- Research article
- Open Access
- Open Peer Review
Linkage study of fibrinogen levels: the Strong Heart Family Study
BMC Medical Genetics volume 9, Article number: 77 (2008)
The pathogenesis of atherosclerosis involves both hemostatic and inflammatory mechanisms. Fibrinogen is associated with both risk of thrombosis and inflammation. A recent meta-analysis showed that risk of coronary heart disease may increase 1.8 fold for 1 g/L of increased fibrinogen, independent of traditional risk factors. It is known that fibrinogen levels may be influenced by demographic, environmental and genetic factors. Epidemiologic and candidate gene studies are available; but few genome-wide linkage studies have been conducted, particularly in minority populations. The Strong Heart Study has demonstrated an increased incidence of cardiovascular disease in the American Indian population, and therefore represents an important source for genetic-epidemiological investigations.
The Strong Heart Family Study enrolled over 3,600 American Indian participants in large, multi-generational families, ascertained from an ongoing population-based study in the same communities. Fibrinogen was determined using standard technique in a central laboratory and extensive additional phenotypic measures were obtained. Participants were genotyped for 382 short tandem repeat markers distributed throughout the genome; and results were analyzed using a variance decomposition method, as implemented in the SOLAR 2.0 program.
Data from 3535 participants were included and after step-wise, linear regression analysis, two models were selected for investigation. Basic demographic adjustments constituted model 1, while model 2 considered waist circumference, diabetes mellitus and postmenopausal status as additional covariates. Five LOD scores between 1.82 and 3.02 were identified, with the maximally adjusted model showing the highest score on chromosome 7 at 28 cM. Genes for two key components of the inflammatory response, i.e. interleukin-6 and "signal transducer and activator of transcription 3" (STAT3), were identified within 2 and 8 Mb of this 1 LOD drop interval respectively. A LOD score of 1.82 on chromosome 17 between 68 and 93 cM is supported by reports from two other populations with LOD scores of 1.4 and 1.95.
In a minority population with a high prevalence of cardiovascular disease, strong evidence for a novel genetic determinant of fibrinogen levels is found on chromosome 7 at 28 cM. Four other loci, some of which have been suggested by previous studies, were also identified.
Hypotheses concerning the pathogenesis of atherosclerosis have frequently included both hemostatic and inflammatory mechanisms. Fibrinogen levels are positively associated with risk of thrombosis  and are also an indicator of acute inflammatory response [2, 3]. A recent, large meta-analysis  concluded that for each 1 g/L increase in plasma fibrinogen, individuals increase their relative risk of coronary heart disease (CHD) by 1.8 after adjustment for major cardiovascular disease (CVD) risk factors. The Strong Heart Study (SHS) is an ongoing, longitudinal cohort study of CVD among American Indians in three regions of the US, and began in 1988. The current report is derived from the Strong Heart Family Study (SHFS), an extension of the SHS, in which we have previously corroborated the ability of fibrinogen to predict CVD events . The above studies have identified fibrinogen as a predictor of CVD independent of other standard risk factors [6, 7], however it is possible that fibrinogen levels are simply correlated with other causal inflammatory factors .
Fibrinogen levels are increased by many non-genetic factors, e.g. advancing age, smoking, obesity, oral contraceptive use and estrogen replacement therapy, whereas moderate alcohol intake has been related to lower fibrinogen levels [7, 9, 10]. Acquired metabolic conditions, e.g. obesity, insulin resistance and type 2 diabetes also increase fibrinogen levels [7, 11]. Correlation between fibrinogen and other hemostatic/inflammatory markers has been demonstrated [12, 13].
Moderate heritabilities of 34% and 37% were found in two primarily Caucasian populations [9, 14]. In our previous work, we demonstrated a heritability between 33 ± 6% and 44 ± 6% among the American Indian participants of the SHFS . Genome-wide linkage studies of fibrinogen [16–18] are uncommon; but have identified a number of suggestive quantitative trait loci (QTL). Polymorphisms of the fibrinogen gene have been extensively investigated for their influence on circulating protein levels [19–24].
Cardiovascular disease accounts for a large proportion of mortality and morbidity in American Indian (AI) communities . Since a substantial number of individuals with CVD events have no previously identifiable risk factors , it is important to develop the means to more accurately predict CVD events. Although fibrinogen has been shown to provide risk information independent of HDL, total cholesterol and other typical cardiovascular risk factors [4, 6]; a better understanding of the genetic and environmental factors that influence variation in circulating fibrinogen levels may improve our understanding of CVD.
