Abstract
In 1998, it was suggested that the intravaginal ejaculation latency time (IELT) in men with lifelong premature ejaculation (PE) is influenced by neurobiological and genetic factors. Although a familial occurrence of PE has been suggested in 1943 and later also has been investigated in a family study in 1998, there is no real hard evidence today to suggest that being a first-degree relative of a man with lifelong PE is a risk factor for PE. Notably, family studies on PE remain difficult to perform owing to the existing taboo to talk on PE. On the other hand, in 2007, a Finnish twin study suggested a moderate genetic effect on PE in the general male population, but risk factors where not identified. In 2009, a quantified case-control association study in Dutch men with lifelong PE showed that polymorphism of the 5-HT transporter is associated with the IELT in men who ejaculate within 1 min. But based on this study, one can not conclude that having the LL-genotype of this polymorphism is a risk factor for PE. Recently, four premature ejaculation (PE) subtypes have been distinguished on the basis of the duration of the IELT. These four PE subtypes have a different etiology and pathogenesis. Genetic research of PE should consider the existence of these PE subtypes and the accurate measurement of the IELT with a stopwatch.
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Waldinger, M.D. (2013). Risks Factors in Premature Ejaculation: The Genetic Risk Factor. In: Jannini, E., McMahon, C., Waldinger, M. (eds) Premature Ejaculation. Springer, Milano. https://doi.org/10.1007/978-88-470-2646-9_9
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DOI: https://doi.org/10.1007/978-88-470-2646-9_9
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