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East Asian Arch Psychiatry 2014;24:174-7 Commentary

Premenstrual Dysphoric Disorder in the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition: Contributions from Asia DSM-5診斷的經前煩燥症:亞洲研究現況

N Mehta, S Mehta

Abstract

Premenstrual dysphoric disorder has been included as a separate diagnostic entity in the chapter of ‘Depressive Disorders’ of the Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM- 5). The antecedent, concurrent, and predictive diagnostic validators of premenstrual dysphoric disorder have been reviewed by a sub-workgroup of the DSM-5 Mood Disorders Work Group, which includes a panel of experts on women’s mental health. Contributions from the Asian continent have been mainly in the form of prevalence studies. Genetic and neurobiological domains of premenstrual dysphoric disorder largely remain untouched in Asia and offer a potential area for investigation.

Key words: Asia; Diagnostic and Statistical Manual of Mental Disorders;

摘要

經前煩躁症已被精神疾病診斷及統計手冊第五版(DSM-5)列為屬抑鬱症的單獨診斷實體,而 DSM-5情緒障礙工作小組旗下的女性心理健康專家子工作組也根據前期、現行和預測驗證因子 為此症作審查。有關此症的亞洲文獻以現患率研究為主,而涉及基因和神經生物學這些值得研 究的領域則很少。

關鍵詞:亞洲、精神疾病診斷及統計手冊、經前綜合徵

Dr Nidhi Mehta, DGO, Department of Obstetrics and Gynaecology, Bangalore symptoms must be present in the final week before Medical College and Research Institute, Bengaluru, Karnataka 560002, . Dr Shubham Mehta, MD, Department of Psychiatry, SMS Medical College, the onset of menses, start to improve within a few Jaipur, Rajasthan 302004, India. days after the onset of menses, and become minimal or absent in the week post-menses. Address for correspondence: Dr Shubham Mehta, Room No. 9, N. M. H. P. Trainees Hostel, Psychiatric Centre Campus, Sethi Colony, Jaipur, Rajasthan (B) One (or more) of the following symptoms must be 302004, India. present: Tel: (91) 9799723735; email: [email protected] • Marked affective lability (eg mood swings, feeling Submitted: 20 November 2013; Accepted: 27 January 2014 suddenly sad or tearful, or increased sensitivity to rejection). • Marked irritability or anger or increased interpersonal conflicts. Introduction • Markedly depressed mood, feelings of hopelessness, or self-deprecating thoughts. Among all the changes and new inclusions made in the • Marked anxiety, tension, and / or feelings of being Diagnostic and Statistical Manual of Mental Disorders, 5th keyed up or on the edge. edition (DSM-5),1 one significant change has been moving (C) One (or more) of the following symptoms must be the premenstrual dysphoric disorder (PMDD) from the additionally present, to reach a total of 5 symptoms DSM-IV Appendix-B, “Criteria Sets and Axes Provided when combined with symptoms from criterion B for Further Study”2 to the main body of DSM-5. This entity above: now has its own 7 diagnostic criteria as described below1: • Decreased interest in usual activities (eg work, (A) In the majority of menstrual cycles, at least 5 school, friends, and hobbies).

