Kenneth S Kendler1,2,3, Henrik Ohlsson4, Jan Sundquist4,5,6, Kristina Sundquist4,5,6. 1. Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA. 2. Department of Psychiatry, Virginia Commonwealth University, RichmondVA, USA. 3. Department of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA, USA. 4. Center for Primary Health Care Research, Lund University, Malmö, Sweden. 5. Department of Family Medicine and Community Health, Department of Population Health Science and Policy, Icahn School of Medicine at Mount Sinai, New York, USA. 6. Center for Community-based Healthcare Research and Education (CoHRE), Department of Functional Pathology, School of Medicine, Shimane University, Japan.
Abstract
BACKGROUND: We introduce and apply an elegant, contrastive genetic-epidemiological design - Maternal Half-Sibling Families with Discordant Fathers - to clarify cross-generational transmission of genetic risk to alcohol use disorder (AUD), drug abuse (DA) and major depression (MD). METHOD: Using Swedish national registries, we identified 73 108 eligible pairs of reared together maternal half-siblings and selected those whose biological fathers were discordant for AUD, DA and MD, and had minimal contact with the affected father. We examined differences in outcome in half-siblings with an affected v. unaffected father. RESULTS: For AUD, DA and MD, the HR (95% confidence intervals) for the offspring of affected v. unaffected fathers were, respectively, 1.72 (1.61; 1.84), 1.55 (1.41; 1.70) and 1.51 (1.40; 1.64). Paternal DA and AUD, but not MD, predicted risk in offspring for attention deficit hyperactivity disorder, conduct disorder, and poor educational performance and attainment. Offspring of affected v. unaffected fathers had poorer pregnancy outcomes, with the effect strongest for DA and weakest for MD. A range of potential biases and confounders were examined and were not found to alter these findings substantially. CONCLUSION: Reared together maternal half-siblings differ in their paternal genetic endowment, sharing the same mother, family, school and community. They can help clarify the nature of paternal genetic effects and produce results consistent with other designs. Paternal genetic risk for DA and AUD have effects on offspring educational achievement, child and adult psychopathology, and possibly prenatal development. The impact of paternal genetic risk for MD is narrower in scope.
BACKGROUND: We introduce and apply an elegant, contrastive genetic-epidemiological design - Maternal Half-Sibling Families with Discordant Fathers - to clarify cross-generational transmission of genetic risk to alcohol use disorder (AUD), drug abuse (DA) and major depression (MD). METHOD: Using Swedish national registries, we identified 73 108 eligible pairs of reared together maternal half-siblings and selected those whose biological fathers were discordant for AUD, DA and MD, and had minimal contact with the affected father. We examined differences in outcome in half-siblings with an affected v. unaffected father. RESULTS: For AUD, DA and MD, the HR (95% confidence intervals) for the offspring of affected v. unaffected fathers were, respectively, 1.72 (1.61; 1.84), 1.55 (1.41; 1.70) and 1.51 (1.40; 1.64). Paternal DA and AUD, but not MD, predicted risk in offspring for attention deficit hyperactivity disorder, conduct disorder, and poor educational performance and attainment. Offspring of affected v. unaffected fathers had poorer pregnancy outcomes, with the effect strongest for DA and weakest for MD. A range of potential biases and confounders were examined and were not found to alter these findings substantially. CONCLUSION: Reared together maternal half-siblings differ in their paternal genetic endowment, sharing the same mother, family, school and community. They can help clarify the nature of paternal genetic effects and produce results consistent with other designs. Paternal genetic risk for DA and AUD have effects on offspring educational achievement, child and adult psychopathology, and possibly prenatal development. The impact of paternal genetic risk for MD is narrower in scope.
