Premature Ejaculation Research
Premature Ejaculation Research History
MD Waldinger, one of the leading researcher on the subject, split the history of Premature Ejaculation Research into four periods1. Its period scientific literature influences each period. Therefore, each period specialists postulated different causes for premature ejaculation.
Urological / Psychological Period
Karl Abraham wrote one of the first major scientific work on PE in 19172. During those years, Abraham speculated that unconscious psychological conflicts caused premature ejaculation. Still, some of the cases were believed to be caused by urological and anatomical factors such as a hypersensitivity of the penis skin or a too short frenulum2,3.
In the 40s, Bernhard Schapiro, a German endocrinologist, was the first to divide premature ejaculation into two subtypes4. Those subtypes became years later what we know as the lifelong PE and the acquire PE. The first subtype represents those who always ejaculated quickly while the second those who gain the condition during their life.
In the 70s, William Masters and Virginia Johnson proposed a behavioral explanation to Premature Ejaculation5. Their theory explained PE as a learning behavior. They suspected that men who lack ejaculation control never learned how to control their arousal. They thought that quick first sexual experience could create an habituation to rapid ejaculation. Thereupon, this habituation can lead to performance anxiety. A lot of focus has been placed on the anxiety aspect in the following years. Therefore, psychological explanations of PE has eclipsed the organic ones for a while.
The delay effect on ejaculation of certain prescription drugs has led researchers of the 80s and 90s into neurological explanations of PE. In 1998, Waldinger and his team were the first to propose a neurologic explanation for lifelong PE6. Therefore, they rejected the purely psychological and behavioristic view for this specific subtype of premature ejaculation. For Waldinger, lifelong PE is caused by biological and genetic factors that are probably hereditary.
This period marks the arrival of prescribed drugs as a recommended treatment for Premature Ejaculation.
Genetics and Pharmaceutical Period
Today’s research is aimed at genetics, neurology, and endocrinology (the study of hormones). The pharmaceutical industry, just like they did with erectile dysfunction, perceived a business opportunity and became interested in PE. Therefore, the financing of scientific studies (almost inexistent before the 90s) increased substantially.
This period also marks the first evidence-based definition of Premature ejaculation. Before 2008, there was no strict definition of PE. Therefore, each study used their own selection criteria. The ISSM organized a meeting with all the experts on Premature Ejaculation in 2007 to make sure everybody agrees on what is premature ejaculation. Following this meeting, the ISSM set some strict criteria for the lifelong PE (ejaculation must always occur within 1 minute of vaginal penetration).
However, since the definition excluded most of the men that complain about their ejaculation control, two other subtypes have been created: variable PE and Subjective PE. Variable PE includes men who sometimes ejaculate within one minute, but not always. Subjective PE contains men who aren’t happy about their ejaculation control but are still over the 1 minute period. More information on these subtypes can be found on the What is Premature Ejaculation page.
Current State of Premature Ejaculation
The fact that each therapist or each researcher had their own definition of premature ejaculation is probably one of the reasons why premature ejaculation researchers have often been contradictory.
Now that Premature Ejaculation is split into four subtypes, research can be more focused. Specialists like Waldinger suspects that lifelong PE has more organic/biological factors while other subtypes more psychological/behavioral ones. This split could explain the difference between each period explanation of premature ejaculation.
With more research coming in the next year, more treatment options (medical or not) should become available.
- Waldinger MD (2004) Lifelong premature ejaculation: from authority-based to evidence based medicine. Brit J Urol Int 93:201–207
- Abraham K (1917) Über Ejaculatio Praecox. Zeitschr Aerztliche Psychoanalyse 4:171-186
- Stekel W (1927) Impotence in the male. The psychic disorders of sexual function in the male. Boni & Liveright Publ Corp, New York, 2:22–60
- Schapiro B (1943) Premature ejaculation: a review of 1130 cases. J Urol 50:374–379
- Masters WH, Johnson VE (1970) Premature ejaculation. In: Masters WH, Johnson VE (eds) Human sexual inadequacy. Little, Brown and Co, Boston
- Waldinger MD, Berendsen HHG, Blok BFM, Olivier B, Holstege G (1998) Premature ejaculation and serotonergic antidepressants-induced delayed ejaculation: the involvement of the serotonergic system. Behav Brain Res 92:111–118, Waldinger MD, Rietschel M, Nothen MM, Hengeveld MW, Olivier B (1998) Familial occurrence of primary premature ejaculation. Psychiatr Gen 8:37–40