174 © 2014 Hong Kong College of Psychiatrists Premenstrual Dysphoric Disorder

• Subjective difficulty in concentration. different measures used by various researchers to assess • Lethargy, easy fatigability, or marked lack of its symptomatology. In a study of 136 patients attending a energy. specialised mental health clinic in gynaecology settings in • Marked change in appetite, overeating, or specific Taiwan, the incidence of DSM-IV PMDD criteria was noted food cravings. to be as high as 16.3%.6 • Hypersomnia or insomnia. The same study6 also examined the individual • A sense of being overwhelmed or out of control. characteristics of women with PMDD. It was found that • Physical symptoms such as breast tenderness 86% of the women had another concurrent psychiatric or swelling, joint or muscle pain, sensation of disorder. In another study that examined the personality of “bloating,” or weight gain (the symptoms in Criteria 142 patients, the investigators found a significant overlap A to C must have been met for most menstrual in overall personality profiles of women with PMDD and cycles that occurred in the preceding year). major depressive disorder (MDD).7 Impulsiveness subscore (D) The symptoms are associated with clinically was significantly higher in women with PMDD versus those significant distress or interference with work, school, with MDD. usual social activities, or relationships with others (eg The possible relationship between environmental avoidance of social activities; decreased productivity factors such as stress and seasonal changes and the onset and efficiency at work, school, or home). or expression of PMDD symptoms, as well as the role of (E) The disturbance is not merely an exacerbation of interpersonal trauma has been investigated in the West8 but the symptoms of another disorder, such as major not in the Asian continent. Also, there is a lack of family depressive disorder, panic disorder, persistent studies from Asia highlighting the role of genetics in the depressive disorder (dysthymia), or a personality aetiogenesis of PMDD as against a longitudinal population- disorder (although it may co-occur with any of these based twin study from the West9 which reported the disorders). heritability of premenstrual symptoms. (F) Criterion A should be confirmed by prospective daily ratings during at least 2 symptomatic cycles. Concurrent Validators (G) The symptoms are not attributable to the physiological Concurrent or biological validators include effects of a substance (eg a drug of abuse, a medication, neuropsychological, neurophysiological, and neuroimaging other treatment) or another medical condition (eg factors. The Asian literature has examined the physiological hyperthyroidism). differences present in PMDD relative to controls. One This move is significant as it reflects international study examined serotonergic functioning in 24 Japanese concerns about betterment of women’s mental health. women who had PMDD, premenstrual symptoms (PMS) or The special panel of experts on women’s mental were healthy (controls), and found significant differences health created by the Mood Disorders Work Group for across these 3 groups as measured by adrenocorticotropic DSM-5 found robust evidence regarding the distinctiveness hormone and cortisol responses to challenge.10 of PMDD. The reproductive mood disorder specialists have Subjects with PMDD showed higher serotonergic function thoroughly analysed the diagnostic validators of PMDD in the follicular phase but lower serotonergic function from the literature and recommended PMDD to reside in the luteal phase compared with women in the other 2 as a diagnosis in a newly created chapter of ‘Depressive groups. Matsumoto et al11 examined autonomic function, Disorders’ in DSM-5. as measured by heart-rate variability (HRV) in Japanese We view this move with interest and try to generate a women diagnosed with PMDD or PMS or who were healthy gestalt of research findings regarding PMDD from the Asian (controls). They found that women in the PMDD group had continent. To consider any disorder as a valid diagnostic the greatest decrease in HRV among the 3 groups. entity, it must have separate antecedent, concurrent / Studies from the West12-14 have suggested that biological, and predictive diagnostic validators.3 While we symptom severity in PMDD is correlated with levels scrolled through the literature, we found that there have of oestradiol, , or neurosteroids such as been quite a few contributions from Asia when analysed in and sulfate. However, terms of diagnostic validators of PMDD. With the help of we could not find any neuroimaging studies pertaining this article, we intend to provide a gist of these contributions to PMDD, or studies assessing the neuropsychological as this would help in identifying the strengths and lacunas correlates of PMDD in the Asian population. However, even in the Asian literature on PMDD, thus, providing a probable in the West, such studies remain in a stage of infancy and direction for further research in this area. only a few studies have reported specific central nervous system differences in neural network activation, Antecedent Validators metabolism, and neurotransmitter concentration between These include demographic factors, pre-morbid personality women with PMDD and healthy comparison subjects, based traits, family studies, and environmental risk factors or on findings of functional magnetic resonance imaging,15 precipitating factors. The prevalence of PMDD in Asian positron emission tomography,16 and proton magnetic studies ranged from 1.2%4 to 6.4%,5 keeping in mind the resonance spectroscopy,17 respectively.

