Skip to main content Accessibility help


  • Access
  • Cited by 20


      • Send article to Kindle

        To send this article to your Kindle, first ensure is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about sending to your Kindle. Find out more about sending to your Kindle.

        Note you can select to send to either the or variations. ‘’ emails are free but can only be sent to your device when it is connected to wi-fi. ‘’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

        Find out more about the Kindle Personal Document Service.

        Genetic studies of bipolar affective disorder in large families
        Available formats

        Send article to Dropbox

        To send this article to your Dropbox account, please select one or more formats and confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your <service> account. Find out more about sending content to Dropbox.

        Genetic studies of bipolar affective disorder in large families
        Available formats

        Send article to Google Drive

        To send this article to your Google Drive account, please select one or more formats and confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your <service> account. Find out more about sending content to Google Drive.

        Genetic studies of bipolar affective disorder in large families
        Available formats
Export citation



Genetic factors are known to be important in the aetiology of bipolar disorder.


To review linkage studies in extended families multiply affected with bipolar disorder.


Selective review of linkage studies of bipolar disorder emphasising the gains and drawbacks of studying large multiply-affected families and comparing the statistical methods used for data analysis.


Linkage of bipolar disorder to several chromosome regions including 4p, 4q, 10p, 12q, 16p, 18q, 21q and Xq has first been reported in extended families. In other families chromosomal rearrangements associated with affective illnesses provide signposts to the location of disease-related genes. Statistical analyses using variance component methods can be applied to extended families, require no prior knowledge of the disease inheritance, and can test multilocus models.


Studying single large pedigrees combined with variance component analysis is an efficient and effective strategy likely to lead to further insights into the genetic basis of bipolar disorders.


Declaration of interest

This work was supported by a grant from the Chief Scientist's Office, Scottish Executive.


Linkage analysis has been highly effective when used to identify the genes responsible for monogenic disorders, such as cystic fibrosis and Huntington's disease, but has been less consistent when applied to genetically complex conditions such as bipolar disorder, which are likely to be influenced by multiple genetic loci and by non-genetic environmental effects (Risch & Botstein, 1996). The lack of consistent findings from genome-wide linkage studies in bipolar disorder may be due to non-significant effects being reported or because different genes and/or different alleles at these genes are causing illness in different families and populations. Indeed, the hypothesis that different relatively uncommon alleles are segregating in different families would predict a lack of consistent findings across linkage studies based on sibling pairs or small families, since the power of the linkage approach is greatly reduced for diseases that show genetic heterogeneity (Terwilliger & Weiss, 1998). Bipolar disorder is likely to be genetically heterogeneous; mutations in one of several independent genes may produce a similar clinical phenotype and different mutations in the same gene may cause a variety of related symptoms. Another possible model is that the clinical symptoms of the affective disorders can be viewed as continuous variables, called quantitative traits, that are produced by the additive or interactive effects of mutations in two or more genes. Under this model, each gene — termed a quantitative trait locus (QTL) — has only a small effect on the trait, and symptoms develop as a result of the cumulative effects of mutations in several genes, probably combined with other internal and external environmental risk factors. In these situations there is also an advantage in studying single large pedigrees where the disease is likely to be caused by a more limited number of interacting genes and environmental factors.

The study of multiply-affected families with sufficient power on their own to generate significant evidence for linkage remains one of the most promising strategies to find genes implicated in bipolar disorder and other psychiatric conditions that may be characterised by extreme allelic complexity. Several chromosomal regions have been initially identified by linkage analysis in single families. These include chromosome 4p, reported in three studies of four extended pedigrees (Blackwood et al, 1996; Asherson et al, 1998; Ewald et al, 1998a ); chromosome 4q (Adams et al, 1998); chromosome 10p (Armstrong et al, 1997); chromosome 12q, where bipolar disorder, initially found to associate with Darier's disease (Craddock et al, 1994), was found to show linkage in large pedigrees studied independently (Barden et al, 1996; Ewald et al, 1998b ; Morissette et al, 1999); chromosome 16p (Ewald et al, 1995); chromosome 18q (Freimer et al, 1996); chromosome 21q (Straub et al, 1994); and chromosome Xq (Pekkarinen et al, 1995). The Old Order Amish, one of the largest extended families studied so far, has yielded several regions of suggestive linkage (Ginns et al, 1996; LaBuda et al, 1996) and the intriguing finding on chromosome 4p of an apparent ‘protective’ locus in the same region where linkage to a susceptibility locus has been identified in other families (Ginns et al, 1998). All of these studies illustrate some of the advantages of working with large families. The penetrance and mode of inheritance may vary between different populations but can often be defined more clearly within one family where information about the presence of anticipation, imprinting and other factors is also likely to be available. It is likely that within a single family the influence of one or a small number of genes will be paramount and hence detectable. However, there are limitations to using large families. Disease in a family may be derived not from one but from several founders, or the disease may be the result of rare genetic causes that explain an insignificant fraction of the condition in a wider population. Despite these limitations, identifying any gene contributing to bipolar illness would be a significant advance and would point to other genes related by sequence or function.