The Strong Heart Study (SHS) is a population-based, cohort study of cardiovascular disease among American Indians. The participating communities, study design, survey methods and laboratory techniques have been described previously [26, 27]. In 1998, the Strong Heart Family Study, was initiated and participants 16 years and older were recruited, without regard to disease status, from multi-generational families, including index members of the SHS cohort. All participants have given informed consent for the genetic study of CVD and associated risk factors, including the present study. In addition, approval for this study was obtained from relevant tribal communities and institutional review boards.
The protocols for collection of all phenotypic data were briefly described in previous publications . Fibrinogen was measured with a coefficient of variation (CV) of < 8%, using the Clauss method  incorporating STA Fibrinogen-5 reagents on the STA-R platform, both from Diagnostica Stago. "Ever" smoking was defined as having smoked at least 100 cigarettes during the lifetime and "current" smoking (present, regular use of smoke tobacco). "Current" and "ever" consumption of alcohol was defined as having had at least 12 alcoholic beverages in the last year or in past years, respectively.
The procedures for genotyping in the SHFS have been described previously . In brief, DNA was isolated from fasting blood samples using organic solvents, and then amplified in separate PCR reactions with primers specific for short tandem repeat markers using the ABI PRISM Linkage Mapping Set-MD10 Version 2.5 (Applied Biosystems, Foster City, CA). PCR products were loaded into an ABI PRISM 377 DNA sequencer for laser-based automated genotyping. Analyses and assignment of the marker alleles were done using computerized algorithms (Applied Biosystems). deCODE Genetics provided sex-averaged chromosomal maps (in units of Haldane centimorgans) for this analysis. Pedigrees were screened with the PREST (Pedigree Relationship Statistical Tests)  and Sim Walk2  programs for mendelian inconsistencies and possible double recombinants. The above screening resulted in less than 1% of all genotypes being excluded.
SAS, version 8.0, was used to screen covariates for statistical significance using stepwise linear regression by center. Univariate quantitative genetic analyses were used to partition the phenotypic variance into its' additive genetic and environmental components, using maximum likelihood variance decomposition methods . This approach was implemented in the computer program SOLAR, version 2.0  and allows for an explicit test of whether correlations among family members are in part due to genetic effects.
The use of the variance component approach requires an estimate of the identity-by-descent (IBD) matrix. We used the Loki package , which employs a Markov chain Monte Carlo stochastic procedure to compute the IBD allele sharing at points throughout the genome conditional on the genotype information available at neighboring points.
A total of 3535 SHFS participants were considered for analysis (Arizona (AZ) = 1195, Dakota (DA) = 1158, Oklahoma (OK) = 1182) after excluding those individuals with missing covariate data and as indicated below to normalize the phenotypic trait distribution. Because variance components methods are sensitive to kurtosis , all phenotypic outliers (here defined as any value more than 3 standard deviations from the mean) were removed prior to analysis (number excluded varies by analysis, N < 15). In addition, fibrinogen levels were natural log transformed. All analyses were conducted separately for each center and then on the combined data from all three centers. To maximize our power to detect genetic effects, a minimally adjusted model (Model 1), incorporating age, sex, age by sex and center covariates was analyzed first. Secondary analyses considered adjustment for the linear fixed effects of the covariates listed in Table 1, all of which were identified from the published literature. Covariates whose effects were significant (P < 0.05) in the initial analysis in at least one Center were retained in the maximally adjusted model of all Centers (Model 2), even if the significance levels decreased after inclusion of other covariates. This process resulted in the addition of waist circumference, the presence of ADA defined diabetes  and postmenopausal status to Model 2. The addition of current smoking as a covariate resulted in variable and insignificant changes to the outcome, compared with Model 2. We additionally confirmed the significance of Model 2 covariates while accounting for family relationships in SOLAR. Residuals were generated for both models (Model 1 and Model 2) and used in all subsequent genetic analyses. Kurtosis values for fibrinogen were < 0.50 for all analyses.