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Predictive Validators Declaration These include course and outcome of disorder and the response to treatment. Assessment of stability of symptom The authors declared no conflict of interest in this study. pattern prospectively, from cycle to cycle, would serve as a guide to establish diagnostic stability and also the course References of PMDD. Furthermore, longitudinal studies are imperative 1. American Psychiatric Association. Diagnostic and Statistical Manual to determine the outcome of PMDD and its response to of Mental Disorders, 5th edition. Washington, DC: American treatment. Psychiatric Association; 2013. There have been some follow-up studies assessing 2. American Psychiatric Association. Diagnostic and Statistical Manual 18 of Mental Disorders, 4th edition. Washington, DC: American treatment response in PMDD. Hsiao and Liu conducted Psychiatric Association; 1994. an open-label study to examine the response of 30 patients 3. Robins E, Guze SB. Establishment of diagnostic validity in psychiatric with PMDD to and found significant reduction illness: its application to . Am J Psychiatry 1970;126:107- in mood and behaviour subscales of Prospective Record 11. of the Impact and Severity of Menstrual symptomatology 4. Takeda T, Tasaka K, Sakata M, Murata Y. Prevalence of premenstrual syndrome and premenstrual dysphoric disorder in Japanese women. calendar, the Zung Self-Rating Scale (Zung- Arch Womens Ment Health 2006;9:209-12. SDS), Hamilton Anxiety Rating Scale, and Hamilton 5. Banerjee N, Roy K, Takkar D. Premenstrual dysphoric disorder: a Depression Rating Scale (HDRS). Wu et al19 examined study from India. Int J Fertil Womens Med 2000;45:342-4. the effect of paroxetine when administered intermittently 6. Hsiao MC, Liu CY, Chen KC, Hsieh TT. Characteristics of women versus continuously in 36 women seeking treatment for using a mental health clinic in a gynecologic out-patient setting. Psychiatry Clin Neurosci 2002;56:459-63. PMDD. They followed the patients for 6 menstrual cycles 7. Hsu SC, Liu CY, Hsiao MC. A comparison of the Tridimensional and found that rate of response on HDRS, Zung-SDS, Personality Questionnaire in premenstrual dysphoric disorder and and Clinical Global Impression scale ranged from 50% to major depressive disorder. Compr Psychiatry 2007;48:366-70. 78.6% with continuous dosing and from 37.5% to 93.8% 8. Fontana AM, Palfai TG. Psychosocial factors in premenstrual with intermittent dosing, with no significant differences dysphoria: stressors, appraisal, and coping processes. J Psychosom Res 1994;38:557-67. between the 2 treatment protocols. 9. Kendler KS, Karkowski LM, Corey LA, Neale MC. Longitudinal Similarly, the western literature mentions a preferential population-based twin study of retrospectively reported premenstrual response of PMDD patients to reuptake inhibitors symptoms and lifetime major depression. Am J Psychiatry as compared with other mood disorders.20 Likewise, PMDD 1998;155:1234-40. has been shown to be responsive to treatment with oral 10. Inoue Y, Terao T, Iwata N, Okamoto K, Kojima H, Okamoto T, et al. 21,22 Fluctuating serotonergic function in premenstrual dysphoric disorder contraceptives containing progestin drospirenone as and premenstrual syndrome: findings from neuroendocrine challenge well as to ovarian suppression with gonadotropin-releasing test. (Berl) 2007;190:213-9. hormone analogue agonists.23,24 11. Matsumoto T, Ushiroyama T, Kimura T, Hayashi T, Moritani T. Roles of non-pharmacological treatments like herbal Altered autonomic nervous system activity as a potential etiological medications,25 St. John’s wort,26 and acupuncture27 have factor of premenstrual syndrome and premenstrual dysphoric disorder. Biopsychosoc Med 2007;1:24. been examined to a larger extent in Asian studies than in 12. Wang M, Seippel L, Purdy RH, Bäckström T. Relationship between western studies. These treatment modalities have been symptom severity and steroid variation in women with premenstrual proven beneficial in improving both emotional and physical syndrome: study on serum pregnenolone, , 5 symptoms associated with PMDD. alpha-pregnane-3,20-dione and 3 alpha-hydroxy-5 alpha-pregnan-20- However, the treatment-seeking females are quite few one. J Clin Endocrinol Metab 1996;81:1076-82. 13. Rapkin AJ, Morgan M, Goldman L, Brann DW, Simone D, Mahesh as they are unaware of the terminology of PMS / PMDD, VB. Progesterone metabolite allopregnanolone in women with 28 as reported recently. This highlights the underlying need premenstrual syndrome. Obstet Gynecol 1997;90:709-14. of educating women about PMDD, and also creating 14. Seippel L, Bäckström T. Luteal-phase relates to symptom awareness about the available treatment options. severity in patients with premenstrual syndrome. J Clin Endocrinol Metab 1998;83:1988-92. 15. Protopopescu X, Tuescher O, Pan H, Epstein J, Root J, Chang L, et Conclusion al. Toward a functional neuroanatomy of premenstrual dysphoric disorder. J Affect Disord 2008;108:87-94. It appears that the Asian literature has contributed primarily 16. Rapkin AJ, Berman SM, Mandelkern MA, Silverman DH, Morgan in the form of prevalence studies on PMDD. There are some M, London ED. Neuroimaging evidence of cerebellar involvement in premenstrual dysphoric disorder. Biol Psychiatry 2011;69:374-80. studies regarding the physiological correlates of PMDD 17. Epperson CN, Haga K, Mason GF, Sellers E, Gueorguieva R, Zhang and some have prospectively assessed treatment responses W, et al. Cortical gamma-aminobutyric acid levels across the menstrual in such patients. Environmental and genetic risk factors cycle in healthy women and those with premenstrual dysphoric and neuropsychological and neuroanatomical correlates disorder: a proton magnetic resonance spectroscopy study. Arch Gen of PMDD are domains which remain largely untouched Psychiatry 2002;59:851-8. 18. Hsiao MC, Liu CY. Effective open-label treatment of premenstrual in Asia. On a positive note, this offers enormous scope for dysphoric disorder with venlafaxine. Psychiatry Clin Neurosci Asian investigators to widely explore these areas and, thus, 2003;57:317-21. contribute to improvement in women’s mental health. 19. Wu KY, Liu CY, Hsiao MC. Six-month paroxetine treatment of

