Risk factors for an anxiety disorder comorbidity among Thai patients with bipolar disorder: results from the Thai Bipolar Disorder Registry
Authors Paholpak S, Kongsakon R, Pattanakumjorn W, Kanokvut R, Wongsuriyadech W, Srisurapanont M
Received 3 November 2013
Accepted for publication 3 February 2014
Published 15 May 2014 Volume 2014:10 Pages 803—810
Checked for plagiarism Yes
Review by Single-blind
Peer reviewer comments 2
Suchat Paholpak,1 Ronnachai Kongsakon,2 Wasana Pattanakumjorn,3 Roongsang Kanokvut,4 Wiroj Wongsuriyadech,5 Manit Srisurapanont6
On behalf of the Thai Bipolar Disorder Registry Study Group
1Department of Psychiatry, Faculty of Medicine, Khon Kaen University, Khon Kaen, 2Department of Psychiatry, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, 3Department of Psychiatry, Ratchaburi Hospital, Ratchaburi, 4Department of Psychiatry, Buddhachinaraj Hospital, Phitsanulok, 5Department of Psychiatry, Udonthani Hospital, Udonthani, 6Department of Psychiatry, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand
Background: The aim of the study was to determine in a clinical setting the risk factors for current anxiety disorder (AD) comorbidity among Thai patients with bipolar disorder (BD), being treated under the Thai Bipolar Disorder Registry Project (TBDR).
Methods: The TBDR was a multisite naturalistic study conducted at 24 psychiatric units (ie, at university, provincial mental, and government general hospitals) between February 2009 and January 2011. Participants were in- or out-patients over 18 years of age who were diagnosed with BD according to the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition. Instruments used in this study included the Thai Mini International Neuropsychiatric Interview version 5; Thai Montgomery–Åsberg Depression Rating Scale (MADRS); Thai Young Mania Rating Scale; Clinical Global Impression of Bipolar Disorder-Severity (CGI-BP-S), CGI-BP-S-mania, CGI-BP-S-depression, and CGI-BP-S-overall BP illness; and the Thai SF-36 quality of life questionnaire.
Results: Among the 424 BD patients, 404 (95.3%) had BD type I. The respective mean ± standard deviation of age of onset of mood disturbance, first diagnosis of BD, and first treatment of BD was 32.0±11.9, 36.1±12.2, and 36.2±12.2 years. The duration of illness was 10.7±9.0 years. Fifty-three (12.5%) of the 424 participants had a current AD while 38 (9%) had a substance use disorder (SUD). The univariate analysis revealed 13 significant risks for current AD comorbidity, which the multivariate analysis narrowed to age at first diagnosis of BD (odds ratio =0.95, P<0.01), family history of SUD (odds ratio =2.18, P=0.02), and having a higher current MADRS score (odds ratio =1.11, P<0.01).
Conclusion: A diagnosis of AD comorbid with BD is suggested by early-age onset of BD together with a higher MADRS score and a family history of SUD. The likelihood of AD comorbidity decreases by 5% with each passing year; early-age onset of BD is a risk while later age onset is protective. Our results underscore how SUD within the family significantly contributes to the risk of an AD comorbidity.
Keywords: bipolar disorders, risk, protect, anxiety, comorbid, Thai
Bipolar disorder (BD) is a highly prevalent mental illness affecting 2.4% of the worldwide population.1 In Thailand, the prevalence of BD as assessed in 2003 using the Thai Mini International Neuropsychiatric Interview (MINI) was 0.65%.2 The disorder is characterized by mood episodes comprising mania alternating with depression. The clinical course of BD is chronic and typically spans an entire segment in the life of a patient.3 The chronicity of BD results in a high rate of recurrence and a number of psychiatric or medical comorbidities, including anxiety disorder (AD), substance use disorder (SUD), attention-deficit/hyperactivity disorders, personality disorders, migraine, hypothyroidism, and/or diabetes.4
AD is a common – and perhaps the most common – comorbidity5 in patients with BD during either manic, depressive episodes or even during euthymic state.6,7 A large cohort study described a higher incidence of comorbid AD in BD patients than in the general population.8,9 In a prospective follow-up, BD patients with a comorbid social phobia have a longer mood duration and greater severity of illness than those without.10 Comorbid obsessive compulsive disorder (OCD) has a history of a shorter period of euthymia.11 Compared with BD alone, patients with comorbid AD have a higher burden of BD symptoms, greater severity, and sometimes manifestation of a different clinical pattern than BD alone.8 A greater number of attempted suicides are also associated with OCD, panic disorder (PD), and social phobia comorbidity.9 BD patients with comorbid AD need more complex clinical management and treatment because of the prolonged severity of disease burden, which in turn causes more problems with sleep and impairs work and social functioning.8 This population does not, however, usually receive appropriate treatment.9,11