The power of this study for each center was estimated by simulations, assuming fully informative markers. The simulations were based on a total heritability of the fibrinogen phenotype either 25% or 50%. An estimate of the power for all centers combined was determined by calculations based on the results from the individual centers, due to the otherwise extremely high computational demands for simulations.
The statistical descriptors of fibrinogen and other covariates are stratified by center and displayed in table 1. The unadjusted fibrinogen levels were highest (417.5 mg/dl ± 87) in the Arizona center and the lowest (366.7 mg/dl ± 80) in the Dakota center. Individuals from the Arizona Center had the highest prevalence of diabetes and obesity. In contrast, SHFS participants from the Dakotas Center had the highest prevalence of current smokers. The highest prevalence of menopause was in the Oklahoma Center, perhaps since they were older on average.
Table 2 presents all suggestive (LOD ≥ 1.8)  genome-wide, multipoint linkage scores of fibrinogen by center and model. A QTL for fibrinogen (LOD = 3.02) was detected in the Dakota Center on chromosome 7 at 28 centimorgans. The 1-cM LOD unit support interval spanned 18 cM, from 17 to 35 cM (9,706,961 to 21,871,858 Mb P terminus).
Further suggestive evidence of linkage to fibrinogen was observed in the Oklahoma center on chromosome 3 at 166 cM. The 1-cM LOD unit support interval spanned 15 centimorgans from 157 – 172 cM (144,754,119 to 164,001,645 Mb). In addition, we found suggestive evidence of linkage to fibrinogen within all centers combined to chromosome 6 at 122 cM. Of the suggestive LOD scores, the only one that declined with adjustment was at chromosome 6, 122 centimorgans, in the analysis including all centers. In a post-hoc analysis, the only available measure of inflammatory state, white blood cell count (WBC), was included with previously described models to adjust for inflammatory state. LOD scores in these analyses showed essentially identical values for OK, model 2, and DK, chromosome 7, model 1 of 2.51 and 2.81 respectively. The LOD score for DK, chromosome 7, model 2 was reduced slightly to 2.41 and became insignificant (0.51) for DK, chromosome 17, model 2.
While the α,β,γ fibrinogen genes are on chromosome 4, the present study shows LOD scores for the DK center only at 4q28, 155cM, ranging between 1.36 for Model 2 to 1.70 for Model 1; none of the other centers exhibited LOD scores over 0.3 in this region.
Assuming a genome-wide heritability of 25%, power calculations indicated an 80% power to detect a locus with a LOD score > 3 for a locus contributing a minimum of between 15 and 20% of total variance for each of the three centers and 10% for all centers combined.
Evidence for a pathophysiologic role of both thrombotic and inflammatory influences on atherosclerosis continues to accumulate. The fact that fibrinogen was shown in 31 prospective studies involving over 150,000 participants (without apparent disease at baseline) to predict future CVD events is compelling, but not absolute, support for a primary role in the development of atherosclerosis.  The influence of fibrinogen would appear to be enhanced among those with a high prevalence of diabetes, smoking and other environmental influences , including the presently described SHS population .
In addition to multiple environmental influences on plasma fibrinogen levels [7, 9] the effects of heritability [9, 14, 15] and specific genetic variants (primarily involving the 3 fibrinogen gene cluster) are well established [19–24, 37]
While genetic polymorphisms in the fibrinogen genes are found in diverse populations around the world [38, 39], and a role for variants of the α,β,γ fibrinogen genes has been reported , there still appears to be substantial variation due to unknown genetic effects . Although the Dakota center found modest genetic effects at the fibrinogen gene cluster on chromosome 4 (LOD 1.7), this was not seen at either of the other two centers. Other investigators have failed to demonstrate linkage to the fibrinogen gene loci in otherwise adequately powered studies [18, 41]., It would be of interest to determine if the common polymorphisms (such as the -455G/A variant of the β gene promoter) seen in other populations  at this locus are simply not well represented in these centers, or whether they lack the typical effect size.