Entities:
Keywords:
Alcohol use disorder; depression; drug abuse; genetic epidemiology
Authors: Kenneth S Kendler; Hermine H Maes; Kristina Sundquist; Henrik Ohlsson; Jan Sundquist Journal: Am J Psychiatry Date: 2014-02 Impact factor: 18.112
Authors: Raymond K Walters; Renato Polimanti; Emma C Johnson; Jeanette N McClintick; Mark J Adams; Amy E Adkins; Fazil Aliev; Silviu-Alin Bacanu; Anthony Batzler; Sarah Bertelsen; Joanna M Biernacka; Tim B Bigdeli; Li-Shiun Chen; Toni-Kim Clarke; Yi-Ling Chou; Franziska Degenhardt; Anna R Docherty; Alexis C Edwards; Pierre Fontanillas; Jerome C Foo; Louis Fox; Josef Frank; Ina Giegling; Scott Gordon; Laura M Hack; Annette M Hartmann; Sarah M Hartz; Stefanie Heilmann-Heimbach; Stefan Herms; Colin Hodgkinson; Per Hoffmann; Jouke Jan Hottenga; Martin A Kennedy; Mervi Alanne-Kinnunen; Bettina Konte; Jari Lahti; Marius Lahti-Pulkkinen; Dongbing Lai; Lannie Ligthart; Anu Loukola; Brion S Maher; Hamdi Mbarek; Andrew M McIntosh; Matthew B McQueen; Jacquelyn L Meyers; Yuri Milaneschi; Teemu Palviainen; John F Pearson; Roseann E Peterson; Samuli Ripatti; Euijung Ryu; Nancy L Saccone; Jessica E Salvatore; Sandra Sanchez-Roige; Melanie Schwandt; Richard Sherva; Fabian Streit; Jana Strohmaier; Nathaniel Thomas; Jen-Chyong Wang; Bradley T Webb; Robbee Wedow; Leah Wetherill; Amanda G Wills; Jason D Boardman; Danfeng Chen; Doo-Sup Choi; William E Copeland; Robert C Culverhouse; Norbert Dahmen; Louisa Degenhardt; Benjamin W Domingue; Sarah L Elson; Mark A Frye; Wolfgang Gäbel; Caroline Hayward; Marcus Ising; Margaret Keyes; Falk Kiefer; John Kramer; Samuel Kuperman; Susanne Lucae; Michael T Lynskey; Wolfgang Maier; Karl Mann; Satu Männistö; Bertram Müller-Myhsok; Alison D Murray; John I Nurnberger; Aarno Palotie; Ulrich Preuss; Katri Räikkönen; Maureen D Reynolds; Monika Ridinger; Norbert Scherbaum; Marc A Schuckit; Michael Soyka; Jens Treutlein; Stephanie Witt; Norbert Wodarz; Peter Zill; Daniel E Adkins; Joseph M Boden; Dorret I Boomsma; Laura J Bierut; Sandra A Brown; Kathleen K Bucholz; Sven Cichon; E Jane Costello; Harriet de Wit; Nancy Diazgranados; Danielle M Dick; Johan G Eriksson; Lindsay A Farrer; Tatiana M Foroud; Nathan A Gillespie; Alison M Goate; David Goldman; Richard A Grucza; Dana B Hancock; Kathleen Mullan Harris; Andrew C Heath; Victor Hesselbrock; John K Hewitt; Christian J Hopfer; John Horwood; William Iacono; Eric O Johnson; Jaakko A Kaprio; Victor M Karpyak; Kenneth S Kendler; Henry R Kranzler; Kenneth Krauter; Paul Lichtenstein; Penelope A Lind; Matt McGue; James MacKillop; Pamela A F Madden; Hermine H Maes; Patrik Magnusson; Nicholas G Martin; Sarah E Medland; Grant W Montgomery; Elliot C Nelson; Markus M Nöthen; Abraham A Palmer; Nancy L Pedersen; Brenda W J H Penninx; Bernice Porjesz; John P Rice; Marcella Rietschel; Brien P Riley; Richard Rose; Dan Rujescu; Pei-Hong Shen; Judy Silberg; Michael C Stallings; Ralph E Tarter; Michael M Vanyukov; Scott Vrieze; Tamara L Wall; John B Whitfield; Hongyu Zhao; Benjamin M Neale; Joel Gelernter; Howard J Edenberg; Arpana Agrawal Journal: Nat Neurosci Date: 2018-11-26 Impact factor: 24.884