Skip to main content
UKPMC Funders Author Manuscripts logoLink to UKPMC Funders Author Manuscripts
. Author manuscript; available in PMC: 2011 May 10.
Published in final edited form as: J Womens Health (Larchmt). 2010 Mar;19(3):391–396. doi: 10.1089/jwh.2008.1210

Lifestyle factors, hormonal contraceptives and premenstrual symptoms: The UK Southampton Women’s Survey

Carrie Sadler 1, Helen Smith 2, Julia Hammond 3, Rosie Bayly 3, Sharon Borland 3, Nick Panay 4, David Crook 2, Hazel Inskip 3; Southampton Women’s Survey Study Group
PMCID: PMC3091016  EMSID: UKMS35211  PMID: 20156129

Abstract

Objective

To estimate the prevalence of premenstrual symptoms in women from the general population in Southampton, UK, and examine their association with lifestyle factors and contraceptive usage.

Design

Cross-sectional survey.

Setting

The City of Southampton, UK.

Population

974 women aged 20-34 years (53% of the 1,841 women invited to participate).

Methods

Interviews, questionnaires and completion of a prospective six-week menstrual symptom diary recording on a daily basis the presence and severity of eleven common premenstrual symptoms.

Main outcome measures

Premenstrual symptoms were identified from the diaries by two clinicians who reviewed them independently using a pre-defined algorithm to assess the onset and decline of symptoms in relation to the start of menstruation.

Results

24% of the women were considered to have premenstrual symptoms (95% confidence interval [CI] 21% to 27%). Women were less likely to have symptoms if they had higher levels of educational attainment and suffered less from stress. No associations were found between premenstrual symptoms and diet, alcohol or strenuous exercise, nor after adjustment for other factors, with age, smoking or body mass index. Use of any form of hormonal contraceptives was associated with a lower prevalence of premenstrual symptoms (prevalence ratio 0.66 (95%CI:0.52 to 0.84)).

Conclusions

Premenstrual symptoms were common in this cohort. Use of hormonal contraceptive methods was associated with a lower prevalence of these symptoms.

Introduction

Data from the US 2002 National Health Interview Survey indicate that 19% of young women have premenstrual syndrome (PMS) or other menstrual-related problems1. Women with PMS often report cyclical symptoms that can either be psychological, such as irritability, or physical, such as headaches and back pain2. These conditions can impact on quality of life3, affecting relationships both at work and home2.

Premenstrual symptoms have been linked to anxiety and depression1 and are associated both with direct medical costs as well as indirect costs due to absenteeism and low productivity in the workplace3,4. There may be substantial public health implications, as women with premenstrual symptoms are more likely to smoke tobacco, drink alcohol and be overweight1.

The etiology of premenstrual symptoms is uncertain. An interaction between the neuroendocrine system and a woman’s sensitivity to the changes in plasma levels of steroid hormones such as estradiol and progesterone are thought to be important5. A wide range of different treatment regimes including lifestyle, complementary and drug therapies have been advocated for the specific disorders of premenstrual syndrome (PMS) and premenstrual dysphoric disorder (PMDD)6-8. Examples of complementary therapies include Vitamin B69 and cognitive behavior therapy10. Selective serotonin reuptake inhibitors have been shown to be effective given both continuously and cyclically11,12. Cyclical progesterone therapy has been advocated13 but multiple trials and meta-analyses have shown progesterone to be ineffective14,15, although these studies mainly looked at cyclical use of progesterone rather than continuous use. Estrogen, delivered either as patches or implants has been shown in several studies to help PMS16,17. In addition, recent studies have shown a positive outcome with combined oral contraceptives containing drospirenone given either cyclically or as a 168 day extended regime18-20.

The Southampton Women’s Survey21 (SWS) is a study of 12,500 young women primarily aimed at unraveling the determinants of the growth and development of their children. Data have been collected on factors such as employment, socio-demographic status, age, ethnicity, physical activity and diet. In this sub-study we have used a menstrual symptom diary in an attempt to identify women within this cohort who have premenstrual symptoms, and then to search for associations with lifestyle factors and contraceptive use.