Suggestive evidence of linkage to novel loci was identified in this study on chromosomes 3 (OK center), 6 (all centers combined) and both 7 and 17 (DK center). Our linkage results at 3q22.2 (166 cM, closest to marker D3S1299) are within 0.5 Mb of the angiotensin II receptor, type 1 gene (AGTR1, 149.4 Mb-150.1 Mb) and this gene is thus well within the 1 LOD interval (144.8 Mb-169.8 Mb). The angiotensin converting enzyme I (ACE1) gene is also located within the 1 LOD interval of our suggestive locus at chromosome 17 (68 cM to 93 cM)  Although AGTR1, ACE1, and fibrinogen all have relevance to CVD, there is no readily apparent physiologic connection between fibrinogen levels and the renin-angiotensin-system (RAS). While the RAS is an important factor in the regulation of blood pressure, and fibrinogen is often elevated in the presence of hypertension, we are unaware of any evidence that increased fibrinogen preceeds or influences the development of hypertension. It is possible that a genetic variant in this locus simultaneously controlling expression of both fibrinogen and RAS genes.
Findings of Ding et al  support our results at 6q21, see Table 3. There are 143 genes within the 1 LOD confidence limits of the locus at 6q21 (122 cM, closest to marker D6S303); but none have obvious relationships with fibrinogen.
Within the 1 LOD drop interval at 7p21.1 (28 cM, closest to marker D7S507), the integrin beta-8 (ITGB8) gene is located at 31 cM. This gene is related to ITGB3 (see below) and shares similar important relationships with transforming growth factor, beta 1 (TGFB1) and other elements of the immune system [43, 44]. The interleukin-6 gene (IL6) is located 2 Mb beyond the 1 LOD drop interval on 7p21 at 22.7 Mb, closest to deCODE markers at 41.69 cM. Zhang et al  have shown a correlation between IL6 and fibrinogen levels (r = 0.22, p < 0.0001). Not all , but some IL6 polymorphisms are known to affect fibrinogen levels . The central role of IL6 in inflammatory physiology would make this a strong candidate for effects on fibrinogen as an acute phase reactant, although the fact that the DK LOD score at this locus was essentially unchanged with adjustment for an inflammatory marker (WBC) suggests inflammatory stimuli are not the sole determinants of fibrinogen levels.
Our findings at chromosome 17, 76 cM (nearest marker D17S1607) are in close proximity to the LOD of 1.4 found by Yang et al  at 96 cM (on the Marshfield map). The growth hormone (GH1) lies within the 1 LOD drop interval and exerts an influence on fibrinogen levels . The integrin, beta-3 (ITGB3) and "signal transducer and activator of transcription 3" (STAT3) genes both reside within 3 and 8 Mb respectively of this 17q23.3 interval and both are known to affect baseline and acute phase fibrinogen expression [41, 49].
These current findings derive from specific subsets of the North American Indian population and each center of the study analyzes a group essentially the same size as that reported from the Framingham Heart Study . One might expect more homogeneous findings among these American Indian populations; but they are separated by about 1,000 Km and have distinct language and cultural characteristics. The SHS has found similar diversity between centers in the analysis of other phenotypes. The lack of apparent effect in the AZ and OK centers of the fibrinogen gene cluster at chromosome 4q28, in comparison to Caucasian populations, further highlights apparent differences between ethnic groups. No overlapping linkage regions with LOD scores over 1.3 were found in comparing African Americans and non-Hispanic whites in the GENOA study , although limitations of power may have been a factor. The relative lack of consistency in linkage study findings has been commented on before and our findings are consistent with this . Perhaps unappreciated environmental effects are present, which have not been fully accounted for in the adjustment strategies used by various investigators.
Strengths of this study include the population-based recruitment with large numbers of participants analyzed and the large, multi-generational families recruited. Our calculations indicate an 80% power to identify a QTL with a LOD score of more than 3 contributing at least 20% of the total phenotypic variance in any center. In spite of the above-mentioned diversity of findings, the genetic background of the populations are likely to be more uniform than population-based studies from urban areas. The prospective collection of a very well characterized phenotype, including many demographic, environmental and physiologic parameters is another strength.
Although the large size of the families in this study increases the power to detect genetic effects, it may also magnify the effects of uncommon polymorphisms in a particular family. This should be minimized by the fact that recruitment for the family study was not based on the presence or history of CVD and the fact that 13.6% of the family study participants were also members of the original, population-based cohort.
In a minority population with a high prevalence of cardiovascular disease, strong evidence for a novel genetic determinant of fibrinogen levels is found on chromosome 7 at 28 cM. Four other loci, some of which have been suggested by previous studies, were also identified. Fibrinogen is of particular interest since it may act through two independent pathophysiologic mechanisms, i.e. thrombosis and inflammation. A better understanding of the genetic determinants of fibrinogen levels and how they influence the development of atherosclerosis and its complications will assist in fashioning better preventive and treatment strategies for this very serious public health problem.