Karyotype abnormalities associated with the development of a medical illness can point directly to chromosomal regions that contain candidate disease genes and have played a key role in the search for genes for many genetic conditions. If the anomaly is inherited, its co-segregation with a specific illness can be tested by linkage. Moreover, if the size of available pedigree is small then the chance of true association is increased if the chromosomal abnormality lies within a region where linkage or association has been previously reported in other families.

A balanced reciprocal chromosomal translocation t(1;11)(q42.1;q14.3) has been found to co-segregate with several major psychiatric disorders, including severe recurrent major depressive disorder and schizophrenia, in a large Scottish pedigree (St Clair et al, 1990). A recent follow-up of this family has identified additional subjects with the translocation who have developed major psychotic illness, including bipolar disorder (Blackwood et al, 1998). Systematic physical mapping of the breakpoints of this translocation has revealed disrupted coding sequences on chromosome 1 that represent candidate genes for the psychoses within this family (Muir et al, 1995; Millar et al, 2000, 2001).

A rare chromosomal abnormality, inv(18)(p11.3;q21.1), has been described in separate Danish and Scottish families (Mors et al, 1997). The inversion is associated with bipolar disorder in one family and schizophrenia in the other. The breakpoints lie within the linkage regions on the long and short arms of chromosome 18 and it may be hypothesised that they have disrupted genes at one or both breakpoints (Hampson et al, 1999).


Model-based linkage analysis in single extended pedigrees requires prior specification of the mode of inheritance, penetrance and population frequency of the trait. Since none of these variables in bipolar disorder is known for certain, a high rate of false positive or negative linkage findings are likely. Recently, there has been renewed interest in variance-based methods to detect QTLs for complex traits (Almasy & Blangero, 1998). These methods do not specify any particular genetic model but identify regions of the genome which explain a significant amount of the phenotypic variation in the trait. These regions are then the best estimates for the location of a QTL. When data from a single large pedigree that showed significant linkage between bipolar disorder and markers on chromosome 4p were re-analysed using a variance component method, the results confirmed that this more robust approach can be successfully used for the analysis of data from a single pedigree (Visscher et al, 1999). The variance component method, unlike linkage analysis, can distinguish between polygenic variation and single-gene effects. In addition, this model can include factors and covariates such as cohort or gender effects and allow other random effects which cause the observations to be correlated, such as a common environmental effect. Furthermore, variance models can be extended to multiple QTLs, making it possible to examine for epistatic interactions between loci in a family, and can be applied also to multiple traits simultaneously.


The dramatic successes of linkage studies in identifying genes for neuropsychiatric disorders, such as Huntington's disease and Alzheimer's disease, have not yet been matched in the affective disorders. Linkage strategies based on affected sibling pairs or many small families have limited power if the disease phenotype can be caused by variation in one of many genes in a population. In diseases with marked allelic complexity much can be learned by examining single large families, even when these show atypical clinical phenotypes. These include inbred or geographically isolated pedigrees, families with chromosomal abnormalities co-segregating with illnesses, and families with mental illness and comorbid conditions such as learning disabilities or deafness. In these families the search for linkage is facilitated because only one or a few loci may be responsible for the trait. To identify even a rare locus could point the way to other causes of bipolar disorder.

Clinical Implications and Limitations


  • Understanding genetic risk factors in bipolar disorder may:

  • Form the basis of a biological classification of the disorder.

  • Guide the search for new drug therapies.

  • Suggest preventative measures.


  • A single family may express an uncommon form of a disease and give findings of limited application to the general population. An example is that of the BRCA genes which explain much of the variance in breast cancer in some affected families but less of the variance in the population as a whole.

  • The resolution for linkage in single families is limited by the relatively small number of meioses available for study: a typical linkage region will be 5-30 centimorgans. Linkage disequilibrium methods which essentially use historical meioses may reduce the mapping resolution to less than 1 centimorgan.

  • Linkage results in extended pedigrees may be confounded by inbreeding or the presence of several founders.