Materials and Methods

Participants in the SWS were recruited via their General Practitioners (GPs), a profession equivalent to family doctors in the US. A home visit by a research nurse allowed us to obtain data on sociodemographic status, lifestyle, body composition, educational qualifications, ethnicity and diet. We also obtained detailed information on contraceptive use. Following this initial interview, women were invited to provide a blood sample for measurement of a number of parameters for the main study. In October 2001, towards the end of the blood-sampling phase, the premenstrual symptoms sub-study was started. All 1,841 women attending from then until the end of the phase in February 2003, were asked whether they would be interested in taking part in this sub-study. These participants were asked to complete a six-week menstrual symptom diary (a modified version of the validated Moos Menstrual Distress Questionnaire22) in addition to the standard interviews and questionnaires.

Educational grades in the UK are not easily converted to their USA equivalents. We used five categories of qualifications ranging from category 1 (approximating Grade School), category 3 (High School Diploma) and category 5 (Bachelor’s Degree or above). Diet in the SWS was assessed using a 100-item food frequency questionnaire, previously analyzed using principal components analysis23. The first principal component can be interpreted as a summary of the degree to which each woman follows healthy eating recommendations. This has been termed the ‘prudent diet score’ and is used here to assess associations between premenstrual symptoms and a healthy diet.

The menstrual questionnaire recorded the presence and severity of 11 common premenstrual symptoms: irritability, loss of efficiency, difficulty concentrating, tiredness, mood swings, tension, depression, headaches, food craving, acne and fluid retention (breast tenderness, weight gain or swollen/bloated). Two GPs (CS and RB) independently assessed these diaries using criteria developed following a review of definitions of the premenstrual syndrome and premenstrual dysphoric disorder2,24.

Our definition of premenstrual symptoms was made according to the following criteria:

  1. a pattern of symptoms occurring in the days leading up to menstruation that resolved completely or greatly improved by the end of menstruation,

  2. an interval of ≥ 7 days before symptoms recurred, and

  3. ≥ 5 symptoms scored as mild or moderate or ≥ 2 symptoms scored as severe, with each symptom following the pattern described above.

The two GPs independently scored each diary as: 1 (no premenstrual symptoms), 2 (possible symptoms) or 3 (definite symptoms). Where one scored 3 and the other scored 1, the diary was reviewed independently by both GPs and their scores revised if appropriate. In cases of continued disagreement, the GPs met with an arbitrator (HI) to decide on the final score. The scores from the two GPs were added together giving total scores ranging from 2 to 6. Women with scores of 5 or 6 were classified as having premenstrual symptoms, while women with scores equal to or less than 4 were classified as having insufficient symptoms to meet the case definition. As our method does not consider women over a number of cycles and we have no information on the effect of symptoms on daily living, our definition does not conform to formal definitions of premenstrual syndrome7,8,25 and hence our use of the term ‘premenstrual symptoms’.

The data analysis was performed by examining the differences between women with and without premenstrual symptoms. Tabulations and Student’s t-tests were used to explore categorical and continuous variables respectively. Prevalence ratios were calculated using a generalized linear model with a log link and a binomial error structure (binomial regression)26. When the prevalence of the outcome is common, odds ratios derived from a logistic regression cannot be interpreted as approximations to prevalence ratios; this modeling approach provides direct estimates of prevalence ratios. The risk factors identified a priori as possibly linked to premenstrual symptoms were age, educational attainment, smoking status, alcohol consumption, body mass index (BMI), contraceptive use, taking strenuous exercise, reported level of stress, and the type of diet consumed. These data were explored initially in a univariate analysis. Subsequently we developed a multiple regression model by adding variables in a forward step-wise way according to the level of significance in preceding models. The process was considered complete when no further variables could be added such that they made a significant contribution to the model at the 5% level.

Results

Of the 1,841 women asked to participate in this study, 974 (53%) returned a menstrual symptom diary, of which 44 were incomplete and one was found to be outside the age range for the study. Analysis of the diaries led to identification of premenstrual symptoms in 224 women (24%, 95% confidence interval [CI] 21 to 27%). These women had a mean GP coding score of 5.6 compared to a mean score of 2.1 for the remaining women who were classified as having no premenstrual symptoms. If none of the 912 women who did not return a complete diary had met the criteria then the prevalence of premenstrual symptoms in this cohort would have been 12%. We compared the characteristics of responders to the full SWS study population (Table 1) to look for non-response bias, as women with premenstrual symptoms may be more likely to participate than non-sufferers. Participants in this sub-study tended to be somewhat older and better educated than the full study population but the degree of perceived stress was similar. Slightly more of the responders were hormonal contraceptive users, but the proportions taking progestins were similar. Such differences might have a small impact on our overall assessment of prevalence of premenstrual symptoms but should not unduly affect the internal comparisons examining the risk factors. For the risk factor analyses we have excluded a further 71 women who had no discernable menstrual cycle.