Di Minno G, Cerbone A, Margaglione M, Vecchione G, Grandone E, Mancini M: Fibrinogen and mechanisms of thrombosis. A difficult link. Eur J Epidemiol. 1992, 8 Suppl 1: 88-91.
Mahmoudi M, Curzen N, Gallagher PJ: Atherogenesis: the role of inflammation and infection. Histopathology. 2007, 50: 535-46.
Tracy RP: Inflammation markers and coronary heart disease. Curr Opin Lipidol. 1999, 10: 435-41.
Fibrinogen Studies Collaboration, Danesh J, Lewington S, Thompson SG, Lowe GD, Collins R, Kostis JB, Wilson AC, Folsom AR, Wu K, Benderly M, Goldbourt U, Willeit J, Kiechl S, Yarnell JW, Sweetnam PM, Elwood PC, Cushman M, Psaty BM, Tracy RP, Tybjaerg-Hansen A, Haverkate F, de Maat MP, Fowkes FG, Lee AJ, Smith FB, Salomaa V, Harald K, Rasi R, Vahtera E, Jousilahti P, Pekkanen J, D'Agostino R, Kannel WB, Wilson PW, Tofler G, Arocha-Piñango CL, Rodriguez-Larralde A, Nagy E, Mijares M, Espinosa R, Rodriquez-Roa E, Ryder E, Diez-Ewald MP, Campos G, Fernandez V, Torres E, Marchioli R, Valagussa F, Rosengren A, Wilhelmsen L, Lappas G, Eriksson H, Cremer P, Nagel D, Curb JD, Rodriguez B, Yano K, Salonen JT, Nyyssönen K, Tuomainen TP, Hedblad B, Lind P, Loewel H, Koenig W, Meade TW, Cooper JA, De Stavola B, Knottenbelt C, Miller GJ, Cooper JA, Bauer KA, Rosenberg RD, Sato S, Kitamura A, Naito Y, Palosuo T, Ducimetiere P, Amouyel P, Arveiler D, Evans Ae, Ferrieres J, Juhan-Vague I, Bingham A, Schulte H, Assmann G, Cantin B, Lamarche B, Després JP, Dagenais GR, Tunstall-Pedoe H, Woodward M, Ben-Shlomo Y, Davey Smith G, Palmieri V, Yeh JL, Rudnicka A, Ridker P, Rodeghiero F, Tosetto A, Shepherd J, Ford I, Robertson M, Brunner E, Shipley M, Feskens EJ, Kromhout D, Dickinson A, Ireland B, Juzwishin K, Kaptoge S, Lewington S, Memon A, Sarwar N, Walker M, Wheeler J, White I, Wood A: Plasma fibrinogen level and the risk of major cardiovascular diseases andnonvascular mortality: an individual participant meta-analysis. JAMA. 2005, 294: 1799-809.
Palmieri V, Celentano A, Roman MJ, de Simone G, Best L, Lewis MR, Robbins DC, Fabsitz RR, Howard BV, Devereux RB: Relation of fibrinogen to cardiovascular events is independent of preclinical cardiovascular disease: the Strong Heart Study. Am Heart J. 2003, 145: 467-74.
Ridker PM: Novel risk factors and markers for coronary disease. Adv Intern Med. 2000, 45: 391-418.
Juhan-Vague I: Haemostatic parameters and vascular risk. Atherosclerosis. 1996, 124 (Suppl): S49-S55.
Packard CJ, O'Reilly DS, Caslake MJ, McMahon AD, Ford I, Cooney J, Macphee CH, Suckling KE, Krishna M, Wilkinson FE, Rumley A, Lowe GD: Lipoprotein-associated phospholipase A2 as an independent predictor of coronary heart disease. West of Scotland Coronary Prevention Study Group. N Engl J Med. 2000, 343: 1148-55.
Pankow JS, Folsom AR, Province MA, Rao DC, Williams RR, Eckfeldt J, Sellers TA: Segregation analysis of plasminogen activator inhibitor-1 and fibrinogen levels in the NHLBI family heart study. Arterioscler Thromb Vasc Biol. 1998, 18: 1559-67.
