Abstract
We aimed to investigate whether females with psychosexual disorders were associated with the risk of affective and other psychiatric disorders. A total of 2240 enrolled individuals, with 560 patients with psychosexual disorders and 1680 subjects without psychosexual disorders (1:3) matched for age and index year, from the Longitudinal Health Insurance Database, retrieved from the National Health Insurance Research Database (NHIRD), between 2000 and 2015 in Taiwan. The multivariate Cox regression model was used to compare the risk of developing psychiatric disorders during the 15 years of follow-up. There were 98 in the cohort with psychosexual disorders (736.07 per 100,000 person-year) and 119 in the non-cohort without psychosexual disorders (736.07 per 100,000 person-year) that developed psychiatric disorders. The multivariate Cox regression model revealed that the adjusted hazard ratio (HR) was 9.848 (95% CI = 7.298 — 13.291, p < 0.001), after the adjustment of age, monthly income, urbanization level, geographic region, and comorbidities. Female patients with psychosexual disorders were associated with the risk of psychiatric disorders. This finding could be a reminder for clinicians about the mental health problems in patients with psychosexual disorders.
Supplementary Information
The online version contains supplementary material available at 10.1186/s12888-021-03060-1.
Keywords: Psychosexual disorders, Affective disorders, Females, National Health Insurance Research Database, Cohort study
Background
Psychosexual disorders could be classified into sexual dysfunctions, paraphilias, and gender identity disorders [1, 2], and these psychosexual disorders are regarded as part of the psychiatric disorders [3]. Previous studies have shown that female patients with psychosexual disorders, such as sexual dysfunctions, paraphilias, and gender identity disorders, would suffer from emotional distress, social embarrassment, and even stigmatization [4, 5].
Several researchers have shown the neurodevelopmental interlinks between the psychosexual and psychiatric disorders: Sex differences in the microglial function might partially explain the differences observed in susceptibilities and outcomes of the neuropsychiatric disorders in men and women [6]. Rajkumar (2014) pointed out that both gender identity disorders and schizophrenia are associated with altered cerebral sexual dimorphism and changes in cerebral lateralization [7]. Previous studies have also found that endocrine factors are related to female psychosexual disorders. For example, sex steroids, such as estrogen or progestin, insufficiency may adversely affect central sexual thought processes, and contribute to the female sexual dysfunctions, such as hypoactive sexual desire disorder [8]. Also, gender dysphoria may have several genes involved in the sex hormone–signaling in the brains [9]. Sex hormones such as estrogen have many effects on anxiety and depression [10]. Several studies have found mutual relations between psychiatric comorbidity and psychosexual disorders [11–16]. For the clinicians, it is essential to better understand the mutual relationship between female patients with psychosexual disorders and their psychiatric morbidity. And these psychiatric disorders might well contribute to the distress, disability, or an increased risk of suffering death, pain, or disability, and consequent behavioral, psychological, or biological dysfunctions [3, 17]. Therefore, several neurodevelopmental, endocrine and psychological factors could be the linkage between psychosexual and psychiatric disorders.
Previous studies have found that depressive disorders are frequently associated with sexual dysfunction, across all the phases of sexual responses [18], and the attention problems related to anxiety might impair sexual motivation even with adequate stimuli [19]. Besides, sexual dysfunction is frequent in patients with posttraumatic stress disorder [20, 21]. However, some researchers have revealed that no psychiatric comorbidity was found in female patients with gender identity disorder [22, 23]. Furthermore, the relationship between female paraphilia and psychiatric disorders remains unclear, since patients with female paraphilia are rare [24, 25]. Therefore, depression, anxiety, and trauma-related disorders are associated with sexual dysfunctions, and also with the association between psychiatric disorders and paraphilia and gender identity disorder. Besides, there is a gap in the literature that no previous cohort studies have been conducted to examine the risk of psychiatric disorders in female patients with psychosexual disorders. We hypothesize that these psychosexual disorders are associated with the risk of psychiatric disorders in a long-term follow-up. We, therefore, conduct the present study, using Taiwan’s National Health Insurance Research Database (NHIRD), to investigate the association between psychosexual disorders and psychiatric disorders, in a 15-year follow-up.
Methods
Data sources
The National Health Insurance (NHI) Program was launched in Taiwan in 1995, and as of June 2009, including contracts with 97% of the medical providers, with approximately 23 million beneficiaries, or more than 99% of the entire population [26]. The National Health Insurance Research Database (NHIRD) uses the International Classification of Diseases, 9th Revision, Clinical Modification (ICD-9-CM) codes to record the diagnoses [27]. The present study has used the NHIRD to identify the inpatients with a discharge diagnosis of psychosexual disorders based on the ICD-9-CM codes, including sexual dysfunctions, paraphilia, and gender identity disorders, during 2000–2015. The paraphilias included the diagnoses as exhibitionism, fetishism, frotteurism, pedophilia, sexual masochism, sexual sadism, transvestic fetishism, voyeurism, other paraphilia, and paraphilia, not otherwise specified [3]. All the ICD-9-CM codes of psychosexual disorders are as listed in Table S1. In this database, all the personal identification data were enciphered, for the protection of the privacy of the patients. The records of ambulatory care visits and inpatient claims periodically were reviewed randomly by the NHI Administration to verify the accuracy of the diagnoses [28]. Several previous studies have documented the details of the program [29–33].
Study design and sampled participants
Patients with newly diagnosed psychosexual disorders were selected from the 2 million Longitudinal Health Insurance Database (LHID), randomized retrieved from the NHIRD, which covers 99% of the entire population of Taiwan, between January 1, 2000, and December 31, 2015. The patients with psychosexual disorders before 2000 were excluded. Besides, the patients diagnosed with psychiatric disorders before 2000, or before their first visit for any psychosexual disorder, were also excluded. In Taiwan, the legal age of full civil competency is 20 years of age, according to Taiwan’s Civil Code [34], therefore, all patients aged < 20, were excluded as well. In this study, 560 patients with the psychosexual disorder and 1680 subjects without psychosexual disorders, were 1:3 matched, for age and index-year control, with a statistic power of 0.72 [35], and little power improvement resulted from increasing the number of controls while the ratio beyond 1:3 or 1:4 [36]. Therefore, the present study is a population-based, matched cohort study.
Covariates
The covariates included age groups (20–49, ≥ 50 years), geographical area of residence (north, center, south, and east of Taiwan), urbanization level of residence (levels 1 to 4), and monthly income (in New Taiwan Dollars [NT$]; < 18,000, 18,000-34,999, ≥35,000). The urbanization level of residence was defined according to the population and various indicators of the level of development. Level 1 was defined as a population of > 1,250,000, and a specific designation as political, economic, cultural, and metropolitan development. Level 2 was defined as a population between 500,000 and 1,249,999, and as playing an important role in the politics, economy, and culture. Urbanization levels 3 and 4 were defined as a population between 149,999 and 499,999, and < 149,999, respectively.