Table 1.

Characteristics of the women who completed the menstrual symptom diaries compared with the entire Southampton Women’s Survey cohort.

Characteristic Those completing
menstrual diaries
Entire SWS cohort1
Age (years)
 <25 142 (15.3%) 3,333 (26.6%)
 25-29 309 (33.3%) 4,319 (34.4%)
 30-34 478 (51.5%) 4,899 (39.0%)
Age at initial interview in years [mean (SD)] 29.6 (3.8) 28.2 (4.2)
Highest educational attainment2 n (%)
 I (lowest level) 106 (11.5%) 2,107 (16.9%)
 2 228 (24.8%) 3,313 (26.5%)
 3 320 (34.7%) 3,729 (29.9%)
 4 54 (5.9%) 724 (5.8%)
 5 (highest level) 213 (23.1%) 2,613 (20.9%)
Number currently smoking (%) 174 (18.8%) 3,858 (30.8%)
BMI kg/m2 [median (interquartile range)] 24.5 (22.3-27.7) 24.1 (21.8-27.5)
Reported extent to which stress has affected life
 None 229 (24.7%) 2,841 (22.7%)
 Slightly 357 (38.4%) 4,721 (37.7%)
 Moderately 183 (19.7%) 2,357 (18.8%)
 Quite a lot 135 (14.5%) 2,131 (17.0%)
 Extremely 25 (2.7%) 468 (3.7%)
Contraceptive type 3
 None 443 (49.1%) 3,096 (51.6%)
 Combined OC 379 (42.0%) 2,359 (39.3%)
 Progestin-only pill, etonogestrel, levonorgestrel 47 (5.2%) 291 (4.9%)
 Injectable progestins 34 (3.8%) 257 (4.3%)
White ethnic group 907 (97.7%) 11,785 (94.1%)
In receipt of social security benefits 128 (13.8%) 2,204 (17.6%)
1

Frequencies do not necessarily sum to the same totals due to missing data.

2

Educational levels are explained in the methods section of the paper.

3

Data on contraceptive type was not requested from the women in the earlier part of the SWS, so these data are only available for 6003 women.

In univariate analyses, women with premenstrual symptoms tended to be older, have a lower level of educational achievement, were more likely to smoke, have a higher body mass index (BMI), and a higher perceived level of stress (Table 2). There was no significant difference between those with premenstrual symptoms and those without symptoms with respect to their ‘prudent diet score’, alcohol intake or level of strenuous exercise (data not shown).

Table 2.

Prevalence of premenstrual symptoms in relation to lifestyle factors in the Southampton Women’s Survey. Variables are listed where univariate analysis showed a significant association with premenstrual symptoms at the 5% level of significance. Total numbers studied for each risk factor vary due to missing data. 71 women with no discernable menstrual cycle have been excluded from the analysis.