Johnson JV, Lowell J, Badger GJ, Rosing J, Tchaikovski S, Cushman M: Effects of oral and transdermal hormonal contraception on vascular risk markers: a randomized controlled trial. Obstet Gynecol. 2008, 111: 278-84.
Ford ES: The metabolic syndrome and C-reactive protein, fibrinogen, and leukocyte count:findings from the Third National Health and Nutrition Examination Survey. Atherosclerosis. 2003, 168: 351-8.
Haverkate F, Thompson SG, Duckert F: Haemostasis factors in angina pectoris; relation to gender, age and acute-phase reaction. Results of the ECAT Angina Pectoris Study Group. Thromb Haemost. 1995, 73: 561-7.
Haffner SM: Insulin resistance, inflammation, and the prediabetic state. Am J Cardiol. 2003, 92 (4A): 18J-26J.
Freeman MS, Mansfield MW, Barrett JH, Grant PJ: Genetic contribution to circulating levels of hemostatic factors in healthy families with effects of known genetic polymorphisms on heritability. Arterioscler Thromb Vasc Biol. 2002, 22: 506-10.
Best LG, North KE, Tracy RP, Lee ET, Howard BV, Palmieri V, Maccluer JW: Genetic determination of acute phase reactant levels: the strong heart study. Hum Hered. 2004, 58: 112-6.
Yang Q, Tofler GH, Cupples LA, Larson MG, Feng D, Lindpaintner K, Levy D, D'Agostino RB, O'Donnell CJ: A genome-wide search for genes affecting circulating fibrinogen levels in the Framingham Heart Study. Thromb Res. 2003, 110: 57-64.
Friedlander Y, Kark JD, Sinnreich R, Basso F, Humphries SE: Combined segregation and linkage analysis of fibrinogen variability in Israeli families: evidence for two quantitative-trait loci, one of which is linked to a functional variant (-58G > A) in the promoter of the alpha-fibrinogen gene. Ann Hum Genet. 2003, 67: 228-41.
Soria JM, Almasy L, Souto JC, Buil A, Lathrop M, Blangero J, Fontcuberta J: A genome search for genetic determinants that influence plasma fibrinogen levels. Arterioscler Thromb Vasc Biol. 2005, 25: 1287-92.
Ando R, Doi M, Yamauchi K, Chida Y, Ida T, Endo K, Yanagi H, Tomura S: Association of beta-fibrinogen and factor VII polymorphism with plasma fibrinogen and factor VII levels, and no association of PAI-1 polymorphism with plasma PAI-1 levels in hemodialysis patients. Clin Nephrol. 2002, 58: 25-32.
de Maat MP, Bladbjerg EM, Johansen LG, de Knijff P, Gram J, Kluft C, Jespersen J: DNA-polymorphisms and plasma levels of vascular disease risk factors in Greenland Inuit – is there a relation with the low risk of cardiovascular disease in the Inuit?. Thromb Haemost. 1999, 81: 547-52.
Cook DG, Cappuccio FP, Atkinson RW, Wicks PD, Chitolie A, Nakandakare ER, Sagnella GA, Humphries SE: Ethnic differences in fibrinogen levels: the role of environmental factors and the beta-fibrinogen gene. Am J Epidemiol. 2001, 153: 799-806.
de Maat MP, Kastelein JJ, Jukema JW, Zwinderman AH, Jansen H, Groenemeier B, Bruschke AV, Kluft C: -455G/A polymorphism of the beta-fibrinogen gene is associated with the progression of coronary atherosclerosis in symptomatic men: proposed role for an acute-phase reaction pattern of fibrinogen. REGRESS group. Arterioscler Thromb Vasc Biol. 1998, 18: 265-71.
Brull DJ, Dhamrait S, Moulding R, Rumley A, Lowe GD, World MJ, Humphries SE, Montgomery HE: The effect of fibrinogen genotype on fibrinogen levels after strenuous physical exercise. Thromb Haemost. 2002, 87: 37-41.
Margaglione M, Bossone A, Cappucci G, Colaizzo D, Grandone E, Di Minno G: The effect of the interleukin-6 c/g-174 polymorphism and circulating interleukin-6 on fibrinogen plasma levels. Haematologica. 2001, 86: 199-204.
