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. 2018 Jun 3;2018:8463632. doi: 10.1155/2018/8463632

Burden of Depression among Working-Age Adults with Rheumatoid Arthritis

Arijita Deb 1,, Nilanjana Dwibedi 1, Traci LeMasters 1, Jo Ann Hornsby 2, Wenhui Wei 3, Usha Sambamoorthi 1
PMCID: PMC6008693  PMID: 29971163

Abstract

Objective

This study estimated the excess clinical, humanistic, and economic burden associated with depression among working-age adults with Rheumatoid Arthritis (RA).

Methods

A retrospective cross-sectional study was conducted among working-age (18 to 64 years) RA patients with depression (N = 647) and without depression (N = 2,015) using data from the nationally representative Medical Expenditure Panel Survey for the years 2009, 2011, 2013, and 2015.

Results

Overall, 25.8% had depression. In adjusted analyses, adults with RA and depression compared to those without depression were significantly more likely to have pain interference with normal work (severe pain: AOR = 2.22; 95% CI = 1.55, 3.18), functional limitations (AOR = 2.17; 95% CI = 1.61, 2.94), and lower mental health HRQoL scores. Adults with RA and depression had significantly higher annual healthcare expenditures ($14,752 versus 10,541, p < .001) and out-of-pocket spending burden. Adults with RA and depression were more likely to be unemployed and among employed adults, those with depression had a significantly higher number of missed work days annually and higher lost annual wages due to missed work days.

Conclusions

This study highlights the importance of effectively managing depression in routine clinical practice of RA patients to reduce pain and functional limitations, improve quality of life, and lower direct and indirect healthcare costs.

1. Introduction

Rheumatoid Arthritis (RA) is one of the most debilitating chronic conditions, with the onset often occurring during the prime working years of lives, between the ages of 20 and 40 years [1]. Individuals with RA experience substantial pain and RA causes permanent work disability in more than one-third of affected patients within 10 years of onset [2]. Such pain and disabilities associated with RA may contribute to a higher prevalence of depression in individuals with RA compared to healthy controls [3]. An expert review of depression in arthritis reported that the prevalence of depression in adults with RA can be as high as 66.2% [4]. A systematic review and meta-analysis of 72 studies estimated the prevalence rate to be 16.8% [5].

The disease burden of depression in RA can be substantial because depression can worsen survival [6] and increase morbidity in terms of disability, health-related quality of life (HRQoL), RA disease activity [7], and pain [8]. Depression in RA can also increase healthcare resource utilization [9, 10], which can lead to high health care expenditures for both insurance payers, patients and families. As depression in RA can aggravate disability, an individual may also suffer economic losses due to work inability or even experience economic losses due to missed work days. Although not specific to RA, one study estimated that 6.9 million working-age adults reported arthritis-attributable work limitation [11]. One can speculate that depression can worsen the work limitation because the presence of depression along with any chronic physical condition more than doubles the likelihood of work absenteeism as compared to the presence of any chronic physical condition without depression [12].

However, to date, no published study in the US has done a comprehensive analysis of the humanistic and economic burden associated with depression among RA patients, particularly among working-age adults. In fact, a recent review highlighted the significant knowledge gap in estimating the disease burden of depression in adults with arthritis [4]. Although there has been a handful of studies on the association between depression and HRQoL among adults with RA, most of these studies have been conducted outside the US [13, 14] or only among women in a specific setting [15]. One US study used a cross-sectional design and examined the relationship between depression and disability, HRQoL in the US with data from the 2011 Behavioral Risk Factor Surveillance System [16]. However, this study included all forms of arthritis and did not focus on RA. Again, only one study using 2006 commercial claims data in the US found that RA patients with depression had a significantly higher adjusted annual healthcare costs as compared to RA patients without depression ($12,225 versus $11,404) [9]. However, this study was based on commercially insured RA patients and may not be representative of the US national population. Furthermore, this commercial insurance data did not include certain patient characteristics which are important confounders of healthcare costs such as race, education, and income level.

Therefore, the objective of this study is to examine the incremental burden of depression on the clinical, humanistic, and economic outcomes among working-age adults with RA.