Comorbidity
We assessed the comorbidities by using the Charlson Comorbidity Index (CCI), which categorizes comorbidities using the ICD-9-CM codes, and scores each comorbidity category [37–39]. The CCI is used for comorbidity adjustment as a useful measure and substitutes for the usage of the individual comorbidity variables in health services research [40]. In CCI, the comorbidities include myocardial infarction, congestive heart failure, peripheral vascular disease, cerebrovascular disease, chronic obstructive pulmonary disease, dementia, paralysis, diabetes mellitus, diabetes with sequelae, chronic renal failure, cirrhosis of the liver, moderate-severe liver disease, peptic ulcers, rheumatoid arthritis, and AIDS [41]. The combination of all the scores was regarded as a single comorbidity score. A score of zero indicates that no comorbidities were found, and higher scores indicate higher comorbidity burdens [42].
Outcome measures
Enrolled individuals in these two cohorts were tracked for 15 years, starting from the index date, to identify those who developed psychiatric disorders, comprising dementia, anxiety disorders, depressive disorders, bipolar disorders, eating disorders, sleep disorders, and psychotic disorders, withdrew from the NHI program, or reached the end of 2015. All the ICD-9-CM codes of psychiatric disorders are as listed in Table S1.
Statistical analysis
All statistical analyses were performed using the SPSS for Windows, version 22.0 (IBM Corp., Armonk, NY). χ2 and t-tests were used to appraise the distributions of the categorical and continuous variables, respectively. The multivariate regression model was used to determine the risk of psychiatric disorders since death can act as a competing risk factor for psychiatric disorders [43, 44]. The results were presented as a hazard ratio (HR) with a 95% confidence interval (CI). Differences in the risk of psychiatric disorders between the study and control groups were estimated using the Kaplan-Meier method with the log-rank test. A 2-tailed p-value < 0.001 was considered to indicate a statistical significance, to minimize the type I error as possible.
Results
Sample characteristics
There was no significant difference between these two cohorts in age, marital status, education, insured monthly premiums, and the CCI scores. The cohort with psychosexual disorders tended to search for medical help in summer, autumn, and winter. Furthermore, the cohort with psychosexual disorders tended to live in the north, and the offshore islands resided more in the region of urbanization level 2 and received their medical treatments in the medical centers (Table 1).
Table 1.
Characteristics of study at the baseline
| Psychosexual disorders | Total | With | Without | P | |||
|---|---|---|---|---|---|---|---|
| Variables | n | % | n | % | n | % | |
| Total | 2240 | 560 | 25.00 | 1680 | 75.00 | ||
| Age (years) | 35.08 ± 12.99 | 34.70 ± 11.46 | 35.21 ± 13.46 | 0.421 | |||
| Age group (years) | 0.999 | ||||||
| 20–49 | 2016 | 90.00 | 504 | 90.00 | 1512 | 90.00 | |
| ≧50 | 224 | 10.00 | 56 | 10.00 | 168 | 10.00 | |
| Married | 0.692 | ||||||
| Yes | 936 | 41.79 | 230 | 41.07 | 706 | 42.02 | |
| No | 1304 | 58.21 | 330 | 58.93 | 974 | 57.98 | |
| Education (years) | 0.823 | ||||||
| < 12 | 568 | 25.36 | 144 | 25.71 | 424 | 25.24 | |
| ≧12 | 1672 | 74.64 | 416 | 74.29 | 1256 | 74.76 | |
| Insured premium (NT$) | 0.663 | ||||||
| < 18,000 | 1974 | 88.13 | 499 | 89.11 | 1475 | 87.80 | |
| 18,000-34,999 | 184 | 8.21 | 41 | 7.32 | 143 | 8.51 | |
| ≧35,000 | 82 | 3.66 | 20 | 3.57 | 62 | 3.69 | |
| CCI_R | 0.39 ± 1.37 | 0.30 ± 0.94 | 0.42 ± 1.48 | 0.081 | |||
| Season | < 0.001 | ||||||
| Spring (March–May) | 581 | 25.94 | 91 | 16.25 | 490 | 29.17 | |
| Summer (June–August) | 602 | 26.88 | 154 | 27.50 | 448 | 26.67 | |
| Autumn (September–November) | 476 | 21.25 | 147 | 26.25 | 329 | 19.58 | |
| Winter (December-Februrary) | 581 | 25.94 | 168 | 30.00 | 413 | 24.58 | |
| Location | < 0.001 | ||||||
| Northern Taiwan | 945 | 42.19 | 308 | 55.00 | 637 | 37.92 | |
| Middle Taiwan | 581 | 25.94 | 112 | 20.00 | 469 | 27.92 | |
| Southern Taiwan | 574 | 25.63 | 112 | 20.00 | 462 | 27.50 | |
| Eastern Taiwan | 126 | 5.63 | 21 | 3.75 | 105 | 6.25 | |
| Outlets islands | 14 | 0.63 | 7 | 1.25 | 7 | 0.42 | |
| Urbanization level | < 0.001 | ||||||
| 1 (The highest) | 784 | 35.00 | 126 | 22.50 | 658 | 39.17 | |
| 2 | 1029 | 45.94 | 357 | 63.75 | 672 | 40.00 | |
| 3 | 112 | 5.00 | 21 | 3.75 | 91 | 5.42 | |
| 4 (The lowest) | 315 | 14.06 | 56 | 10.00 | 259 | 15.42 | |
| Level of care | < 0.001 | ||||||
| Medical center | 798 | 35.63 | 357 | 63.75 | 441 | 26.25 | |
| Regional hospital | 595 | 26.56 | 147 | 26.25 | 448 | 26.67 | |
| Local hospital | 847 | 37.81 | 56 | 10.00 | 791 | 47.08 | |
P: Chi-square / Fisher exact test on category variables and t-test on continue variables
Without married: un-married, divorce, spouse death, and unknown
Education years < 12: elementary school, junior high school, (vocational) high school, and unknown; Education years ≧12: university, college, and graduate
CCI_R Charlson comorbidity index removed dementia
The cumulative incidence of psychiatric disorders
There were 98 in the cohort with psychosexual disorders and 119 in the comparison cohort that developed psychiatric disorders (3444.66 vs 736.07 per 100,000 person-year). Figure 1 depicts that the difference was statistically significant in the Kaplan-Meier survival analysis (log-rank, p < 0.001).
Fig. 1.

Kaplan-Meier for the cumulative incidence of psychiatric disorders aged 20 and over stratified by psychosexual disorders with the log-rank test
Changes of psychosexual disorders in the follow-up period, 2000–2015
Figure 2 reveals that there was no significant difference between the beginning and the end-point of the follow-up in all these psychosexual disorders, between 2000 and 2015. Besides, the treatment prevalence of the female psychosexual disorders was 0.007% of the sexual dysfunctions, paraphilias were around 0.004%, and the female-to-male (FTM) gender identity disorder was 0.017%, during the 15-year follow-up.