Variable Number
studied
Number and prevalence (%)
of premenstrual symptoms
Prevalence ratio (95% CI)
(univariate analysis)
Prevalence ratio (95%CI)
(final multivariate model)
Age group (y)
 <25 133 22 (17%) 1 (baseline)
 25-29 287 78 (27%) 1.64 (1.07 to 2.52)
 30-34 438 124 (28%) 1.71 (1.14 to 2.58)
Ptrend = 0.02
Educational qualifications
 I (lowest level) 98 33 (34%) 1 (baseline) 1 (baseline)
 2 205 59 (29%) 0.85 (0.60 to 1.21) 0.82 (0.58 to 1.15)
 3 297 78 (26%) 0.78 (0.56 to 1.09) 0.75 (0.54 to 1.05)
 4 52 12 (23%) 0.69 (0.39 to 1.21) 0.63 (0.35 to 1.13)
 5 (highest level) 199 41 (21%) 0.61 (0.41 to 0.90) 0.60 (0.40 to 0.88)
Ptrend = 0.01 Ptrend = 0.01
Current smoker
 No 702 172 (25%) 1 (baseline)
 Yes 154 52 (34%) 1.38 (1.07 to 1.78)
BMI group (kg/m2)
 <20 42 7 (17%) 0.67 (0.33 to 1.35)
 20-24.99 435 108 (25%) 1 (baseline)
 25-29.99 230 60 (26%) 1.05 (0.80 to 1.38)
 30-34.99 99 29 (29%) 1.18 (0.83 to 1.67)
 ≥35 44 18 (41%) 1.65 (1.11 to 2.44)
Ptrend = 0.01
Reported extent to which stress has affected life
 None 208 43 (21%) 1 (baseline) 1 (baseline)
 Slightly 333 88 (26%) 1.28 (0.93 to 1.76) 1.42 (1.02 to 1.98)
 Moderately 171 50 (29%) 1.41 (0.99 to 2.01) 1.53 (1.06 to 2.21)
 Quite a lot 122 35 (29%) 1.39 (0.94 to 2.04) 1.54 (1.05 to 2.28)
 Extremely 24 8 (33%) 1.61 (0.86 to 3.01) 1.54 (0.83 to 2.86)
Ptrend = 0.04 Ptrend = 0.03
Use of any hormonal contraceptive
 No 420 133 (32%) 1 (baseline) 1 (baseline)
 Yes 413 83 (20%) 0.63 (0.50 to 0.81) 0.66 (0.52 to 0.84)

Premenstrual symptoms were substantially less common in those women currently using hormonal contraceptives (prevalence ratio 0.63, 95% CI 0.50 to 0.81) (Table 2). Compared with those not using any form of hormonal contraception, symptoms were less common in those using noninjectable progestin-only methods, such as the progestin-only pill, the progestin implant etonogestrel, and the levonorgestrel-releasing intrauterine system (prevalence ratio 0.54, 95% CI 0.26 to 1.14), and in those using combined (estrogen-progestin) oral contraceptives (prevalence ratio 0.66, 95% CI 0.52 to 0.84). Premenstrual symptoms were not identified in any of the nine women using injectable progestins such as medroxyprogesterone acetate and norethisterone enantate with prevalence ratio 0.0 ([upper] 95% confidence point 1.11).

In a multiple regression model, use of hormonal contraceptives, perceived level of stress, and educational qualifications remained statistically significant (Table 2), but smoking, BMI, and age were no longer related to premenstrual symptoms.

In terms of alternative progestins in combined oral contraceptives, only one woman was taking drospirenone/ethinylestradiol as it was not launched in the UK until 2002 and the low estrogen-dose variant of drospirenone/ethinylestradiol is not yet in use in the UK.

Discussion

Main findings

We have shown that premenstrual symptoms occur commonly in the Southampton Women’s Survey cohort (12 - 24% of women aged 20 - 34 years) and these symptoms were linked to various lifestyle and other factors. In particular high stress, and lower educational qualifications were associated with increased prevalence of premenstrual symptoms, while the prevalence was lower in those who used hormonal contraception . Premenstrual symptoms were more common in those who were older, more obese (also reported by Strine1 and Hourani27) or who smoked tobacco (also demonstrated by Strine1 and Kritz-Silverstein28), but such associations were lost when adjusted for contraceptive usage, possibly reflecting prescribing practice, such that certain women, for example those who are obese, may be less likely to be prescribed particular contraceptives.

Comparison with other studies

The associations between premenstrual symptoms, a high perceived level of stress and a low level of educational achievement have been reported elsewhere1,27. Hourani et al27 specifically focused on job stress in military women but our more general measure of stress, similar to those used elsewhere1 identifies stress in any area of life as being associated with premenstrual symptoms. Our lack of an association between diet (measured using the ‘prudent diet score’) and premenstrual symptoms is consistent with the overall findings of the recent Study of Women’s Health Across the Nation (SWAN), a survey of 3,302 midlife US women29. This latter study found some links between certain PMS symptoms and alcohol consumption, in common with other studies1,27, though, we did not find an association between premenstrual symptoms and alcohol use in our study.