Howard BV, Lee ET, Cowan LD, Devereux RB, Galloway JM, Go OT, Howard WJ, Rhoades ER, Robbins DC, Sievers ML, Welty TK: Rising tide of cardiovascular disease in American Indians. The Strong Heart Study. Circulation. 1999, 99: 2389-2395.
Lee ET, Welty TK, Fabsitz R, Cowan LD, Le NA, Oopik AJ, Cucchiara AJ, Savage PJ, Howard BV: The Strong Heart Study. A study of cardiovascular disease in American Indians: design and methods. Am J Epidemiol. 1990, 132: 1141-55.
North KE, Howard BV, Welty TK, Best LG, Lee ET, Yeh JL, Fabsitz RR, Roman MJ, MacCluer JW: Genetic and environmental contributions to cardiovascular disease risk in American Indians: the strong heart family study. Am J Epidemiol. 2003, 157: 303-14.
Clauss A: Rapid physiological coagulation method for the determination of fibrinogen. Acta Hematol. 1957, 17: 237-46.
North KE, Göring HH, Cole SA, Diego VP, Almasy L, Laston S, Cantu T, Howard BV, Lee ET, Best LG, Fabsitz RR, MacCluer JW: Linkage analysis of LDL cholesterol in American Indian populations: the Strong Heart Family Study. J Lipid Res. 2006, 47: 59-66.
Sun L, Wilder K, McPeek MS: Enhanced pedigree error detection. Hum Hered. 2002, 54: 99-110.
Sobel E, Papp JC, Lange K: Detection and integration of genotyping errors in statistical genetics. Am J Hum Genet. 2002, 70: 496-508.
Almasy L, Blangero J: Multipoint quantitative-trait linkage analysis in general pedigrees. Am J Hum Genet. 1998, 62: 1198-211.
Heath SC: Markov chain Monte Carlo segregation and linkage analysis for oligogenic models. Am J Hum Genet. 1997, 61: 748-60.
Blangero J, Williams JT, Almasy L: Quantitative trait locus mapping using human pedigrees. Hum Biol. 2000, 72: 35-62.
Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Diabetes care. 1997, 20: 1183-1197.
Rao DC, Gu C: False positives and false negatives in genome scans. Adv Genet. 2001, 42: 487-98.
Kathiresan S, Yang Q, Larson MG, Camargo AL, Tofler GH, Hirschhorn JN, Gabriel SB, O'Donnell CJ: Common genetic variation in five thrombosis genes and relations to plasma hemostatic protein level and cardiovascular disease risk. Arterioscler Thromb Vasc Biol. 2006, 26: 1405-12.
Liu Y, Saha N, Heng CK, Hong S, Low PS: Fibrinogen genotypes (alpha and beta) are associated with plasma fibrinogen levels in Chinese. J Med Genet. 2001, 38: E31-
Mannila MN, Silveira A, Hawe E, Eriksson P, Aillaud MF, Juhan-Vague I, Yudkin J, Margaglione M, di Minno G, Mussoni L, Tremoli E, Humphries S, Hamsten A: Plasma fibrinogen concentration predicts the risk of myocardial infarction differently in various parts of Europe: effects of beta-fibrinogen genotype and environmental factors. The HIFMECH Study. Thromb Haemost. 2004, 92: 1240-9.
Reiner AP, Carty CL, Carlson CS, Wan JY, Rieder MJ, Smith JD, Rice K, Fornage M, Jaquish CE, Williams OD, Tracy RP, Lewis CE, Siscovick DS, Boerwinkle E, Nickerson DA: Association between patterns of nucleotide variation across the three fibrinogen genes and plasma fibrinogen levels: the Coronary Artery Risk Development in Young Adults (CARDIA) study. J Thromb Haemost. 2006, 4: 1279-87.
Ding K, Feng D, de Andrade M, Mosley TH, Turner ST, Boerwinkle E, Kullo IJ: Genomic regions that influence plasma levels of inflammatory markers in hypertensive sibships. J Hum Hypertens. 2008, 22: 102-10.
Zhu X, Bouzekri N, Southam L, Cooper RS, Adeyemo A, McKenzie CA, Luke A, Chen G, Elston RC, Ward R: Linkage and association analysis of angiotensin I-converting enzyme (ACE)-gene polymorphisms with ACE concentration and blood pressure. Am J Hum Genet. 2001, 68: 1139-48.