Fig. 2.
Rate and subgroup proportions of psychosexual disorders in the study period
HR analysis of psychiatric disorders in patients with psychosexual disorders
The multivariate Cox regression model showed that the adjusted HR of the psychosexual disorders cohort in the development of psychiatric disorders was 9.848 (95% CI = 7.298—13.291, p < 0.001), after adjustment for age, marital status, education, comorbidity (CCI scores), urbanizations/areas of residence, insurance premiums, seasons of visits, and levels of medical facilities, as compared to the control group (Table 2).
Table 2.
Factors of psychiatric disorders stratified by variables listed in the table by using the Cox regression model
| Psychosexual disorders (With vs. Without) | With | Without | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Stratified | Event | PYs | Rate (per 105 PYs) | Event | PYs | Rate (per 105 PYs) | Adjusted HR | 95% CI | 95% CI | P |
| Total | 98 | 2844.99 | 3444.66 | 119 | 16,167.03 | 736.07 | 9.848 | 7.298 | 13.291 | < 0.001 |
| Age group (years) | ||||||||||
| 20–49 | 70 | 1823.05 | 3839.71 | 91 | 9797.14 | 928.84 | 8.699 | 6.447 | 11.740 | < 0.001 |
| ≧50 | 28 | 1021.93 | 2739.91 | 28 | 6369.89 | 439.57 | 13.117 | 9.720 | 17.703 | < 0.001 |
| Married | ||||||||||
| Yes | 38 | 1400.98 | 2712.38 | 48 | 7754.07 | 619.03 | 9.221 | 6.833 | 12.444 | < 0.001 |
| No | 60 | 1444.00 | 4155.12 | 71 | 8412.96 | 843.94 | 10.361 | 7.678 | 13.983 | < 0.001 |
| Education (years) | ||||||||||
| < 12 | 27 | 1034.02 | 2611.17 | 20 | 8026.18 | 249.18 | 22.051 | 16.341 | 29.761 | < 0.001 |
| ≧12 | 71 | 1810.97 | 3920.56 | 99 | 8140.85 | 1216.09 | 6.784 | 5.028 | 9.156 | < 0.001 |
| Insured premium (NT$) | ||||||||||
| < 18,000 | 67 | 1512.44 | 4429.93 | 73 | 7558.18 | 965.84 | 9.652 | 7.153 | 13.026 | < 0.001 |
| 18,000-34,999 | 24 | 851.67 | 2818.01 | 38 | 4311.00 | 881.47 | 6.728 | 4.986 | 9.080 | < 0.001 |
| ≧35,000 | 7 | 480.88 | 1455.66 | 8 | 4297.85 | 186.14 | 16.457 | 12.195 | 22.210 | < 0.001 |
| Season | ||||||||||
| Spring | 21 | 535.28 | 3923.14 | 28 | 3746.20 | 747.42 | 11.046 | 8.185 | 14.907 | < 0.001 |
| Summer | 28 | 1081.07 | 2590.02 | 35 | 4793.88 | 730.10 | 7.465 | 5.532 | 10.075 | < 0.001 |
| Autumn | 21 | 205.32 | 10,228.13 | 28 | 3561.62 | 786.16 | 27.378 | 20.289 | 36.950 | < 0.001 |
| Winter | 28 | 1023.31 | 2736.22 | 28 | 4065.33 | 688.75 | 8.360 | 6.195 | 11.283 | < 0.001 |
| Urbanization level | ||||||||||
| 1 (The highest) | 42 | 1173.26 | 3579.77 | 42 | 5526.97 | 759.91 | 9.913 | 7.346 | 13.379 | < 0.001 |
| 2 | 35 | 1081.95 | 3234.89 | 42 | 5927.50 | 708.56 | 9.607 | 7.120 | 12.966 | < 0.001 |
| 3 | 0 | 267.33 | 0.00 | 21 | 1360.70 | 1543.33 | 0.000 | – | – | 0.781 |
| 4 (The lowest) | 21 | 322.44 | 6512.77 | 14 | 3351.86 | 417.68 | 32.813 | 24.316 | 44.285 | < 0.001 |
| Level of care | ||||||||||
| Medical center | 21 | 932.95 | 2250.93 | 21 | 5334.73 | 393.65 | 12.033 | 8.917 | 16.240 | < 0.001 |
| Regional hospital | 42 | 1076.64 | 3901.02 | 77 | 6635.84 | 1160.37 | 7.075 | 5.243 | 9.548 | < 0.001 |
| Local hospital | 35 | 835.39 | 4189.64 | 21 | 4196.46 | 500.42 | 17.618 | 13.056 | 23.778 | < 0.001 |
PYs Person-years, Adjusted HR Adjusted Hazard ratio: Adjusted for the variables listed in Table 1, CI Confidence interval
Types of psychiatric disorders in female patients with psychosexual disorders
Table 3 depicts that the cohort with psychosexual disorders, including sexual dysfunctions, paraphilias, and gender identity disorders, were associated with the risk of psychiatric disorders.
Table 3.
Factors of psychiatric disorders stratified by psychosexual disorders subgroup by using Cox regression model
| Psychosexual disorders | Adjusted HR | 95% CI | 95% CI | P |
|---|---|---|---|---|
| Overall (N = 98) | 9.848 | 7.298 | 13.291 | < 0.001 |
| Sexual dysfunctions (N = 42) | 6.488 | 4.808 | 8.757 | < 0.001 |
| Paraphilias (N = 21) | 33.366 | 24.726 | 45.031 | < 0.001 |
| Gender identity disorders (N = 35) | 12.286 | 9.105 | 16.581 | < 0.001 |
PYs Person-years, Adjusted HR Adjusted Hazard ratio: Adjusted for the variables listed in Table 1, CI Confidence interval
Also, there were no significant differences in the times of the psychiatric visits between the two cohorts, even though the cohort with psychosexual disorders had more psychiatric visits than the comparison cohort (3.82 [standard deviation (SD) ± 4.06] vs 3.15 [SD ± 3.97]), without a statistical difference (p = 0.001) (Table S2).
Discussion
Association between psychosexual disorders and the risk of psychiatric disorders
The adjusted HR was 9.848 (95% CI = 7.298—13.291, p < 0.001) in the association between the psychosexual disorders and psychiatric disorders, and the female patients with psychosexual disorders had a 9.8-fold increase in the risk of psychiatric disorders, after the adjustment of age, monthly income, urbanization level, geographic region, and comorbidities. The Kaplan-Meier analysis demonstrated that the cohort with psychosexual disorders had a significantly higher 15-year psychiatric disorders cumulative incidence than the comparison cohort. To the best of our knowledge, this is the first study on the topic of an association between female patients with psychosexual disorders and the risk of psychiatric morbidity. This finding could serve as a reminder for the clinicians to pay much more attention to these patients because of the issues about psychiatric disorders.