The risk factors for having comorbid suicidality12 and SUD13 in BD have been widely studied. Antypa et al reported that the strongest risk factor for a future suicide event is a prior history of suicide attempts, the other potential risk factors includes younger age, personality disorder traits, and a high percentage of days spent depressed.14 Risk factors for SUD in BD are lifetime oppositional defiant disorder, any lifetime AD, adolescent-onset BD, and suicide attempt(s).15
To date, only a few reports have been conducted on the risk factors for comorbid AD in BD. Using the Diagnostic Interview for Genetic Studies in patients with either bipolar or schizoaffective disorder, Saunders et al found that a) being younger at onset of BD is a risk factor for OCD comorbidity for both sexes, and b) experiencing more antidepressant trials is a risk factor for OCD, PD, and specific phobia in both sexes.8 A community mental health survey in Canada revealed a comorbid mood and AD was more likely for those a) being young, unmarried, and not fully employed, b) having a medical condition, c) experiencing greater than normal levels of stress, d) rating oneself poorer for mental health, and e) being dissatisfied with life.16 The aforementioned studies,8,16 however, were done in particular groups of patients or individuals and mostly in Western countries. We wanted to investigate the similarities and differences in clinical risk factors for current AD in comorbidity with BD in a large sample of patients with BD in a naturalistic clinical Asian setting.
The Thai Bipolar Disorder Registry Project (TBDR) was established nationwide to observe the clinical course of Thai patients with BD over a 1-year period.17 The Registry also collected data regarding clinical parameters, including current comorbidities at baseline. The baseline data were analyzed for risk factors associated with the current ADs comorbidity in Thai patients with BD. The objective of the study was to examine the demographics and clinical characteristics of, and risk factors associated with, current ADs in comorbidity with BD in Thai patients.
Materials and methods
The TBDR was a 1-year multisite, prospective, naturalistic clinical study, conducted between February 2009 and January 2011 in Thailand. The TBDR comprised 24 psychiatric servicing units at various hospitals (ie, university, provincial general, and mental). The primary objective was to characterize the course of BD illness among a sample of Thai patients. The study did not involve any clinical management of the participants. The reader can find details in a recent article.17 The institutional review board at each site approved the protocol.
Participants in this study were the bipolar I and II patients attending psychiatric services during the study period, either as out-patients or in-patients at any of the investigation sites. Patients with BD in the study had to meet the following inclusion criteria: a) in- or out-patient diagnosed with BD according to the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV), b) over 18 years of age, c) receiving treatment for BD at one of the research sites during the study period, d) literate in Thai, e) able to make return visits to the hospital every 2 months, and f) able to provide informed written consent after having the details of the study fully explained.
BD patients with any of the following criteria were excluded: a) participating in other research, b) having difficulty traveling, and c) not able to give informed consent.
Patients who fulfilled the study criteria were invited to participate in the study. All participants were assessed at baseline (visit 1) and every 2 (±1) months for 12 months (visit 7). Data collected at baseline included a) demographic details, b) history of BD illness, c) current status of BD (ie, any one of the following: recovered, recovering, roughening, continued symptomatic, major depressive episode, manic episode, hypomanic episode, and/or mixed episode), d) concurrent comorbid psychiatric (any AD and SUD) and nonpsychiatric medical disorder(s)/disease(s), e) current suicidal risk, f) current psychiatric treatment, g) health status (including vital signs, physical examinations, and clinical laboratory tests), and h) quality of life.
The Thai MINI was used to establish the DSM-IV diagnosis of BD I and BD II, current BD illness status, concurrent comorbid psychiatric disorder, and current suicidal risk. The Thai MINI is a structured diagnostic psychiatric interview for the DSM-IV and the International Classification of Diseases-10, which has been translated into Thai. The validity of the Thai MINI has been tested against interviews conducted by Thai Medical Council Board-certified psychiatrists. The MINI has several modules, but the ones chosen for this study are specifically used for diagnosing major depressive episode, (hypo)manic, ADs (generalized AD, OCD, phobic disorder and/or PD), SUD (alcohol and nonalcohol use disorder), and suicide risk.
The respective time-frames required when using the MINI to make a psychiatric diagnosis of a) major depressive episode, b) (hypo)manic episode, c) PD, agoraphobia, social phobia, OCD, d) generalized AD, e) alcohol and nonalcohol psychoactive SUD and f) current suicidal risk are 2 weeks, 1 week, 1 month, 6 months, 12 months, and 1 month.