2. Methods

2.1. Study Design

A retrospective cross-sectional study design with data from a nationally representative sample of working-age adults (18–64 years) was used.

2.2. Data Source

We used data from the Medical Expenditure Panel Survey (MEPS), an annual household survey of the noninstitutionalized civilian population in the US. Information on demographic characteristics, medical conditions, health status, utilization of health care services, charges and payments, access to care, health insurance coverage, income, education, employment, and missed workdays of the participants in the survey were extracted from the household component of MEPS. We pooled four years of data (2009, 2011, 2013, and 2015) to have sufficient sample size and used data from alternate years to avoid including two observations per individual. Furthermore, a question related to the type of arthritis was available in these years. MEPS recommends pooling of data to increase sample size and it is a common practice in published literature with MEPS data [17].

2.3. Study Sample

The study sample (N = 2,662) consisted of working-age (18–64 years) who were diagnosed with RA and who were alive during the study period (2009, 2011, 2013, and 2015) (Figure 1). RA was identified from the priority condition enumeration section. In this section, respondents were queried whether an individual in the household has ever been told by a doctor or another health professional that she/he had arthritis and type of arthritis (RA versus osteoarthritis). We also identified RA from medical condition file with the clinical classification code (202). Medical conditions were reported by the respondents if they sought treatment for the condition, or if the condition resulted in disability, or if the condition was bothersome. The responses were recorded as texts, and these texts were translated into International Classification of Diseases, 9th Edition, Clinical Modification (ICD-9-CM) codes by professional coders. In addition, MEPS data provides clinical classification codes, which are aggregated ICD-9-CM codes into clinically meaningful categories that group similar conditions (Agency for Healthcare Research and Quality).

Figure 1.

Figure 1

Flow diagram of study sample.

2.4. Conceptual Framework

The conceptual framework for this study was adapted from the Andersen's Expanded Behavioral Model which posits that health services utilization and outcomes of an individual are a function of predisposing factors (e.g., age, sex, and race), enabling factors (e.g., marital status, education and poverty status), need factors (e.g., chronic conditions, health status), and personal health practices (e.g., physical activity, obesity, and smoking) [18].

2.5. Measures

2.5.1. Clinical Outcomes

Pain Interference with Normal Activities. Based on a self-administered single-item question, pain interference with normal activities during the past four weeks among the household respondents was measured. The answers were recorded on a 5-point Likert scale during the past 4 weeks. In MEPS, pain was reported on a 5-point scale: (1) not at all, (2) a little bit, (3) moderately, (4) quite a bit, and (5) extremely. For purposes of this study we group pain categories as follows: (1) not at all/little bit; (2) moderate; (3) severe (quite a bit/extremely). Self-reported pain from MEPS has been used in published literature to estimate the cost of pain [19]. There were 42 individuals (5.9%) in the depression group and 140 individuals (6.6%) in the no depression group with missing data on pain inference variable. These individuals were not included in the analysis.

Any Functional Limitations. This variable summarizes whether an individual had any limitations in instrumental activities of daily living (IADL) (e.g., shopping, cooking, using phone, paying bills, taking medications, driving, doing laundry, or going shopping), activities of daily living (ADL) (e.g., bathing, dressing, grooming, mouthcare, toileting, and eating), functional limitations (walking, climbing stairs, grasping objects, reaching overhead, lifting, bending or stooping, or standing for long periods of time), or activity limitations (work, housework, or school).

2.5.2. Humanistic Outcome: Health-Related Quality of Life

HRQoL was measured by the generic Short-Form-12 Version 2 (SF12-V2) summary scores. The SF12-V2 is a generic multipurpose survey with 12 questions, which encompass eight domains (role physical, role emotional, physical function, social function, mental health, vitality, pain, and general health). These questions are designed to provide summary measures of overall HRQoL of an individual. The Mental Component Summary (MCS) score was derived from the responses to the items in the domains: vitality, social functioning, role emotional (limitations in work and daily activities because of emotional problems), and mental health. The Physical Component Summary (PCS) score was derived from the responses to the items in the domains: physical functioning, role physical, bodily pain, and general health. Both MCS and PCS scores ranged from 0 to 100, with higher scores representing better self-reported health and better HRQoL related to mental or physical health [20].