Comparison of this study to previous literature
Previous studies have shown the association between psychosexual disorders and psychiatric disorders that included antidepressant-related sexual dysfunctions in patients with depressive or anxiety disorders [16, 45–47], female paraphilia focused and the personality disorders on the forensic psychiatric topics [14, 15], and the FTM gender disorders and depression, post-traumatic stress disorder, anxiety disorders and suicides [12, 13, 48]. However, these studies were mostly conducted in cross-section methods, and our study is unique for the retrospective cohort design, from a larger population-based database. Besides, male patients with psychosexual disorders have been associated with an increased risk of anxiety disorders, depressive disorders, bipolar disorders, sleep disorders, and psychotic disorders, respectively [33]. There were several differences in the risk of different psychiatric disorders in these two studies. The underlying reasons for the difference of risk for psychiatric disorders, between female patients with psychosexual disorders, needs further studies.
Treatment prevalence of psychosexual disorders in this study
Previous studies revealed that the prevalence of female sexual dysfunctions was 30—60%, in different countries [49–52], but we found that there was 0.007% of sexual dysfunctions in this sample of 15-year of follow-up. In the present study, there were 70 paraphilia patients from the database, and the treatment prevalence of female paraphilias was around 0.004% in this LHID. The prevalence of the female paraphilias were 2% in exhibitionistic behaviors in previous studies [25, 53], 4% in voyeuristic behaviors [25, 53], 0.4% in transvestic fetishism [54], and 1% in sadomasochistic activity [55], from surveys in the population of Sweden [25, 53], and Australia [55]. Previous reports have shown that there were 0.003% in Belgium, [56], 0.82% in Japan [57], and 0.023–0.058% in the United States veteran’s populations [12, 58] of FTM gender identity disorder. Furthermore, the present study found that the treatment prevalence of FTM gender identity disorder, was 0.017%, in the duration of the 15 years of follow-up. The discrepancy of the prevalence might be the difference of studies from a claims database or the survey. Cultural differences might also contribute to this difference: previous studies have shown that females have more difficulties in their help-seeking for sex-related problems in Asian countries [59, 60]. However, the present study is the first one for females with psychosexual disorders and the risk of psychiatric disorders in an Asian country.
Possible mechanisms for the increased risk of psychiatric disorders in patients with psychosexual disorders
In the present study, female patients with sexual dysfunctions were associated with psychiatric disorders. There are several neurodevelopmental, endocrine, and psychological factors related to the linkage between these two groups of disorders. The stress from the suffering of sexual dysfunction [61, 62], paraphilias [63, 64], and gender identity disorders [65–67], might well contribute to the association between these psychosexual disorders and the risk of psychiatric disorders, such as anxiety, depressive, or sleep disorders. One study has found that hyperprolactinemia seems to play a role in the pathogenesis of hypoactive sexual desire disorder, one of the female sexual dysfunctions [68], and hyperprolactinemia might induced psychiatric disorders, such as depression and anxiety [69–72].
Evidence suggests that female and male brains are different in the mean volumes of the hippocampus, amygdala, and thalamus [73], the concentration of estrogen or androgen receptors [74], and the total brain, cerebrum, and cerebellum volumes [75]. Thus, the difference in the brain anatomy and neuronal signaling pathways are more closely aligned with a person’s perceived gender identity, and individuals with discordant gonadal and brain developments might experience psychological challenges for the generalized dissatisfaction with their biological sex [76]. Besides, paraphilias and depression might share a common dysregulation of this monoaminergic pathway in these patients [11, 77].
Psychological, social, and cultural factors might also contribute to both psychosexual disorders and psychiatric disorders. Previous studies have shown that patients with paraphilias might suffer emotional distress, social embarrassment [4], and stigma [5]. For example, a study from Turkey has found that patients with vaginismus have higher levels of depression and anxiety [78]. Phobic defense mechanisms [79], the rejection of the female role, and religious orthodoxy which regards sex as dirty or shameful [80] are the psychosocial factors that contribute to vaginismus, depression, and anxiety [78].
Limitations
The present study has several limitations that warrant consideration. First, similar to previous studies using the NHIRD on psychosexual disorders [32, 81–83], we were unable to evaluate the severity, weakness severity, laboratory parameters, or psychological assessments in the patients with psychosexual disorders, since the data were not recorded in the NHIRD. Second, the genetic, psychosocial, and environmental factors, were not included in the dataset. Third, even though we have excluded the patients diagnosed with psychiatric disorders before 2000, or before their first visit for any psychosexual disorders, there is the possibility of the protopathic bias, in which some patients could have been introduced into this study by subjects who have an undiagnosed disease. Fourth, although paraphilias and gender dysphoria are distinct categories, there is some evidence for an overlap between paraphilias and gender dysphoria [84]. The combination of distinct entities, in a single heterogeneous category of psychosexual disorders, is a limitation when discussing the results of the data analysis. Fifth, there is a possibility that the high prevalence of psychiatric disorders, among female patients with psychosexual disorders, is due to the high utilization of psychiatric services. However, as shown in Table S2, there were no significant differences in the times of psychiatric visits between the two cohorts.
Conclusion
Female patients who suffer from psychosexual disorders have a 9.8-fold increase in the risk of psychiatric disorders, and this finding should serve as a timely reminder for the clinicians to pay much more attention to these patients because of their mental health issues.
Supplementary Information
Additional file 1: Table S1. ICD-9-CM codes of Psychosexual disorders.
Additional file 2: Table S2. Frequency of psychiatric service.
Acknowledgements
We appreciate the support from the Tri-Service General Hospital Research Foundation and the Medical Affairs Bureau, Ministry of Defense, Taiwan, ROC. We also appreciate the database provided by the Health and Welfare Data Science Center, Ministry of Health and Welfare (HWDC, MOHW).
Abbreviations
- CCI
Charlson Comorbidity Index
- CI
Confidence interval
- FTM
Female-to-male
- HR
Hazard ratio
- ICD-9-CM
International Classification of Diseases, 9th Revision, Clinical Modification
- LHID
Longitudinal Health Insurance Database
- NHIRD
National Health Insurance Research Database
- NT$
New Taiwan Dollars
Authors’ contributions
IJL: Conceptualization, Investigation, Writing-original draft. NST: Data curation, Funding acquisition, Investigation, Methodology, Resources. CHC: Formal analysis, Investigation, Methodology, Software, Visualization. WCC: Conceptualization, Funding acquisition, Methodology, Project administration, Resources, Supervision, Validation, Writing-review & editing. The author(s) read and approved the final manuscript.
