walker NM, Cooper JD, Smyth DJ, Downes K, Plagnol V, Bailey R, Nejentsev S, Field SF, Payne F, Lowe CE, Szeszko JS, Hafler JP, Zeitels L, Yang JH, Vella A, Nutland S, Stevens HE, Schuilenburg H, Coleman G, Maisuria M, Meadows W, Smink LJ, Healy B, Burren OS, Lam AA, Ovington NR, Allen J, Adlem E, Leung HT, Wallace C, Howson JM, Guja C, Ionescu-Tìrgovişte C, Genetics of Type 1 Diabetes in Finland, Simmonds MJ, Heward JM, Gough SC, Wellcome Trust Case Control Consortium, Dunger DB, Wicker LS, Clayton DG: Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. Nat Genet. 2007, 39 (7): 857-864. 10.1038/ng2068.
Osterholm AM, He B, Pitkaniemi J, Albinsson L, Berg T, Sarti C, Tuomilehto J, Tryggvason K: Genome-wide scan for type 1 diabetic nephropathy in the Finnish population reveals suggestive linkage to a single locus on chromosome 3q. Kidney Int. 2006
Rogus JJ, Krolewski AS: Using discordant sib pairs to map loci for qualitative traits with high sibling recurrence risk. Am J Hum Genet. 1996, 59 (6): 1376-1381.
Gretarsdottir S, Sveinbjornsdottir S, Jonsson HH, Jakobsson F, Einarsdottir E, Agnarsson U, Shkolny D, Einarsson G, Gudjonsdottir HM, Valdimarsson EM, Einarsson OB, Thorgeirsson G, Hadzic R, Jonsdottir S, Reynisdottir ST, Bjarnadottir SM, Gudmundsdottir T, Gudlaugsdottir GJ, Gill R, Lindpaintner K, Sainz J, Hannesson HH, Sigurdsson GT, Frigge ML, Kong A, Gudnason V, Stefansson K, Gulcher JR: Localization of a susceptibility gene for common forms of stroke to 5q12. Am J Hum Genet. 2002, 70 (3): 593-603. 10.1086/339252.
Palsson B, Palsson F, Perlin M, Gudbjartsson H, Stefansson K, Gulcher J: Using quality measures to facilitate allele calling in high-throughput genotyping. Genome Res. 1999, 9 (10): 1002-1012. 10.1101/gr.9.10.1002.
Risch N: Linkage strategies for genetically complex traits. I. Multilocus models. Am J Hum Genet. 1990, 46 (2): 222-228.
Lander ES, Schork NJ: Genetic dissection of complex traits. Science. 1994, 265 (5181): 2037-2048. 10.1126/science.8091226.
Lander E, Kruglyak L: Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet. 1995, 11 (3): 241-247. 10.1038/ng1195-241.
Cordell HJ, Todd JA, Bennett ST, Kawaguchi Y, Farrall M: Two-locus maximum lod score analysis of a multifactorial trait: joint consideration of IDDM2 and IDDM4 with IDDM1 in type 1 diabetes. Am J Hum Genet. 1995, 57 (4): 920-934.
Cordell HJ, Wedig GC, Jacobs KB, Elston RC: Multilocus linkage tests based on affected relative pairs. Am J Hum Genet. 2000, 66 (4): 1273-1286. 10.1086/302847.
Holmans P: Asymptotic properties of affected-sib-pair linkage analysis. Am J Hum Genet. 1993, 52 (2): 362-374.
Kruglyak L, Lander ES: Complete multipoint sib-pair analysis of qualitative and quantitative traits. Am J Hum Genet. 1995, 57 (2): 439-454.
Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES: Parametric and nonparametric linkage analysis: a unified multipoint approach. Am J Hum Genet. 1996, 58 (6): 1347-1363.
Abecasis GR, Cherny SS, Cookson WO, Cardon LR: Merlin--rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet. 2002, 30 (1): 97-101. 10.1038/ng786.
Blackwelder WC, Elston RC: A comparison of sib-pair linkage tests for disease susceptibility loci. Genet Epidemiol. 1985, 2 (1): 85-97. 10.1002/gepi.1370020109.
This work has been supported by the grants from the Academy of Finland (46558, 51224, 51225, 118492), NIH, Novo Nordisk Foundation and Sigrid Juselius Foundation. We are grateful to Tuula Tenkula, Leena Ollitervo and Maire Jarva for technical assistance and Laura Haapala for data management. We also owe our sincere thanks to Inga Reynisdottir in the deCODE Genetics, Reykjavik, Iceland for kindly help in genotyping and editing the genotype data.
QQ participated in the data analysis and drafting of the manuscript; AMÖ and BH took part in the genotyping, managed and analyzed the data and approved the final version of the manuscript; JP and HJC participated in the data analysis and drafting of the manuscript; CS collected the data and approved the final version of the manuscript; LK collected the data and approved the final version of the manuscript; ETW participated in the concept and design of the study and approved the final version of the manuscript; KT and JT were responsible for the conception, funding, design and coordination of the study, approved the final version of the manuscript.
Qing Qiao, Anne-May Österholm, Bing He contributed equally to this work.
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Qiao, Q., Österholm, A., He, B. et al. A genome-wide scan for type 1 diabetes susceptibility genes in nuclear families with multiple affected siblings in Finland. BMC Genet 8, 84 (2007) doi:10.1186/1471-2156-8-84
- Diabetic Nephropathy
- Diabetes Susceptibility Gene
- Rare Mendelian Disease
- Sibling Relative Risk
- Marshfield Medical Research Foundation