Based on the literature demonstrating that female smokers in the premenstrual phase of their menstrual cycle (MC) experience greater nicotine-induced withdrawal (WD) and craving, three investigations into the role of the MC phase in smoking cessation treatment were conducted, with the same initial hypothesis: women who attempt to quit smoking while in the pre-ovulatory phase of the MC will achieve greater success than women who make a quit attempt in the premenstrual phase [1-3].
In line with the initial hypothesis, study 1 (Franklin et al.) found that females who started smoking cessation treatment in the pre-ovulatory phase were more than twice as likely as females in the premenstrual phase to achieve an abstinent outcome [1]. Although non-significant, Carpenter et al. reported similar findings [3]. Contrary to the initial hypothesis and the findings of the other studies, a well-controlled, randomized, prospective study conducted by Allen et al. found that premenstrual females had better treatment outcome success compared to pre-ovulatory females [2]. Here we will discuss only the findings of study 1 (Franklin et al. [1]) and study 2 (Allen et al. [2]).
There were several differences between the two studies (see Table 1). However, one in particular may explain the discordant findings. Study 1 included both nicotine replacement (NRT) and behavioral components, while study 2 was strictly a behavioral study. We propose that protection from WD symptoms provided by NRT at treatment initiation may be at the crux of the apparently discrepant findings.
Table 1 Characteristics of the two studies, examining the influence of menstrual cycle (MC) phase at initiation of smoking cessation treatment on treatment outcome |
Our working hypothesis is based partially on the more abundant and consistent preclinical reports demonstrating that addictive drugs are more rewarding during proestrus/estrus, the animal equivalent of the human pre-ovulatory phase [4]. The animal data imply that giving up smoking during the pre-ovulatory phase, when smoking during a lapse would be more rewarding, would eventuate in less favorable treatment outcome. The findings of study 2 are consistent with the animal literature. In study 1, wherein women received NRT, initial lapse rates were reduced in pre-ovulatory females compared to premenstrual females. We suggest that the initial early protection from WD symptoms provided by NRT prevented a lapse from occurring in the pre-ovulatory females in study 1, and therefore prevented the experience of increased reward. In contrast, premenstrual females lapsed, even while protected from WD, possibly a function of the discomfort associated with premenstrual symptoms. In support, although premenstrual compared to pre-ovulatory females were less likely to lapse early in treatment in study 2, the percentage of premenstrual females who were abstinent at the first time-point was similar between studies 1 (48%) and 2 (56%). Further, the numbers of premenstrual females abstinent at end of treatment were similar between studies 1 (29%) and 2 (34%) (see Table 1).
In conclusion, the question may become not only ‘when’ is the best time to quit smoking (pre-ovulatory versus premenstrual) but also ‘how’ (protected from WD symptoms versus unprotected). We acknowledge that an empirical test of our working hypothesis is a double-blind placebo-controlled NRT study wherein females are randomized according to cycle phase. Nevertheless, the findings of these two studies warrant the attention of researchers and clinicians alike.



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