Travis MA, Reizis B, Melton AC, Masteller E, Tang Q, Proctor JM, Wang Y, Bernstein X, Huang X, Reichardt LF, Bluestone JA, Sheppard D: Loss of integrin alpha(v)beta8 on dendritic cells causes autoimmunity and colitis in mice. Nature. 2007, 449: 361-5.
Wahl SM: Transforming growth factor-beta: innately bipolar. Curr Opin Immunol. 2007, 19: 55-62.
Zhang YY, Gottardo L, Mlynarski W, Frazier W, Nolan D, Duffy J, Marescotti MC, Gervino EV, Johnstone MT, Mantzoros CS, Avogaro A, Doria A: Genetic variability at the leptin receptor (LEPR) locus is a determinant of plasma fibrinogen and C-reactive protein levels. Atherosclerosis. 2007, 191: 121-7.
Wong LY, Leung RY, Ong KL, Cheung BM: Plasma levels of fibrinogen and C-reactive protein are related to interleukin-6 gene -572C>G polymorphism in subjects with and without hypertension. J Hum Hypertens. 2007, 21: 875-82.
Yang Q, Kathiresan S, Lin JP, Tofler GH, O'Donnell CJ: Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. BMC Med Genet. 2007, 8 (Suppl 1): S12-
Ahn CW, Kim CS, Nam JH, Kim HJ, Nam JS, Park JS, Kang ES, Cha BS, Lim SK, Kim KR, Lee HC, Huh KB: Effects of growth hormone on insulin resistance and atherosclerotic risk factors in obese type 2 diabetic patients with poor glycaemic control. Clin Endocrinol (Oxf). 2006, 64: 444-9.
Hou T, Ray S, Brasier AR: The functional role of an interleukin 6-inducible CDK9.STAT3 complex in human gamma-fibrinogen gene expression. J Biol Chem. 2007, 282: 37091-102.
Kruglyak L: The road to genome-wide association studies. Nat Rev Genet. 2008, 9: 314-8.
Yang Q, Tofler GH, Cupples LA, Larson MG, Feng D, Lindpaintner K, Levy D, D'Agostino RB, O'Donnell CJ: A genome-wide search for genes affecting circulating fibrinogen levels in the Framingham Heart Study. Thromb Res. 2003, 110: 57-64.
The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-2350/9/77/prepub
This work was supported by cooperative agreement grants U01-HL65520, U01-HL41642, U01-HL41652, U01-HL41654, and U01-HL65521 from the National Heart, Lung and Blood Institute, Bethesda, MD. We thank the SHS participants, Indian Health Service facilities, and participating tribal communities for their extraordinary cooperation and involvement, which has contributed to the success of the Strong Heart Study. A special thanks to Dick Howard, information technology assistant at University of North Carolina for his invaluable assistance in establishing the web-based access to the university computing node. The views expressed in this paper are those of the authors and do not necessarily reflect those of the Indian Health Service.
The authors declare that they have no competing interests.
All authors have read and approved the final manuscript. LGB: Originated and conducted the majority of the analysis, drafted the manuscript and is the corresponding author. KEN: Provided key oversight and direction of analysis and played a major role in editing the manuscript. XL: Provided initial linear regression analyses, residual files for linkage analysis and editing suggestions. VP: Offered important editorial suggestions for the manuscript. JGU: Supervised laboratory determinations of fibrinogen and made edits to the methods section. JM: Supervised genetic data collection and preparation. SL: Evaluated pedigrees, provided the final pedigree structure and performed the genotypic data cleaning. KH: Provided extensive quality control and data management of the genotyping. HG: Evaluated pedigrees and provided the final pedigree structure VPD: Provided "identical by descent" genotype files for analysis. Evaluated pedigrees and provided the final pedigree structure. LA: Guidance related to statistical linkage analysis. ETL: Phenotypic data collection and quality assurance. RPT: Guidance related to laboratory methodology. SC: Supervised the genotyping and provided important editorial comments.
About this article
Cite this article
Best, L.G., North, K.E., Li, X. et al. Linkage study of fibrinogen levels: the Strong Heart Family Study. BMC Med Genet 9, 77 (2008) doi:10.1186/1471-2350-9-77
- Quantitative Trait Locus
- Fibrinogen Level
- Short Tandem Repeat Marker
- Suggestive Quantitative Trait Locus