The associations we have described with hormonal contraceptives are intriguing as they are derived from a large community-based cohort. Some authors argue that contraceptives have a place in the treatment of PMS30. Notably, three recent studies reported the benefit of drospirenone-containing combined oral contraceptives in alleviating symptoms of premenstrual dysphoric disorder either on a 168 extended regime18 or cyclically with a shorter hormone-free interval than the usual seven days per cycle.19,20,30. In the case of injectable progestins it must be noted that there have been no formal controlled trials of their ability to prevent PMS. However, a recent survey of 6,026 US military women27 reported a strikingly low prevalence of premenstrual symptoms in users of injectable progestins (odds ratio 0.18, 95% CI 0.10 to 0.32), consistent with our own findings.

Strengths and weaknesses

This was a study of women from the general population, rather than those reporting to clinics or hospitals with symptoms. While diagnostic criteria have been developed for specific disorders such as premenstrual syndrome (PMS)7,8,25 and premenstrual dysphoric disorder (PMDD)24, these focus on diagnosis in a clinical setting and require diaries to be kept over a number of cycles. This is a challenge in general population research where many women do not suffer from symptoms and are less motivated to complete diaries over a long time period, thus biasing the results. We considered that six weeks was the longest time period for which we could ask women to record symptoms without severely affecting our response rate. A recent general population study over two menstrual cycles reported a similar return rate of completed diaries as in our study31. We also were unable to assess the effect of symptoms on daily living and some women may have been suffering from premenstrual symptoms that were an exacerbation of another disorder, but the diaries could not identify this robustly. Thus we do not claim to have assessed PMS according to current definitions7,8,25, and so have described the condition simply as premenstrual symptoms throughout.

We studied women from the general population and assessed associations with prevalence of the symptoms rather than the effect of therapy. Further confounders may be operating in a number of ways; for example, the need for contraception could indicate a healthier, more socially engaged population of women who are sexually active and less prone to debilitating symptoms. However, the symptoms were common in our population and although affecting quality of life for a few days each month would be unlikely to prevent the women from leading generally active lives.

Interpretation and implications

To date the therapeutic trials of hormone treatments for PMS, rather than PMDD as discussed above, have proved inconclusive14,15,32, but this may be because they assessed cyclical rather than continuous regimes. Observational evidence from our work and elsewhere18,27,30,33 suggests that hormonal contraceptive methods that suppress ovulation and act continuously may have a role in preventing premenstrual symptoms. This provides some support in favor of large well-powered randomized controlled trials of methods that induce amenorrhea in the treatment of premenstrual symptoms.

Conclusions

Premenstrual symptoms were common in this cohort of women and occurred more frequently in those with lower levels of educational attainment and in those who reported having suffered more from stress. All forms of hormonal contraception were associated with a lower prevalence of symptoms. The possible protective action of contraceptive methods that induce amenorrhea and act continuously deserve further study.

Acknowledgements

We thank the Southampton GPs who made this study possible, the Survey staff who recruited the women and collected and processed the data, and above all the women who took part in the study. The Southampton Women’s Survey was funded by the Dunhill Medical Trust, the Medical Research Council and the University of Southampton. The premenstrual symptoms sub-study reported here was funded by the Scientific Foundation Board of the Royal College of General Practitioners and the BUPA Foundation.

Footnotes

Competing interests: None declared.

Ethics Committee approval: Southampton and South West Hampshire Local Research Ethics Committee (No: 329/00).