Funding
This study was supported by The Program for Promoting Teaching Excellence Universities, Ministry of Education (NDMC 104–106: I2–4), the Medical Affairs Bureau, Ministry of Defense (MAB-107-084 and MND-MAB-110-087), the Tri-Service General Hospital Foundation (TSGH-C107–004, TSGH-C107–106, TSGH-C108–003, TSGH-C108–151, TSGH-B-109-010, TSGH-E-110240, and TSGH-B-110012), and the Taoyuan Armed Forces General Hospital (TYAFGH-A-110020). The sponsors have no role in study design, data collection, and analysis, decision to publish, or preparation of the manuscript. However, all authors declare no financial interests nor conflict of interest or the appearance of a conflict of interest about the work.
Availability of data and materials
Data are available from the National Health Insurance Research Database (NHIRD) published by the Taiwan National Health Insurance (NHI) Administration. Due to legal restrictions imposed by the government of Taiwan concerning the “Personal Information Protection Act”, data cannot be made publicly available. Requests for data can be sent as a formal proposal to the NHIRD (https://dep.mohw.gov.tw/DOS/lp-2506-113.html).
Ethics approval and consent to participate
This study was conducted according to the Code of Ethics of the World Medical Association (Declaration of Helsinki). The Institutional Review Board of the Tri-Service General Hospital approved this study and waived the need for individual consents since all the identification data were encrypted in the NHIRD (No. 1–106–05-055).
Consent for publication
Not applicable.
Competing interests
None
Footnotes
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Friedman JM, Czekala JE. Psychosexual disorders. In: Morrison RL, Bellack AS, editors. Medical factors and psychological disorders. Boston: Springer; 1987. [Google Scholar]
- 2.Crépault C. Classification of psychosexual disorders. Contracept Fertil Sex. 1993;21(2):177–183. [PubMed] [Google Scholar]
- 3.American Psychiatric Association . Diagnostic and statistical manual of mental disorders. 4. USA: American Psychiatric Association; 1994. [Google Scholar]
- 4.Saleh FM, Berlin FS. Sex hormones, neurotransmitters, and psychopharmacological treatments in men with paraphilic disorders. J Child Sex Abus. 2003;12(3–4):233–253. doi: 10.1300/J070v12n03_09. [DOI] [PubMed] [Google Scholar]
- 5.Jahnke S, Schmidt AF, Geradt M, Hoyer J. Stigma-related stress and its correlates among men with pedophilic sexual interests. Arch Sex Behav. 2015;44(8):2173–2187. doi: 10.1007/s10508-015-0503-7. [DOI] [PubMed] [Google Scholar]
- 6.Hanamsagar R, Bilbo SD. Sex differences in neurodevelopmental and neurodegenerative disorders: focus on microglial function and neuroinflammation during development. J Steroid Biochem Mol Biol. 2016;160:127–133. doi: 10.1016/j.jsbmb.2015.09.039. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Rajkumar RP. Gender identity disorder and schizophrenia: neurodevelopmental disorders with common causal mechanisms? Schizophr Res Treatment. 2014;2014:463757. doi: 10.1155/2014/463757. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Davis SR, Guay AT, Shifren JL, Mazer NA. Endocrine aspects of female sexual dysfunction. J Sex Med. 2004;1(1):82–86. doi: 10.1111/j.1743-6109.2004.10112.x. [DOI] [PubMed] [Google Scholar]
- 9.Foreman M, Hare L, York K, Balakrishnan K, Sanchez FJ, Harte F, Erasmus J, Vilain E, Harley VR. Genetic link between gender dysphoria and sex hormone signaling. J Clin Endocrinol Metab. 2019;104(2):390–396. doi: 10.1210/jc.2018-01105. [DOI] [PubMed] [Google Scholar]
- 10.Walf AA, Frye CA. A review and update of mechanisms of estrogen in the hippocampus and amygdala for anxiety and depression behavior. Neuropsychopharmacology. 2006;31(6):1097–1111. doi: 10.1038/sj.npp.1301067. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Bradford JM. The paraphilias, obsessive compulsive spectrum disorder, and the treatment of sexually deviant behaviour. Psychiatr Q. 1999;70(3):209–219. doi: 10.1023/A:1022099026059. [DOI] [PubMed] [Google Scholar]
- 12.Brown GR, Jones KT. Mental health and medical health disparities in 5135 transgender veterans receiving healthcare in the veterans health administration: a case-control study. LGBT Health. 2016;3(2):122–131. doi: 10.1089/lgbt.2015.0058. [DOI] [PubMed] [Google Scholar]
- 13.Dhejne C, Van Vlerken R, Heylens G, Arcelus J. Mental health and gender dysphoria: a review of the literature. Int Rev Psychiatry (Abingdon, England) 2016;28(1):44–57. doi: 10.3109/09540261.2015.1115753. [DOI] [PubMed] [Google Scholar]
- 14.Segal DL, Gottschling J, Marty M, Meyer WJ, Coolidge FL. Relationships among depressive, passive-aggressive, sadistic and self-defeating personality disorder features with suicidal ideation and reasons for living among older adults. Aging Ment Health. 2015;19(12):1071–1077. doi: 10.1080/13607863.2014.1003280. [DOI] [PubMed] [Google Scholar]
- 15.Turner D, Briken P. Treatment of paraphilic disorders in sexual offenders or men with a risk of sexual offending with luteinizing hormone-releasing hormone agonists: an updated systematic review. J Sex Med. 2018;15(1):77–93. doi: 10.1016/j.jsxm.2017.11.013. [DOI] [PubMed] [Google Scholar]
- 16.Preeti S, Jayaram SD, Chittaranjan A. Sexual dysfunction in patients with antidepressant-treated anxiety or depressive disorders: a pragmatic multivariable longitudinal study. East Asian Arch Psychiatry. 2018;28(1):9–16. [PubMed] [Google Scholar]
- 17.Stein DJ, Phillips KA, Bolton D, Fulford KW, Sadler JZ, Kendler KS. What is a mental/psychiatric disorder? From DSM-IV to DSM-V. Psychol Med. 2010;40(11):1759–1765. doi: 10.1017/S0033291709992261. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Atlantis E, Sullivan T. Bidirectional association between depression and sexual dysfunction: a systematic review and meta-analysis. J Sex Med. 2012;9(6):1497–1507. doi: 10.1111/j.1743-6109.2012.02709.x. [DOI] [PubMed] [Google Scholar]
