Literature DB >> 7762550

Patterns of maternal transmission in bipolar affective disorder.

F J McMahon1, O C Stine, D A Meyers, S G Simpson, J R DePaulo.   

Abstract

The mode of inheritance of bipolar affective disorder (BPAD) appears complex, and non-Mendelian models of inheritance have been postulated. Two non-Mendelian phenomena, genomic imprinting and mitochondrial inheritance, may contribute to the complex inheritance pattern seen in BPAD. Both imprinting and mitochondrial inheritance share the feature of differential expression of the phenotype, depending on the parent of origin. In this study we tested the hypothesis of a parent-of-origin effect on the transmission of BPAD. We examined the frequency and risk of affective disorder among relatives in a sample of 31 families ascertained through treated probands with BPAD and selected for the presence of affected phenotypes in only one parental lineage. Three specific comparisons were performed: (1) the observed frequency of transmitting mothers versus transmitting fathers; (2) the observed frequency and lifetime risk of BPAD among the maternal versus the paternal relatives of probands; and (3) the observed frequency and lifetime risk of BPAD for the offspring of affected mothers compared with the offspring of affected fathers. We observed a higher than expected frequency of affected mothers (P < .04), a 2.3-2.8-fold increased risk of illness for maternal relatives (P < .006), and a 1.3- 2.5-fold increased risk of illness for the offspring of affected mothers (P < .017). In seven enlarged pedigrees, fathers repeatedly failed to transmit the affected phenotype to daughters or sons. Taken together, these findings indicate a maternal effect in the transmission of BPAD susceptibility and suggest that molecular studies of mtDNA and imprinted DNA are warranted in patients with BPAD.

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Year:  1995        PMID: 7762550      PMCID: PMC1801083     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  42 in total

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  46 in total

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Authors:  Glenn A Doyle; John P Dahl; Paul J Bloch; Andrew E Weller; Falk W Lohoff; Thomas N Ferraro; Wade H Berrettini
Journal:  Psychiatr Genet       Date:  2011-02       Impact factor: 2.458

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10.  A novel class of tests for the detection of mitochondrial DNA-mutation involvement in diseases.

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Journal:  Am J Hum Genet       Date:  2003-04-30       Impact factor: 11.025

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