Udomratn and Kittirattanapaiboon, in 2004, evaluated the interrater reliability, sensitivity, and specificity of the Thai MINI for various entities. The respective interrater reliability (Cohen’s k), sensitivity, and specificity of the module for major depressive episode was 0.84, 0.98, and 0.94; (hypo)manic episode 0.78, 0.89, and 0.94; PD 1.0, 1.0, and 1.0; PD with agoraphobia 0.48, 0.60, and 0.98; PD without agoraphobia 0.74, 0.60, and 1.0; agoraphobia 0.31, 0.50, and 0.94; social phobia 0.35, 0.43, and 0.96; OCD 0.32, 0.44, and 0.95; generalized AD 0.89, 1.00, and 0.97; alcohol dependence 0.74, 0.92, and 0.93; alcohol abuse 0.40, 0.41, and 0.95; substance dependence 0.92, 0.95, and 0.99; substance abuse incomputable, incomputable, and 0.99; and suicidal risk 0.86, 0.96, and 0.91.18
The severity of symptoms and syndrome of (hypo)manic episode were measured using the Thai Young Mania Rating Scale (interrater reliability [Pearson’s correlation] 0.87, Cronbach’s a coefficient 0.89).19 Major depressive episodes were measured using the Thai Montgomery–Åsberg Depression Rating Scale (MADRS) (interrater reliability [Cohen’s k] 0.78, Cronbach’s a coefficient 0.80).20 The overall severity of the current mood status was evaluated using the Clinical Global Impression of Bipolar Disorder-Severity (CGI-BP-S): CGI-BP-S-mania, CGI-BP-S-depression and CGI-BP-S-overall BP illness.21 All of these measures were administered by MINI-trained psychiatrists with experience in clinical studies involving BD patients. Quality of life was measured using the Thai version of the self-rating SF-36 questionnaire (test–retest reliability [Pearson’s correlation] 0.6, Cronbach’s α coefficient 0.92).22 The SF-36 is a self-rating questionnaire comprising eight domains with 100 marks for each domain, including mental health, general health, bodily pain, physical functioning, role physical, role emotional, vitality, and social functioning.
In order to comply with the objectives of the current study, only data at baseline were used for analysis. The institutional review board at each site approved the protocol. Patients were asked to give informed, written consent before participating in the study.
The main objective of the study was analyzed with descriptive statistics exclusively. Total values and percentages were used for the categorical variables while means with standard deviations (SD) were used for the quantitative variables. A comparative analysis was done using bivariate and multivariate analyses. The Student’s t-test and the χ2-test were used for the bivariate analyses while logistical regression was used for the multivariate analyses. A value P≤0.05 was considered statistically significant.
The present study recruited 424 patients with BD, of whom 404 (95.3%) had BD type I.
The patients averaged 42.7±12.3 years of age. Most (258; 60.8%) were female, 211 (49.9%) were married, 147 (34.8%) were single, and the remaining 57 patients (15.3%) were divorced or widowed. The majority (276; 65.3%) had less than 12 years of education.
One hundred and thirty-two (31.2%) of the 423 participants had some type of psychiatric disorder and four of the patients (3.0%) had SUD in the family.
Prevalence of comorbidity
Fifty-three (12.5%) of the 424 BD participants had some kind of current AD: 18 (34.0%) generalized AD, 15 (28.3%) OCD, 13 (24.5%) agoraphobia, nine (17.0%) social phobia, and seven (13.2%) PD. Thirty-eight (9%) patients had SUD of some kind (alcohol or nonalcohol).
Course of illness
The respective age at onset of mood disturbance, first diagnosis of BD, first treatment of BD, and duration of BD illness was 32.0±11.9, 36.1±12.2, 36.2±12.2, and 10.7±9.0 years.
At baseline, 255 (60.1%) patients were in recovery, 48 (11.3%) were recovering, three (0.7%) were roughening, 26 (6.1%) continued symptomatic, 30 (7.1%) depressed, 29 (6.8%) manic, 20 (4.7%) mixed, and 13 (3.2%) hypomanic. Eleven (2.6%) and nine (2.1%) of the patients had moderate and high suicidal risk, respectively.
Quality of life
Scores for the SF-36 Thai version of the whole sample at baseline were a) physical functioning 81.8±20.0, b) role physical 70.2±40.2, c) bodily pain 76.4±23.3, d) general health 58.1±22.8, e) vitality 60.4±16.3, f) social functioning 77.3±24.1, g) role emotional 63.9±42.1, and h) mental health 70.0±18.3.