- 19.Bhasin S, Basson R. Sexual dysfunction in men and women. In: Melmed S, Polonsky KS, Larsen PR, Kronenberg HM, editors. Williams textbook of endocrinology. 13. Philadelphia: Elsevier, Inc; 2016. pp. 785–830. [Google Scholar]
- 20.Yehuda R, Lehrner A, Rosenbaum TY. PTSD and sexual dysfunction in men and women. J Sex Med. 2015;12(5):1107–1119. doi: 10.1111/jsm.12856. [DOI] [PubMed] [Google Scholar]
- 21.Cosgrove DJ, Gordon Z, Bernie JE, Hami S, Montoya D, Stein MB, Monga M. Sexual dysfunction in combat veterans with post-traumatic stress disorder. Urology. 2002;60(5):881–884. doi: 10.1016/S0090-4295(02)01899-X. [DOI] [PubMed] [Google Scholar]
- 22.Hoshiai M, Matsumoto Y, Sato T, Ohnishi M, Okabe N, Kishimoto Y, Terada S, Kuroda S. Psychiatric comorbidity among patients with gender identity disorder. Psychiatry Clin Neurosci. 2010;64(5):514–519. doi: 10.1111/j.1440-1819.2010.02118.x. [DOI] [PubMed] [Google Scholar]
- 23.Simon L, Zsolt U, Fogd D, Czobor P. Dysfunctional core beliefs, perceived parenting behavior and psychopathology in gender identity disorder: a comparison of male-to-female, female-to-male transsexual and nontranssexual control subjects. J Behav Ther Exp Psychiatry. 2011;42(1):38–45. doi: 10.1016/j.jbtep.2010.08.004. [DOI] [PubMed] [Google Scholar]
- 24.Fedoroff JP, Fishell A, Fedoroff B. A case series of women evaluated for Paraphilic sexual disorders. Can J Hum Sex. 1999;8:127. [Google Scholar]
- 25.Dawson SJ, Bannerman BA, Lalumiere ML. Paraphilic interests: an examination of sex differences in a nonclinical sample. Sex Abuse. 2016;28(1):20–45. doi: 10.1177/1079063214525645. [DOI] [PubMed] [Google Scholar]
- 26.Ho Chan WS. Taiwan’s healthcare report 2010. EPMA J. 2010;1(4):563–585. doi: 10.1007/s13167-010-0056-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Chinese Hospital Association . ICD-9-CM English-Chinese Dictionary. Taipei: Chinese Hospital Association Press; 2000. [Google Scholar]
- 28.Ministry of Justice. National Health Insurance Reimbursement Regulations. https://law.moj.gov.tw/LawClass/LawAll.aspx?pcode=L0060035. Accessed 31 Dec 2020.
- 29.Tzeng NS, Chang HA, Chung CH, Lin FH, Yeh CB, Huang SY, Chang CC, Lu RB, Kao YC, Yeh HW, et al. Risk of psychiatric disorders in Guillain-Barre syndrome: a nationwide, population-based, cohort study. J Neurol Sci. 2017;381:88–94. doi: 10.1016/j.jns.2017.08.022. [DOI] [PubMed] [Google Scholar]
- 30.Chien WC, Chung CH, Lin FH, Chang HA, Kao YC, Tzeng NS. Is weight control surgery associated with increased risk of newly onset psychiatric disorders? A population-based, matched cohort study in Taiwan. J Med Sci. 2017;37(4):137–149. doi: 10.4103/jmedsci.jmedsci_94_16. [DOI] [Google Scholar]
- 31.Tzeng NS, Chung CH, Lin FH, Yeh CB, Huang SY, Lu RB, Chang HA, Kao YC, Chiang WS, Chou YC, et al. Headaches and risk of dementia. Am J Med Sci. 2017;353(3):197–206. doi: 10.1016/j.amjms.2016.12.014. [DOI] [PubMed] [Google Scholar]
- 32.Yang YJ, Chien WC, Chung CH, Hong KT, Yu YL, Hueng DY, Chen YH, Ma HI, Chang HA, Kao YC, et al. Risk of erectile dysfunction after traumatic brain injury: a nationwide population-based cohort study in Taiwan. Am J Mens Health. 2018. 10.1177/1557988317750970. [DOI] [PMC free article] [PubMed]
- 33.Tzeng NS, Yeh HW, Chung CH, Chang HA, Kao YC, Chiang WS, Chien WC. Risk of psychiatric morbidity in psychosexual disorders in male patients: a nationwide, cohort study in Taiwan. Am J Mens Health. 2019;13(2):1557988319842985. doi: 10.1177/1557988319842985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Ministry of Justice. Civil Code. https://law.moj.gov.tw/ENG/LawClass/LawAll.aspx?pcode=B0000001. Accessed 31 Dec 2020.
- 35.Kang MS, Choi SH, Koh IS. The effect of increasing control-to-case ratio on statistical power in a simulated case-control SNP association study. Genomics Inform. 2009;7(3):148–151. doi: 10.5808/GI.2009.7.3.148. [DOI] [Google Scholar]
- 36.Grimes DA, Schulz KF. Compared to what? Finding controls for case-control studies. Lancet (London, England) 2005;365(9468):1429–1433. doi: 10.1016/S0140-6736(05)66379-9. [DOI] [PubMed] [Google Scholar]
- 37.McGrogan A, Madle GC, Seaman HE, de Vries CS. The epidemiology of Guillain-Barré syndrome worldwide. Neuroepidemiology. 2009;32(2):150–163. doi: 10.1159/000184748. [DOI] [PubMed] [Google Scholar]
- 38.van den Berg B, Walgaard C, Drenthen J, Fokke C, Jacobs BC, van Doorn PA. Guillain-Barre syndrome: pathogenesis, diagnosis, treatment and prognosis. Nat Rev Neurol. 2014;10(8):469–482. doi: 10.1038/nrneurol.2014.121. [DOI] [PubMed] [Google Scholar]
- 39.Sandoglobulin Guillain-Barre Syndrome Trial Group Randomised trial of plasma exchange, intravenous immunoglobulin, and combined treatments in Guillain-Barre syndrome. Plasma exchange. Lancet (London, England) 1997;349(9047):225–230. doi: 10.1016/S0140-6736(96)09095-2. [DOI] [PubMed] [Google Scholar]
- 40.Austin SR, Wong Y-N, Uzzo RG, Beck JR, Egleston BL. Why summary comorbidity measures such as the Charlson comorbidity index and Elixhauser score work. Med Care. 2015;53(9):e65–e72. doi: 10.1097/MLR.0b013e318297429c. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Deyo RA, Cherkin DC, Ciol MA. Adapting a clinical comorbidity index for use with ICD-9-CM administrative databases. J Clin Epidemiol. 1992;45(6):613–619. doi: 10.1016/0895-4356(92)90133-8. [DOI] [PubMed] [Google Scholar]
- 42.Needham DM, Scales DC, Laupacis A, Pronovost PJ. A systematic review of the Charlson comorbidity index using Canadian administrative databases: a perspective on risk adjustment in critical care research. J Crit Care. 2005;20(1):12–19. doi: 10.1016/j.jcrc.2004.09.007. [DOI] [PubMed] [Google Scholar]