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premenstrual dysphoric disorder: continuous versus intermittent 24. Schmidt PJ, Nieman LK, Danaceau MA, Adams LF, Rubinow DR. treatment protocols. Psychiatry Clin Neurosci 2008;62:109-14. Differential behavioral effects of gonadal steroids in women with and 20. Dimmock PW, Wyatt KM, Jones PW, O’Brien PM. Efficacy of in those without premenstrual syndrome. N Engl J Med 1998;338:209- selective serotonin-reuptake inhibitors in premenstrual syndrome: a 16. systematic review. Lancet 2000;356:1131-6. 25. Yamada K, Kanba S. Effectiveness of kamishoyosan for premenstrual 21. Pearlstein TB, Bachmann GA, Zacur HA, Yonkers KA. Treatment of dysphoric disorder: open-labeled pilot study. Psychiatry Clin Neurosci premenstrual dysphoric disorder with a new drospirenone containing 2007;61:323-5. oral contraceptive formulation. Contraception 2005;72:414-21. 26. Huang KL, Tsai SJ. St. John’s Wort ( Perforatum) as 22. Yonkers KA, Foegh ML. A new low-dose, drospirenone-containing treatment for premenstrual dysphoric disorder: case report. Int J oral contraceptive (OC) with a new dosing regimen is effective in Psychiatry Med 2003;33:295-7. reducing premenstrual dysphoric disorder (PMDD). Fertil Steril 27. Taguchi R, Matsubara S, Yoshimoto S, Imai K, Ohkuchi A, Kitakoji 2004;82(Suppl 2):S102-3. H. Acupuncture for premenstrual dysphoric disorder. Arch Gynecol 23. Wyatt KM, Dimmock PW, Ismail KM, Jones PW, O’Brien PM. The Obstet 2009;270:877-81. effectiveness of GnRHa with and without “add-back” therapy in 28. Choi D, Lee DY, Lehert P, Lee IS, Kim SH, Dennerstein L. The impact treating premenstrual syndrome: a meta-analysis. BJOG 2004;111:585- of premenstrual symptoms on activities of daily life in Korean women. 93. J Psychosom Obstet Gynaecol 2010;31:10-5.

Acknowledgements

The Editorial Board of East Asian Archives of Psychiatry wishes to thank the reviewers for volunteering their expertise and insight, and for their hard work and diligence in reviewing articles for the year 2014.

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