Clinical parameters (variables) were analyzed one by one for any association they might have with AD comorbidity. None of the demographic data had any statistically significant association with comorbid AD, including subtype of BD (BD I or BD II, P=0.47), sex (P=0.10), marital status (P=0.32), and educational level (P=0.57). Family history of psychiatric illness and SUD also did not have any statistically significant association with the comorbid AD (P=0.26 and P=0.37, respectively). Some variables regarding the course of illness did, however, have positive associations, including earlier age onset of mood disturbance (P=0.02), earlier age of BD onset (P=0.04), earlier age at the first treatment for BD (P=0.05), mixed polarity at the first mood episode (P≤0.01), and history of rapid cycling (P=0.05).
Variables at baseline identified as having a positive association with comorbid AD included current younger age (P=0.008), depressive polarity of the current mood episode (P<0.01), high suicidality (P<0.01), and higher score in the clinical psychometric scale (ie, Thai Young Mania Rating Scale, Thai MADRS, CGI-BP-S-mania, CGI-BP-S-depression, and CGI-BP-S-overall BP illness; P≤0.05). BD patients with comorbid AD, compared with those without the comorbidity, had a lower quality of life as assessed by the SF-36 in almost all domains (P<0.01 for every domain, with the exception of P=0.03 for the domain of physical functioning). The presence of comorbid SUD was not significantly associated with AD comorbidity (P=0.45) (Table 1).
Interactions among variables and AD comorbidity were inferred from the regression model of the multivariate analysis. Variables entered into the model included all those with a P≤0.2 from the univariate analyses. SUD, whether present in the family or in the patient, even if the P>0.2, was also entered into the model of analysis because of its theoretical association with BD.23 In the final step of the regression analysis, the variables that still had a statistical significant positive association with AD comorbidity were age at onset of BD (odds ratio =0.95, 95% confidence interval [CI] =0.93–0.97, P<0.01), SUD in the patient’s family (odds ratio =2.18, 95% CI =1.11–4.27, P=0.02), and a higher MADRS (odds ratio =1.10, 95% CI =1.06–1.15, P<0.01) (Table 2).
This is the first study on the risk factors for comorbid AD among patients with BD in Thailand. We utilized univariate and multivariate analyses to identify clinical parameters that would be a risk factor for AD comorbidity. One parameter identified was the age at onset of BD. Due to an odds ratio of 0.95, with a 95% CI of 0.93–0.97, this risk could be interpreted in two ways: 1) early onset could be a risk factor and 2) later onset could be a protective factor. Since the odds ratio was 0.95, it means that for every 1-year increment of the onset of BD, there would be a 5% reduction in the chance of having AD comorbidity.
Our finding that early-age onset of BD is a risk factor for AD comorbidity agrees with the finding of others including Etain et al24 and Azorin et al.25 Besides its association with AD comorbidity, early-age onset of BD is also found to be in association with comorbid SUD.25 Our results, therefore, make an important contribution to the knowledge of onset risk, as we observed that later onset of BD was associated with a reduced risk of AD comorbidity.
In another facet, children and adolescents exposed to SUD at home encountered problems with respect to attachment, nurturing, socialization, economic hardship, breaking the law, emotional distress, and violence.26 These children also have an increased risk for internalizing problems such as anxiety, depression, and substance abuse.26,27 The whole family and each family member in this situation are affected by the individual(s) using substances.27 Accordingly, SUD in the family was another factor that our study identified as having a significant association with comorbid AD (odds ratio 2.18). Since there was, however, a very low number of patients having such a family history (four patients), generalization of this result should be done with caution.
Regarding the importance of depressive episode in BD, previous studies indicate that a greater number of depressive episodes is a risk factor for comorbid anxiety and mood disorders28 and that greater severity of depression is a risk factor for suicidality in BD.29 In addition, our study identified that a higher rating in depression scale (MADRS score) was another risk factor for AD comorbidity.
BD patients with comorbid AD frequently face multiple dimensions of physical and psychosocial problems, including sleep disorder, working impairments, and social functioning.8 Relatedly, we found that patients with comorbid AD possessed significant impairments in quality of life (SF-36 score) in almost all functional domains.