- 43.Marzona I, Baviera M, Vannini T, Tettamanti M, Cortesi L, Riva E, Nobili A, Marcon G, Fortino I, Bortolotti A, et al. Risk of dementia and death in patients with atrial fibrillation: a competing risk analysis of a population-based cohort. Int J Cardiol. 2016;220:440–444. doi: 10.1016/j.ijcard.2016.06.235. [DOI] [PubMed] [Google Scholar]
- 44.Blanche P, Proust-Lima C, Loubere L, Berr C, Dartigues JF, Jacqmin-Gadda H. Quantifying and comparing dynamic predictive accuracy of joint models for longitudinal marker and time-to-event in presence of censoring and competing risks. Biometrics. 2015;71(1):102–113. doi: 10.1111/biom.12232. [DOI] [PubMed] [Google Scholar]
- 45.Clayton AH, Gommoll C, Chen D, Nunez R, Mathews M. Sexual dysfunction during treatment of major depressive disorder with vilazodone, citalopram, or placebo: results from a phase IV clinical trial. Int Clin Psychopharmacol. 2015;30(4):216–223. doi: 10.1097/YIC.0000000000000075. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Jacobsen PL, Mahableshwarkar AR, Palo WA, Chen Y, Dragheim M, Clayton AH. Treatment-emergent sexual dysfunction in randomized trials of vortioxetine for major depressive disorder or generalized anxiety disorder: a pooled analysis. CNS Spectr. 2016;21(5):367–378. doi: 10.1017/S1092852915000553. [DOI] [PubMed] [Google Scholar]
- 47.Olisah VO, Sheikh TL, Abah ER, Mahmud-Ajeigbe AF. Sociodemographic and clinical correlates of sexual dysfunction among psychiatric outpatients receiving common psychotropic medications in a neuropsychiatric hospital in northern Nigeria. Niger J Clin Pract. 2016;19(6):799–806. doi: 10.4103/1119-3077.180063. [DOI] [PubMed] [Google Scholar]
- 48.Ibrahim C, Haddad R, Richa S. Psychiatric comorbidities in transsexualism: study of a Lebanese transgender population. L’Encephale. 2016;42(6):517–522. doi: 10.1016/j.encep.2016.02.011. [DOI] [PubMed] [Google Scholar]
- 49.Nappi RE, Cucinella L, Martella S, Rossi M, Tiranini L, Martini E. Female sexual dysfunction (FSD): prevalence and impact on quality of life (QoL) Maturitas. 2016;94:87–91. doi: 10.1016/j.maturitas.2016.09.013. [DOI] [PubMed] [Google Scholar]
- 50.Zhang C, Tong J, Zhu L, Zhang L, Xu T, Lang J, Xie Y. A population-based epidemiologic study of female sexual dysfunction risk in mainland China: prevalence and predictors. J Sex Med. 2017;14(11):1348–1356. doi: 10.1016/j.jsxm.2017.08.012. [DOI] [PubMed] [Google Scholar]
- 51.Lou WJ, Chen B, Zhu L, Han SM, Xu T, Lang JH, Zhang L. Prevalence and factors associated with female sexual dysfunction in Beijing, China. Chin Med J. 2017;130(12):1389–1394. doi: 10.4103/0366-6999.207466. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Singh JC, Tharyan P, Kekre NS, Singh G, Gopalakrishnan G. Prevalence and risk factors for female sexual dysfunction in women attending a medical clinic in South India. J Postgrad Med. 2009;55(2):113–120. doi: 10.4103/0022-3859.52842. [DOI] [PubMed] [Google Scholar]
- 53.Langstrom N, Seto MC. Exhibitionistic and voyeuristic behavior in a Swedish national population survey. Arch Sex Behav. 2006;35(4):427–435. doi: 10.1007/s10508-006-9042-6. [DOI] [PubMed] [Google Scholar]
- 54.Langstrom N, Zucker KJ. Transvestic fetishism in the general population: prevalence and correlates. J Sex Marital Ther. 2005;31(2):87–95. doi: 10.1080/00926230590477934. [DOI] [PubMed] [Google Scholar]
- 55.Richters J, de Visser RO, Rissel CE, Grulich AE, Smith AM. Demographic and psychosocial features of participants in bondage and discipline, “sadomasochism” or dominance and submission (BDSM): data from a national survey. J Sex Med. 2008;5(7):1660–1668. doi: 10.1111/j.1743-6109.2008.00795.x. [DOI] [PubMed] [Google Scholar]
- 56.De Cuypere G, Van Hemelrijck M, Michel A, Carael B, Heylens G, Rubens R, Hoebeke P, Monstrey S. Prevalence and demography of transsexualism in Belgium. Eur Psychiatry. 2007;22(3):137–141. doi: 10.1016/j.eurpsy.2006.10.002. [DOI] [PubMed] [Google Scholar]
- 57.Baba T, Endo T, Ikeda K, Shimizu A, Honnma H, Ikeda H, Masumori N, Ohmura T, Kiya T, Fujimoto T, et al. Distinctive features of female-to-male transsexualism and prevalence of gender identity disorder in Japan. J Sex Med. 2011;8(6):1686–1693. doi: 10.1111/j.1743-6109.2011.02252.x. [DOI] [PubMed] [Google Scholar]
- 58.Blosnich JR, Brown GR, Shipherd Phd JC, Kauth M, Piegari RI, Bossarte RM. Prevalence of gender identity disorder and suicide risk among transgender veterans utilizing veterans health administration care. Am J Public Health. 2013;103(10):e27–e32. doi: 10.2105/AJPH.2013.301507. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 59.Vahdaninia M, Montazeri A, Goshtasebi A. Help-seeking behaviors for female sexual dysfunction: a cross sectional study from Iran. BMC Womens Health. 2009;9:3. doi: 10.1186/1472-6874-9-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 60.Moreira ED, Jr, Kim SC, Glasser D, Gingell C. Sexual activity, prevalence of sexual problems, and associated help-seeking patterns in men and women aged 40-80 years in Korea: data from the Global Study of Sexual Attitudes and Behaviors (GSSAB) J Sex Med. 2006;3(2):201–211. doi: 10.1111/j.1743-6109.2006.00210.x. [DOI] [PubMed] [Google Scholar]
- 61.Hamilton LD, Meston CM. Chronic stress and sexual function in women. J Sex Med. 2013;10(10):2443–2454. doi: 10.1111/jsm.12249. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 62.Yazdanpanahi Z, Nikkholgh M, Akbarzadeh M, Pourahmad S. Stress, anxiety, depression, and sexual dysfunction among postmenopausal women in Shiraz, Iran, 2015. J Fam Community Med. 2018;25(2):82–87. doi: 10.4103/jfcm.JFCM_117_17. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 63.Bradford JM, Ahmed AG. The natural history of the paraphilias. Psychiatr Clin North Am. 2014;37(2):xi–xv. doi: 10.1016/j.psc.2014.03.010. [DOI] [PubMed] [Google Scholar]