2.5.3. Economic Outcomes: Direct Healthcare Expenditures

Total Healthcare Expenditures. In the MEPS, expenditures are defined as the sum of direct payments for care provided during the year. The direct payments include twelve sources of payment categories such as out-of-pocket by patient or families, Medicare, Medicaid, Private Insurance, Veteran Administration, worker's compensation, and others. Total annual per person healthcare expenditures were calculated as the sum of inpatient, outpatient, emergency, dental, home health, vision, prescription drugs, and other medical supplies. All expenditures were inflation adjusted to 2015 US dollars (USD) using consumer price index for medical services from the bureau of medical services.

Total Out-of-Pocket Spending Burden by Patients and Families. We also estimated the total out-of-pocket spending on healthcare by the respondent and/or family. These included annual deductibles, copayment, and coinsurance for services and payment for services that were not covered by health insurance. We calculated out-of-pocket spending burden as the ratio of out-of-pocket healthcare expenditures to personal income [21], which varied from zero to 100. Based on published literature, we defined spending 10% or more of personal income on health care as high out-of-pocket spending burden [22].

2.5.4. Economic Outcomes: Indirect Healthcare Burden

Unemployment (i.e., Labor Market Outcome). In the MEPS, employment section covers questions about each person's employment or self-employment status. Based on these questions, we classified individuals who were currently unemployed.

Missed work days were measured whether individuals lost a half-day or more from work because of illness, injury, or mental or emotional problems during the year and how many workdays were lost. This was calculated only for employed adults.

Lost wages for each individual were calculated by multiplying missed work days with an average daily wage of each individual. All wages were adjusted to 2015 general consumer inflation rates derived from the bureau of labor statistics.

Key Explanatory Variable

Depression (Yes/No). Depression was identified based on the clinical classification code “657,” which included both depressive disorders and bipolar disorders.

Other Explanatory Variables. Predisposing characteristics were sex (male, female), race/ethnicity (Whites, African-American, and other racial minorities), and age in years (18–39, 40–49, and 50–64). Enabling factors comprised marital status (married, widow, separated/divorced, and never married), family poverty status (not poor, poor), health insurance status (public, private), and usual source of care (yes, no). Need factors included having a chronic condition other than RA from a list of eight conditions (asthma, cancer, chronic obstructive pulmonary disease, diabetes, heart disease, hypertension, stroke, and thyroid), anxiety, perceived physical health status (excellent/very good, good, and fair/poor), and perceived mental health status (excellent/very good, good and fair/poor). Personal health practice factors included obesity (obese and not obese), smoking status (current smoker, others, and missing), and exercise (“yes” and “no” exercise).

2.6. Statistical Analyses

A variety of statistical analyses were used based on the measurement of the outcome variables. The unadjusted relationships between the presence of depression and categorical variables and outcomes (pain interference with activities, employment, and OOP burden) were assessed with chi-square tests. Unadjusted differences in continuous outcomes (PCS, MCS, all-cause healthcare expenditures, and out-of-pocket spending by the patients and their families) by depression were tested with t-tests. Multinomial logistic regression was used to analyze the association between depression and pain-related interference with normal work after adjusting for the predisposing, enabling, need, and external environment characteristics. Logistic regression was used to analyze the association between depression and binary categorical variables (e.g., any limitations, unemployment, and out-of-pocket spending burden) after adjusting for covariates. Adjusted models for continuous outcomes (expenditures, out-of-pocket expenditures, and lost wages) consisted of Generalized Linear Models (GLM). GLM is flexible and can handle categorical outcomes, continuous outcomes, and count-data with the appropriate distribution family and a link function. For count-data (e.g., the number of missed work days) we used negative binomial regression.