Importantly, the prevalence of current comorbid AD among our BD patients (12.5%) was lower than in other studies; Das,6 Simon et al,9 and Gao et al30 reported 29.6%, 30.5%, and 74%, respectively. Possible explanations for the lower prevalence include differences in the methods of diagnosis for comorbid AD (ie, the Thai MINI used in the present study versus the Hamilton Rating Scale for Anxiety used by Das) or the state of illness (ie, the majority of patients in the present study were already in the recovered state [60.1%]), so the therapeutic process leading to this inactive states might altogether obviate the current AD comorbidity. In support of this notion, our results showed that patients in an active state (eg, depressive or mixed or manic) possessed a higher rate of comorbid AD than those in a recovered state (16.0% to 76.5% versus 8.5%) (Table 1). In addition, BD I was diagnosed in the majority (95.3%) of the patients in the present study, which contrasts with Western reports, where prevalence of BD II is more frequent.31 BD I is reported to have a lower rate of AD comorbidity than BD II,32 and indeed the prevalence of AD comorbidity in BD can vary widely.33
As comorbid ADs have a critical impact on the course of BD, for example, worse outcome regarding global and specific measures (namely, illness severity, proportion of the year spent psychologically ill or healthy), the risk factors identified in our report could alert clinicians to the presence of comorbid AD so that appropriate prevention and treatment can be promptly implemented.
The risk factors for comorbidity of AD in patients with BD were early-age onset of the disorder, SUD in the family, and greater intensity of the current depression. Later onset of BD seems to be protective as onset of this comorbidity falls by 5% with each passing year. The present study also underscores the seriousness of SUD within the family as an associated risk.
The present study had some limitations: a) there was no control group; b) some demographic and course of illness data were subject to recall bias; c) the study was a substudy of the TBDR registry, which was designed to ascertain the mood patterns over a 1-year observational period, thus a more specific tool for anxiety assessment (ie, Hamilton Rating Scale for Anxiety) was not employed; d) many sites in the current study were in a psychiatric unit of a general hospital; and e) the risk factors for substance abuse can differ across cultures, and our sample was limited to the Thai population.
This study was supported by an unrestricted research grant from Sanofi-Aventis (Thailand) Ltd. The company did not have any influence on the study design, analysis plan, or preparation of the manuscript. Dr Panadda Klamsum of Sanofi-Aventis (Thailand) Ltd provided administrative support. Assistance with the statistical analysis was provided by statisticians from Sanofi-Aventis (Thailand) Ltd, namely, Ms Taweeporn Natesamroeng, Dr Suthat Chottanapund, and Dr Jaruek Charoensap.
We thank the Thai Bipolar Registry Study Group for its contributions in data collection. The group included Buddhachinnaraj Hospital: R Kanokvut, P Lengdee, and U Wilekha; Chachoengsao Hospital: W Pratoomsri; Galya Rajanagarindra Institute: W Thomkapanich; Institute of Aviation Medicine: P Onsiri; Khon Kaen Rajanagarindra Psychiatric Hospital: K Kittiwattanagul; King Chulalongkorn Memorial Hospital: P Lueboonthavatchai, C Roomruangwong, and S Tangwongchai; Maharaj Nakorn Chiang Mai Hospital: M Srisurapanont, and S Sutthijit; Phrae Hospital: S Tongprasert; Phramongkutklao Hospital: T Leelahanaj; Phrapokklao Hospital: S Sarakul; Prasrimahabhodhi Psychiatric Hospital: S Janthong and T Kongsuk; Rajavithi Hospital: P Thomyangkoon; Ramathibodi Hospital: P Ittasakul and R Kongsakon; Ratchaburi Hospital: S Limsiroratana and W Pattanakumjorn; Rayong Hospital: P Pattaranuthaporn; Siriraj Hospital: S Bussaratid; Somdet Chaopraya Institute of Psychiatry: W Chanakul and P Losatiankij; Srinagarind Hospital: S Paholpak; Srithanya Hospital: S Choovanichvong; Suansaranrom Psychiatric Hospital: S Joowong; Surin Hospital: K Surapongpiwattana and T Surapongpiwattana; Thammasat University Hospital: L Kosulwit; Udonthani Hospital: W Wongsuriyadech; Vachira Phuket Hospital: T Sumpatanarax. We also thank Mr Bryan Roderick Hamman for assistance with the English language presentation of the manuscript.
The following authors have received consulting fees, research grants, and/or honoraria from industry but none related to this work: Dr Suchat Paholpak from AstraZeneca, Janssen, Novartis, Pfizer, Sanofi-Aventis, and Thai Otsuka; Dr Ronnachai Kongsakon from AstraZeneca, Janssen, Novartis, Pfizer, Sanofi-Aventis, and Thai Otsuka; Dr Manit Srisurapanont from AstraZeneca, GlaxoSmithKline, Pfizer, Janssen, Johnson and Johnson, Lundbeck, Sanofi-Aventis, Servier, and Thai Otsuka. The other authors report no conflicts of interest in this work.
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