References

  • 1.Strine TW, Chapman DP, Ahluwalia IB. Menstrual-related problems and psychological distress among women in the United States. J Women’s Health (Larchmt) 2005;14:316–23. doi: 10.1089/jwh.2005.14.316. [DOI] [PubMed] [Google Scholar]
  • 2.O’Brien PMS. The premenstrual syndrome. Br J Fam Plann. 1990;15(Suppl):13–18. [Google Scholar]
  • 3.Dean BB, Borenstein JE, Knight K, Yonkers K. Evaluating the criteria used for identification of PMS. J Women’s Health (Larchmt) 2006;15:546–555. doi: 10.1089/jwh.2006.15.546. [DOI] [PubMed] [Google Scholar]
  • 4.Mishell DR. Premenstrual disorders: epidemiology and disease burden. Am J Manag Care. 2005;11:S473–79. [PubMed] [Google Scholar]
  • 5.Halbriech U. The etiology, biology and evolving pathology of premenstrual syndromes. Psychoneurendocrinology. 2003;28:55–99. doi: 10.1016/s0306-4530(03)00097-0. [DOI] [PubMed] [Google Scholar]
  • 6.Dickerson LM, Mazyck PJ, Hunter MH. Premenstrual syndrome. Am Family Physician. 2003;67:1743–52. [PubMed] [Google Scholar]
  • 7.Halbreich U, Backstrom T, Eriksson E, et al. Clinical diagnostic criteria for premenstrual syndrome and guidelines for their quantification for research studies. Gynecological Endocrinology. 2007;23:123–130. doi: 10.1080/09513590601167969. [DOI] [PubMed] [Google Scholar]
  • 8.Royal College of Obstetricians and Gynaecologists . Management of premenstrual syndrome. Green top guideline no 48. RCOG. London: 2007. http://www.rcog.org.uk/resources/Public/pdf/green_top48_pms.pdf. [Google Scholar]
  • 9.Wyatt K, Dimmock P, Jones P, O’Brien P. Efficacy of vitamin B6 in the treatment of premenstrual syndrome: systematic review. BMJ. 1999;318:1375–81. doi: 10.1136/bmj.318.7195.1375. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Hunter MS, Ussher JM, Browne SJ, Cariss M, Jelley R, Katz M. A randomized comparison of psychological (cognitive behaviour therapy), medical (fluoxetine) and combined treatment for women with premenstrual dysphoric disorder. J Psychosom. Obstet Gynaecol. 2002;23:193–9. doi: 10.3109/01674820209074672. [DOI] [PubMed] [Google Scholar]
  • 11.Dimmock PW, Wyatt KM, Jones PW, O’Brien PMS. Efficacy of selective serotonin-reuptake inhibitors in premenstrual syndrome: a systematic review. Lancet. 2004;13:812–21. doi: 10.1016/s0140-6736(00)02754-9. [DOI] [PubMed] [Google Scholar]
  • 12.Freeman E, Rickels K, Arredondo F, Kao LC, Pollack S, Sondheimer S. Full or half cycle treatment of severe premenstrual syndrome with a serotonergic antidepressant. J Clin Psychopharmacol. 1999;19:3–8. doi: 10.1097/00004714-199902000-00002. [DOI] [PubMed] [Google Scholar]
  • 13.Dalton K. The Premenstrual Syndrome and Progesterone Therapy. 2nd ed. Year Book Medical Publisher; Chicago Il: 1984. [Google Scholar]
  • 14.Wyatt K, Dimmock P, Jones P, Obhrai M, O’Brien S. Efficacy of progesterone and progestogens in management of premenstrual syndrome: a systematic review. BMJ. 2001;323:1–8. doi: 10.1136/bmj.323.7316.776. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Ford O, Lethaby A, Mol B, Roberts H. Progesterone for premenstrual syndrome. Cochrane Database of Systematic Reviews. 2006;(4) doi: 10.1002/14651858.CD003415.pub2. Art. No.: CD003415. DOI: 10.1002/14651858.CD003415.pub2. [DOI] [PubMed] [Google Scholar]
  • 16.Watson NR, Studd JW, Savvas M, Garnett T, Baber RJ. Treatment of severe premenstrual syndrome with oestradiol patches and cyclical oral norethisterone. Lancet. 1989;ii:730–2. doi: 10.1016/s0140-6736(89)90784-8. [DOI] [PubMed] [Google Scholar]
  • 17.Magos AL, Brincat M, Studd JW. Treatment of the premenstrual syndrome by subcutaneous estradiol implants and cyclical oral norethisterone: placebo controlled study. Br Med J. 1986;292:1629–33. doi: 10.1136/bmj.292.6536.1629. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Coffee A, Kuehl T, Willis S, Sulak P. Oral contraceptives and premenstrual symptoms: Comparison of a 21/7 and extended regime. Amer J Obs Gyn. 2006;195:1311–9. doi: 10.1016/j.ajog.2006.05.012. [DOI] [PubMed] [Google Scholar]