Counterfactual Prediction Technique (Recycled Prediction). We used counterfactual recycled prediction, an approach that is gaining attention [23, 24] to estimate excess total healthcare expenditures, prescription expenditures, missed work days, and lost wages attributable to depression among working-age adults with Rheumatoid Arthritis. The recycled prediction technique is a preferred approach because it adjusts for differences in characteristics between the depression and no depression group by creating counterfactual scenarios. In all recycled prediction models, confidence intervals were obtained using 2000 bootstrap replications using the percentile method. To account for the complex design of MEPS, we conducted all analyses using the survey procedures in Statistical Analysis Software (SAS) version 9.3, Cary, NC, USA, and the survey design features with STATA 14. As we pooled four years, to get annualized weighted numbers, we divided the weights by four, recommended by the MEPS investigators [25] and used in the published literature [26].

3. Results

3.1. Description of the Study Sample

Majority of the study sample was female (64%) and white (63%), aged between 50 and 64 years (61%), and had multimorbidity (72%). Only 26% of individuals who perceived themselves having excellent or very good physical health and 44.8% reported having excellent or very good mental health (see Table 1).

Table 1.

Description of study sample. Working-age (18 to 64 years) adults with Rheumatoid Arthritis Medical Expenditure Panel Survey (2009, 2011, 2013, and 2015).

N Weighted N Weighted%
All 2,662 5,719,998 100.0
Gender
 Female 1,826 3,661,958 64.0
 Male 836 2,058,040 36.0
Race/ethnicity
 White 1,061 3,596,249 62.9
 African American 778 989,822 17.3
 Latino 639 780,416 13.6
 Others 184 353,511 6.2
Age in years
 18–39 years 444 956,652 16.7
 40–49 years 609 1,271,670 22.2
 50–59 years 1,080 2,326,292 40.7
 60–64 years 529 1,165,384 20.4
Marital status
 Married 1,287 3,098,420 54.2
 Widow/separated/divorced 845 1,630,180 28.5
 Never married 530 991,398 17.3
Education
 Less than high school 665 1,007,827 17.6
 High school 939 2,043,963 35.7
 More than high school 1,036 2,623,400 45.9
Poverty status
 Poor 740 1,216,767 21.3
 Not poor 675 1,204,168 21.1
 Middle income 708 1,670,010 29.2
 High income 539 1,629,054 28.5
Insurance status
 Private 1,302 3,411,533 59.6
 Public 932 1,580,322 27.6
 Uninsured 428 728,144 12.7
Employment
 Employed 1,309 3,071,100 53.7
 Not employed 1,352 2,647,283 46.3
Region
 Northeast 383 984,779 17.2
 Midwest 523 1,264,228 22.1
 South 1,190 2,454,395 42.9
 West 566 1,016,597 17.8
Perceived physical health
 Excellent/very good 607 1,488,614 26.0
 Good 871 2,001,187 35.0
 Fair/poor 1,184 2,230,197 39.0
Perceived mental health
 Excellent/very good 607 1,488,614 26.0
 Good 871 2,001,187 35.0
 Fair/poor 1184 2,230,197 39.0
Multimorbidity
 RA only 716 1,605,886 28.1
 Multimorbidity 1,946 4,114,112 71.9
Anxiety
 Yes 494 1,134,341 19.8
 No 2,168 4,585,657 80.2
Obesity
 Obese 1,218 2,521,340 44.1
 Not obese 1,392 3,084,702 53.9
Smoking status
 Current smoker 698 1,567,457 27.4
 Others 1,755 3,729,925 65.2
 Missing 209 422,616 7.4
Exercise
 Yes 1,077 2,364,802 41.3
 No 1,568 3,321,567 58.1

Note. Based on 2,662 adults with Rheumatoid Arthritis, aged between 18 and 64 years, who were alive during the calendar year. Missing data for the variables, education, obesity, smoking, and exercise, are not presented. Weighted N and percentages were derived by dividing the person weights by the number of years pooled.

Overall, 25.8% of adults with RA reported depression (Table 2). We observed significant differences in the rate of depression by predisposing, enabling, need factors, and personal health practices except for age, education, and region. For example, female adults with RA reported a significantly higher rate of depression than their male counterparts (29.6% versus 19.1%). The higher rate of depression was also observed among individuals with multimorbidity (29.1% versus 17.4%). A higher percentage of those who perceived themselves to be poor/fair physical health reported depression compared to those in excellent or very good health (38.0% versus 12.4%).

Table 2.