- 64.Kuzma JM, Black DW. Epidemiology, prevalence, and natural history of compulsive sexual behavior. Psychiatr Clin North Am. 2008;31(4):603–611. doi: 10.1016/j.psc.2008.06.005. [DOI] [PubMed] [Google Scholar]
- 65.Colizzi M, Costa R, Pace V, Todarello O. Hormonal treatment reduces psychobiological distress in gender identity disorder, independently of the attachment style. J Sex Med. 2013;10(12):3049–3058. doi: 10.1111/jsm.12155. [DOI] [PubMed] [Google Scholar]
- 66.Matsumoto Y, Sato T, Ohnishi M, Kishimoto Y, Terada S, Kuroda S. Stress-coping strategies of patients with gender identity disorder. Psychiatry Clin Neurosci. 2009;63(6):715–720. doi: 10.1111/j.1440-1819.2009.02017.x. [DOI] [PubMed] [Google Scholar]
- 67.Wallien MS, van Goozen SH, Cohen-Kettenis PT. Physiological correlates of anxiety in children with gender identity disorder. Eur Child Adolesc Psychiatry. 2007;16(5):309–315. doi: 10.1007/s00787-007-0602-7. [DOI] [PubMed] [Google Scholar]
- 68.Corona G, Petrone L, Mannucci E, Ricca V, Balercia G, Giommi R, Forti G, Maggi M. The impotent couple: low desire. Int J Androl. 2005;28(Suppl 2):46–52. doi: 10.1111/j.1365-2605.2005.00594.x. [DOI] [PubMed] [Google Scholar]
- 69.Hinojosa-Amaya JM, Johnson N, González-Torres C, Varlamov EV, Yedinak CG, McCartney S, Fleseriu M. Depression and impulsivity self-assessment tools to identify dopamine agonist side effects in patients with pituitary adenomas. Front Endocrinol (Lausanne) 2020;11:579606. doi: 10.3389/fendo.2020.579606. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 70.Ioachimescu AG, Fleseriu M, Hoffman AR, Vaughan Iii TB, Katznelson L. Psychological effects of dopamine agonist treatment in patients with hyperprolactinemia and prolactin-secreting adenomas. Eur J Endocrinol. 2019;180(1):31–40. doi: 10.1530/EJE-18-0682. [DOI] [PubMed] [Google Scholar]
- 71.Krysiak R, Szkróbka W, Okopień B. The effect of bromocriptine treatment on sexual functioning and depressive symptoms in women with mild hyperprolactinemia. Pharmacol Rep. 2018;70(2):227–232. doi: 10.1016/j.pharep.2017.10.008. [DOI] [PubMed] [Google Scholar]
- 72.Liao WT, Bai YM. Major depressive disorder induced by prolactinoma--a case report. Gen Hosp Psychiatry. 2014;36(1):125.e121–125.e122. doi: 10.1016/j.genhosppsych.2013.01.010. [DOI] [PubMed] [Google Scholar]
- 73.Ritchie SJ, Cox SR, Shen X, Lombardo MV, Reus LM, Alloza C, Harris MA, Alderson HL, Hunter S, Neilson E, et al. Sex differences in the adult human brain: evidence from 5216 UK biobank participants. Cereb Cortex. 2018;28(8):2959–2975. doi: 10.1093/cercor/bhy109. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 74.Halpern D. Sex differences in cognitive abilities. New York: Psychology Press; 2012. [Google Scholar]
- 75.Ruigrok AN, Salimi-Khorshidi G, Lai MC, Baron-Cohen S, Lombardo MV, Tait RJ, Suckling J. A meta-analysis of sex differences in human brain structure. Neurosci Biobehav Rev. 2014;39(100):34–50. doi: 10.1016/j.neubiorev.2013.12.004. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 76.Boucher FJO, Chinnah TI. Gender dysphoria: a review investigating the relationship between genetic influences and brain development. Adolesc Health Med Ther. 2020;11:89–99. doi: 10.2147/AHMT.S259168. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 77.Garcia FD, Thibaut F. Current concepts in the pharmacotherapy of paraphilias. Drugs. 2011;71(6):771–790. doi: 10.2165/11585490-000000000-00000. [DOI] [PubMed] [Google Scholar]
- 78.Karaguzel E, Arslan F, Tiryaki A, Osmanagaoglu M, Kaygusuz E. Sociodemographic features, depression and anxiety in women with life-long vaginismus. Anatolian J Psychiatry. 2016;17(6):1. doi: 10.5455/apd.215372. [DOI] [Google Scholar]
- 79.Fugl-Meyer KS, Bohm-Starke N, Damsted Petersen C, Fugl-Meyer A, Parish S, Giraldi A. Standard operating procedures for female genital sexual pain. J Sex Med. 2013;10(1):83–93. doi: 10.1111/j.1743-6109.2012.02867.x. [DOI] [PubMed] [Google Scholar]
- 80.Rao TS, Nagaraj AK. Female sexuality. Indian J Psychiatry. 2015;57(Suppl 2):S296–S302. doi: 10.4103/0019-5545.161496. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 81.Chen KF, Liang SJ, Lin CL, Liao WC, Kao CH. Sleep disorders increase risk of subsequent erectile dysfunction in individuals without sleep apnea: a nationwide population-base cohort study. Sleep Med. 2016;17:64–68. doi: 10.1016/j.sleep.2015.05.018. [DOI] [PubMed] [Google Scholar]
- 82.Hou PH, Mao FC, Chang GR, Huang MW, Wang YT, Huang SS. Newly diagnosed bipolar disorder and the subsequent risk of erectile dysfunction: a nationwide cohort study. J Sex Med. 2018;15(2):183–191. doi: 10.1016/j.jsxm.2017.12.013. [DOI] [PubMed] [Google Scholar]
- 83.Liu HL, Lee HM, Chung YC. Dyspareunia and its comorbidities among Taiwanese women: analysis of the 2004-2010 nationwide health insurance database. J Sex Med. 2015;12(4):1012–1018. doi: 10.1111/jsm.12820. [DOI] [PubMed] [Google Scholar]
- 84.Zucker K, Seto M. Rutter’s child and adolescent psychiatry. 6. 2015. Gender dysphoria and paraphilic sexual disorders; pp. 983–998. [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Additional file 1: Table S1. ICD-9-CM codes of Psychosexual disorders.
Additional file 2: Table S2. Frequency of psychiatric service.
Data Availability Statement
Data are available from the National Health Insurance Research Database (NHIRD) published by the Taiwan National Health Insurance (NHI) Administration. Due to legal restrictions imposed by the government of Taiwan concerning the “Personal Information Protection Act”, data cannot be made publicly available. Requests for data can be sent as a formal proposal to the NHIRD (https://dep.mohw.gov.tw/DOS/lp-2506-113.html).