  • 19.Pearlstein T, Bachmann G, Zacur H, Yonkers K. Treatment of premenstrual dysphoric disorder with a new drospirenone-containing oral contraceptive formulation. Contraception. 2005;72:414–421. doi: 10.1016/j.contraception.2005.08.021. [DOI] [PubMed] [Google Scholar]
  • 20.Yonkers K, Brown C, Pearlstein, Foegh M, Sampso-Landers C, Rapkin A. Efficacy of a new low-dose oral contracetive with drospirenone in premenstrual dysphoric disorder. Obstet Gynecol. 2005;106:492–501. doi: 10.1097/01.AOG.0000175834.77215.2e. [DOI] [PubMed] [Google Scholar]
  • 21.Inskip HM, Godfrey KM, Robinson SM, et al. Cohort profile: The Southampton Women’s Survey. Int J Epidemiol. 2006;35:42–48. doi: 10.1093/ije/dyi202. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Moos RH, Kopell BS, Melges FT, et al. Fluctuations in symptoms and moods during the menstrual cycle. J Psychosom Res. 1969;13:37–44. doi: 10.1016/0022-3999(69)90017-8. [DOI] [PubMed] [Google Scholar]
  • 23.Robinson S, Crozier S, Borland S, Hammond J, Barker D, Inskip H. The impact of educational attainment on the quality of young women’s diets. Eur J Clin Nutr. 2004;58:1174–80. doi: 10.1038/sj.ejcn.1601946. [DOI] [PubMed] [Google Scholar]
  • 24.American Psychiatric Association . Diagnostic and Statistical Manual of Mental Disorders. 4th edn. American Psychiatric Association Inc; Washington: 1994. pp. 715–718. [Google Scholar]
  • 25.American College of Obstetricians and Gynecologists . Premenstrual Syndrome. American College of Obstetricians and Gynecologists; Washington, DC: 2000. ACOG Practice Bulletin No. 15. [Google Scholar]
  • 26.Barros AJD, Hirakata VN. Alternatives for logistic regression in cross-sectional studies: an empirical comparison of models that directly estimate the prevalence ratio. BMC Med Res Methodol. 2003;3:21. doi: 10.1186/1471-2288-3-21. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Hourani L, Yuan, Bray RM. Psychosocial and lifestyle correclates of premenstrual symptoms among military women. J Women’s Health (Larchmt) 2004;13:812–821. doi: 10.1089/jwh.2004.13.812. [DOI] [PubMed] [Google Scholar]
  • 28.Kritz-Silverstein D, Wingard D, Garland F. The association of behaviour and lifestyle factors with menstrual symptoms. J Womens Health Gend Based Med. 1999;8:1185–93. doi: 10.1089/jwh.1.1999.8.1185. [DOI] [PubMed] [Google Scholar]
  • 29.Gold EB, Bair Y, Block G, et al. Diet and lifestyle factors associated with premenstrual symptoms in a racially diverse community sample: Study of Women’s Health Across the Nation (SWAN) J Women’s Health (Larchmt) 2007;16:641–56. doi: 10.1089/jwh.2006.0202. [DOI] [PubMed] [Google Scholar]
  • 30.Sulak PJ. Ovulation suppression of premenstrual symptoms using oral contraceptives. Am J Managed Care. 2005;11:S492–497. [PubMed] [Google Scholar]
  • 31.Borenstein JE, Dean BB, Yonkers KA, Endicott J. Using the Daily Record of Severity of Problems as a Screening Instrument for Premenstrual Syndrome. Obst Gynecol. 2007;5:1068–75. doi: 10.1097/01.AOG.0000259920.73000.3b. [DOI] [PubMed] [Google Scholar]
  • 32.Bancroft J, Rennie D. The impact of oral contraceptives on the experience of perimenstrual mood, clumsiness, food craving and other symptoms. J Psychosom Res. 1993;37:195–202. doi: 10.1016/0022-3999(93)90086-u. [DOI] [PubMed] [Google Scholar]
  • 33.Sulak PJ, Kuehl TJ, Coffee A, Willis S. Prospective analysis of occurrence and management of breakthrough bleeding during an oral contraceptive regime. Am J Obstet Gynecol. 2006;195:935–41. doi: 10.1016/j.ajog.2006.02.048. [DOI] [PubMed] [Google Scholar]

RESOURCES