Literature DB >> 1443242

Assessment of lineality in bipolar I linkage studies.

S G Simpson1, S E Folstein, D A Meyers, J R DePaulo.   

Abstract

OBJECTIVE: To assess lineality in families of bipolar I probands, the authors used direct interviews of family members to reclassify families initially categorized as unilineal by family history.
METHOD: The families of 1,800 treated bipolar I probands were screened by the family history method with multiple informants. If the proband had one or more affected sibs and one apparently unaffected parent, the parents (and then other available first- and second-degree relatives) were directly interviewed by psychiatrists.
RESULTS: Of the 1,800 families screened, 56 were apparently suitable unilineal families with multiple affected members; 46 families were interviewed directly. After interviews with the parents, 12 families (26.1%) were found to be bilineal. Direct interviews of all available relatives in the 34 remaining families revealed that only 22 (47.8% of the 46 interviewed families) were unilineal or probably unilineal and 12 were probably bilineal. The probably bilineal families had a significantly higher proportion of siblings with unipolar disorder. In addition, the affected sibs from the probably bilineal families tended to have earlier onsets but had significantly fewer symptoms in the most severe depressive episode.
CONCLUSIONS: Fewer than 50% of bipolar I families appearing unilineal according to family history were found to be unilineal by direct interviews. The phenotypic differences between the affected sibs from the probably bilineal families and those from the unilineal and probably unilineal families suggest differences in genetic mechanisms. These findings highlight the need to systematically assess lineality in all families considered for bipolar I linkage studies and support the preferential inclusion of unilineal families in linkage studies.

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Year:  1992        PMID: 1443242     DOI: 10.1176/ajp.149.12.1660

Source DB:  PubMed          Journal:  Am J Psychiatry        ISSN: 0002-953X            Impact factor:   18.112


  8 in total

1.  Full-genome scan for linkage in 50 families segregating the bipolar affective disease phenotype.

Authors:  C Friddle; R Koskela; K Ranade; J Hebert; M Cargill; C D Clark; M McInnis; S Simpson; F McMahon; O C Stine; D Meyers; J Xu; D MacKinnon; T Swift-Scanlan; K Jamison; S Folstein; M Daly; L Kruglyak; T Marr; J R DePaulo; D Botstein
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

2.  Linkage of bipolar affective disorder to chromosome 18 markers in a new pedigree series.

Authors:  F J McMahon; P J Hopkins; J Xu; M G McInnis; S Shaw; L Cardon; S G Simpson; D F MacKinnon; O C Stine; R Sherrington; D A Meyers; J R DePaulo
Journal:  Am J Hum Genet       Date:  1997-12       Impact factor: 11.025

3.  More assortative mating in US compared to European parents and spouses of patients with bipolar disorder: implications for psychiatric illness in the offspring.

Authors:  Robert M Post; Lori L Altshuler; Ralph Kupka; Susan L McElroy; Mark A Frye; Michael Rowe; Heinz Grunze; Trisha Suppes; Paul E Keck; Willem A Nolen
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  2018-08-11       Impact factor: 5.270

4.  Patterns of maternal transmission in bipolar affective disorder.

Authors:  F J McMahon; O C Stine; D A Meyers; S G Simpson; J R DePaulo
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025

5.  Anticipation in bipolar affective disorder.

Authors:  M G McInnis; F J McMahon; G A Chase; S G Simpson; C A Ross; J R DePaulo
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

6.  Brain serotonin transporter binding in depressed patients with bipolar disorder using positron emission tomography.

Authors:  Maria A Oquendo; Ramin S Hastings; Yung-Yu Huang; Norman Simpson; R Todd Ogden; Xian-Zhang Hu; David Goldman; Victoria Arango; Ronald L Van Heertum; J John Mann; Ramin V Parsey
Journal:  Arch Gen Psychiatry       Date:  2007-02

7.  Evidence for linkage of bipolar disorder to chromosome 18 with a parent-of-origin effect.

Authors:  O C Stine; J Xu; R Koskela; F J McMahon; M Gschwend; C Friddle; C D Clark; M G McInnis; S G Simpson; T S Breschel; E Vishio; K Riskin; H Feilotter; E Chen; S Shen; S Folstein; D A Meyers; D Botstein; T G Marr; J R DePaulo
Journal:  Am J Hum Genet       Date:  1995-12       Impact factor: 11.025

8.  Treatment of psychiatric symptoms among offspring of parents with bipolar disorder.

Authors:  Isheeta Zalpuri; Manpreet K Singh
Journal:  Curr Treat Options Psychiatry       Date:  2017-11-04
  8 in total

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