Adams, L. J., Mitchell, P. B., Fielder, S. L., et al (1998) A susceptibility locus for bipolar disorder on chromosome 4q35. American Journal of Human Genetics, 62, 10841091.
Almasy, L. & Blangero, J. (1998) Multipoint quantitative trait linkage analysis in general pedigrees. American Journal of Human Genetics, 62, 11981211.
Armstrong, C., Marshall, D., Todd, R. D., et al (1997) An initial report of a genome screen for a bipolar I disorder susceptibility locus in a large multiplex kindred of Swiss ancestry. American Journal of Medical Genetics (Neuropsychiatric Genetics), 74, 586.
Asherson, P., Mant, R., Williams, N., et al (1998) A study of chromosome 4p markers and dopamine D5 receptor gene in schizophrenia and bipolar disorder. Molecular Psychiatry, 3, 310320.
Barden, N., Plante, M., Rochette, D., et al (1996) Genome wide microsatellite marker linkage study of bipolar affective disorder in a very large pedigree derived from a homogeneous population in Quebec points to a susceptibility locus on chromosome 12. Psychiatric Genetics, 6, 145146.
Blackwood, D. H. R., He, L., Morris, S. W., et al (1996) A locus for bipolar affective disorder on chromosome 4p. Nature Genetics, 12, 427430.
Blackwood, D. H. R., Fordyce, A., Walker, M., et al (1998) Thirty year follow-up of a family showing association of schizophrenia with a balanced translocation t(1:11)(q42.1,q14.3). American Journal of Medical Genetics (Neuropsychiatric Genetics), 81, 532.
Craddock, N., Owen, M., Burge, S., et al (1994) Familial cosegregation of major affective disorder and Darier's disease (keratosis follicularis). British Journal of Psychiatry, 164, 355358.
Ewald, H., Mors, O., Flint, T., et al (1995) A possible locus for manic depressive illness on chromosome 16p13. Psychiatric Genetics, 5, 7181.
Ewald, H., Degn, B., Mors, O., et al (1998a) Support for the possible locus on chromosome 4p16 for bipolar affective disorder. Molecular Psychiatry, 3, 442448.
Ewald, H., Degn, B., Mors, O., et al (1998b) Significant linkage between bipolar affective disorder and chromosome 12q. Psychiatric Genetics, 8, 131140.
Freimer, N. B., Reus, V. I., Escamilla, M. A., et al (1996) Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22–q23. Nature Genetics, 12, 435441.
Ginns, E. I., Ott, J., Egeland, J. A., et al (1996) A genome wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish. Nature Genetics, 12, 431435.
Ginns, E. I., St Jean, P., Philibert, R. A., et al (1998) A genome-wide search for chromosomal loci linked to mental health wellness in relatives at high risk for bipolar affective disorder among the Old Order Amish. Proceedings of the National Academy of Science, 95, 1553115536.
Hampson, R. M., Malloy, M. P., Mors, O., et al (1999) Mapping studies on a pericentric inversion (18) (P11.31 q21.1) in a family with both schizophrenia and learning disabilities. Molecular Psychiatry, 9, 161163.
LaBuda, M. C., Maldonado, M., Marshall, D., et al (1996) A follow-up report of a genome search for affective disorder predisposition loci in the old order Amish. American Journal of Human Genetics, 59, 13431362.
Millar, J. K., Wilson-Annan, J. C., Anderson, S., et al (2000) Disruption of two novel genes by a translocation co-segregating with schizophrenia. Human Molecular Genetics, 9, 14151423.
Millar, J. K., Christie, S., Anderson, S., et al (2001) Genomic structure and localisation within a linkage hotspot of Disrupted in Schizophrenia 1, a gene disrupted by a translocation segregating with schizophrenia. Molecular Psychiatry, 6, 173178.
Morissette, J., Villeneuve, A., Dordeleau, L., et al (1999) Genome-wide search for linkage of Bipolar Affective Disorder in a very large pedigree derived from a homogeneous population in Quebec points to a locus of major effect on chromosome 12q23–24. American Journal of Medical Genetics, 88, 567587.
Mors, O., Ewald, H., Blackwood, D., et al (1997) Cytogenetic abnormalities on chromosome 18 associated with bipolar affective disorder or schizophrenia. British Journal of Psychiatry, 170, 278280.
Muir, W. J., Gosden, C. M., Brookes, A. J., et al (1995) Direct microdissection and microcloning of a translocation breakpoint region t(1; 11)(q42.2;q21) associated with schizophrenia. Cytogenetics and Cell Genetics, 70, 3540.
Pekkarinen, P., Terwilliger, J., Bredbacka, P. E., et al (1995) Evidence of a predisposing locus to bipolar disorder on Xq24–q271 in an extended Finnish pedigree. Genome Research, 5, 105115.
Risch, N. & Botstein, D. (1996) A manic depressive history. Nature Genetics, 12, 351353.
St Clair, D., Blackwood, D., Muir, W., et al (1990) Association within a family of a balanced autosomal translocation with major mental illness. Lancet, 336, 1316.
Straub, R. E., Lehner, T., Luo, Y., et al (1994) A possible vulnerability locus for bipolar affective disorder on chromosome 21q 22.3. Nature Genetics, 8, 291296.
Terwilliger, J. D. & Weiss, K. M. (1998) Linkage disequilibrium mapping of complex disease: fantasy or reality? Current Opinion in Biotechnology, 9, 578594.
Visscher, P. M., Haley, C. S., Heath, S. C., et al (1999) Detecting QTLs for uni- and bipolar disorder using a variance component method. Psychiatric Genetics, 9, 7484.