From sperm to offspring: Assessing the heritable genetic consequences of paternal smoking and potential public health impacts.
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TL;DR: The available evidence makes a compelling case that tobacco smoke is a human germ cell mutagen with serious public health and socio-economic implications, and increased public education should be encouraged to promote abstinence from smoking, well in advance of reproduction, to minimize the transmission of harmful mutations to the next-generation.
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Abstract: Individuals who smoke generally do so with the knowledge of potential consequences to their own health. What is rarely considered are the effects of smoking on their future children. The objective of this work was to review the scientific literature on the effects of paternal smoking on sperm and assess the consequences to offspring. A literature search identified over 200 studies with relevant data in humans and animal models. The available data were reviewed to assess the weight of evidence that tobacco smoke is a human germ cell mutagen and estimate effect sizes. These results were used to model the potential increase in genetic disease burden in offspring caused by paternal smoking, with specific focus on aneuploid syndromes and intellectual disability, and the socioeconomic impacts of such an effect. The review revealed strong evidence that tobacco smoking is associated with impaired male fertility, and increases in DNA damage, aneuploidies, and mutations in sperm. Studies support that these effects are heritable and adversely impact the offspring. Our model estimates that, with even a modest 25% increase in sperm mutation frequency caused by smoke-exposure, for each generation across the global population there will be millions of smoking-induced de novo mutations transmitted from fathers to offspring. Furthermore, paternal smoking is estimated to contribute to 1.3 million extra cases of aneuploid pregnancies per generation. Thus, the available evidence makes a compelling case that tobacco smoke is a human germ cell mutagen with serious public health and socio-economic implications. Increased public education should be encouraged to promote abstinence from smoking, well in advance of reproduction, to minimize the transmission of harmful mutations to the next-generation.
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Citations
Lifestyle causes of male infertility.
TL;DR: The major lifestyle factors discussed in the present review are amongst the multiple potential risk factors that could impair male fertility, however, their negative impact may well be mostly overcome by behaviour modification and better lifestyle choices.
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The present crisis in male reproductive health: an urgent need for a political, social, and research roadmap.
TL;DR: Couples are increasingly utilizing IVF at more advanced ages, and advanced paternal age is associated with increased risk for adverse perinatal outcomes for both offspring and mother; (ii) early child mortality, cancer, and mental health issues.
Paternal age: Negative impact on sperm genome decays and IVF outcomes after 40 years.
Ismail Kaarouch,Nouzha Bouamoud,Aicha Madkour,Noureddine Louanjli,Brahim Saadani,Said Assou,Smahane Aboulmaouahib,Saaïd Amzazi,Henri Copin,Moncef Benkhalifa,Omar Sefrioui +10 more
TL;DR: Analysis of the results suggests that the age of 40 should be considered as the APA cutoff during ART attempts, as indicated by the rates of cancelled embryo transfers, clinical pregnancy and miscarriage in the two groups APA and Y.
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The Role of Genetics and Oxidative Stress in the Etiology of Male Infertility-A Unifying Hypothesis?
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TL;DR: A hypothesis is presented whereby a number of environmental, lifestyle and clinical factors conspire to induce oxidative DNA damage in the male germ line which then triggers the formation of de novo mutations which can have a major impact on the health of the offspring including their subsequent fertility.
Role of miRNA in the Transmission of Metabolic Diseases Associated With Paternal Diet-Induced Obesity
TL;DR: The concept of Developmental Origins of Health and Diseases (DOHaD) recognizes that an unfavorable maternal environment alters the developmental trajectory of the fetus and can lead to long-term risk of developing chronic noncommunicable diseases.
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Brian J. O'Roak,Pelagia Deriziotis,Pelagia Deriziotis,Choli Lee,Laura Vives,Jerrod J. Schwartz,Santhosh Girirajan,Emre Karakoc,Alexandra P. MacKenzie,Sarah B. Ng,Carl Baker,Mark J. Rieder,Deborah A. Nickerson,Raphael Bernier,Simon E. Fisher,Simon E. Fisher,Simon E. Fisher,Jay Shendure,Evan E. Eichler,Evan E. Eichler +19 more
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The C9orf72 GGGGCC Repeat Is Translated into Aggregating Dipeptide-Repeat Proteins in FTLD/ALS
Kohji Mori,Shih-Ming Weng,Thomas Arzberger,Stephanie May,Kristin Rentzsch,Elisabeth Kremmer,Bettina Schmid,Bettina Schmid,Hans A. Kretzschmar,Marc Cruts,Christine Van Broeckhoven,Christian Haass,Christian Haass,Dieter Edbauer,Dieter Edbauer +14 more
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Costs of Autism Spectrum Disorders in the United Kingdom and the United States
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Marcus Pembrey,Marcus Pembrey,Lars Olov Bygren,Lars Olov Bygren,Gunnar Kaati,Sören Edvinsson,Kate Northstone,Michael Sjöström,Jean Golding +8 more
TL;DR: It is concluded that sex-specific, male-line transgenerational responses exist in humans and hypothesise that these transmissions are mediated by the sex chromosomes, X and Y and add an entirely new dimension to the study of gene–environment interactions in development and health.
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