Description of study sample by depression among working-age (18–64 years) adults with Rheumatoid Arthritis Medical Expenditure Panel Survey (2009, 2011, 2013, and 2015).

RA with depression RA without depression Sig
N Wt. N Wt. Row% N Wt. N Wt. Row%
All 647 369,136 2,015 1,060,864

Gender ∗∗∗
 Female 502 270,895 29.6 1,324 644,595 70.4
 Male 145 98,241 19.1 691 416,269 80.9
Race/ethnicity ∗∗∗
 White 328 264,578 29.4 733 634,485 70.6
 African American 157 45,643 18.4 621 201,813 81.6
 Latino 127 40,938 21 512 154,166 79
 Others 35 17,977 20.3 149 70,400 79.7
Age in years
 18–39 years 98 58,925 24.6 346 180,238 75.4
 40–49 years 149 82,063 25.8 460 235,855 74.2
 50–59 years 281 156,442 26.9 799 425,131 73.1
 60–64 years 119 71,706 24.6 410 219,640 75.4
Marital status ∗∗∗
 Married 248 160,488 20.7 1,039 614,118 79.3
 Widow/separated/divorced 259 139,902 34.3 586 267,643 65.7
 Never married 140 68,746 27.7 390 179,104 72.3
Education
 Less than high school 170 65,953 26.2 495 186,004 73.8
 High school 232 138,615 27.1 707 372,376 72.9
 Missing 4 2,236 20 18 8,966 80
Poverty status ∗∗∗
 Poor 236 103,612 34.1 504 200,580 65.9
 Not poor 185 88,172 29.3 490 212,870 70.7
 Middle income 141 101,112 24.2 567 316,391 75.8
 High income 85 76,241 18.7 454 331,023 81.3
Insurance status ∗∗∗
 Private 235 183,245 21.5 1,067 669,638 78.5
 Public 345 153,607 38.9 587 241,474 61.1
 Uninsured 67 32,284 17.7 361 149,752 82.3
Employment ∗∗∗
 Employed 195 132,391 17.2 1,114 635,384 82.8
 Not employed 452 236,745 35.8 900 425,076 64.2
Region
 Northeast 89 50,671 20.6 294 195,524 79.4
 Midwest 157 93,289 29.5 366 222,768 70.5
 South 271 161,001 26.2 919 452,598 73.8
 West 130 64,175 25.3 436 189,975 74.7
Perceived physical health status ∗∗∗
 Excellent/very good 72 46,019 12.4 535 326,135 87.6
 Good 165 110,972 22.2 706 389,325 77.8
 Fair/poor 410 212,145 38 774 345,405 62
Perceived mental health status ∗∗∗
 Excellent/very good 113 74,855 11.7 995 565,345 88.3
 Good 207 122,356 25.1 730 365,098 74.9
 Fair/poor 327 171,925 56.9 290 130,422 43.1
Multimorbidity ∗∗∗
 RA only 110 69,703 17.4 606 331,768 82.6
 Multimorbidity 537 299,433 29.1 1,409 729,096 70.9
Anxiety ∗∗∗
 Yes 259 150,809 53.2 235 132,776 46.8
 No 388 218,327 19 1,780 928,088 81
Obesity ∗∗
 Obese 353 190,757 30.3 865 439,579 69.7
 Not obese 287 172,382 22.4 1,105 598,794 77.6
Smoking status ∗∗∗
 Current smoker 250 142,876 36.5 448 248,988 63.5
 Others 355 204,588 21.9 1,400 727,893 78.1
Exercise ∗∗∗
 Yes 190 106,306 18 887 484,895 82
 No exercise 454 259,932 31.3 1,114 570,460 68.7

Note. Based on 2,662 adults with Rheumatoid Arthritis aged between 18 to 64 years, who were alive during the calendar year. Missing data for the variables, education, obesity, smoking, and exercise, are not presented. Asterisks represent significant group differences by the presence of depression based on chi-square tests. Weighted N and percentages were derived by dividing the person weights by the number of years pooled; Wt.: weighted; ∗∗∗p < .001; .001 ≤ ∗∗p < .01.

3.2. Clinical Outcomes

3.2.1. Pain Interference with Normal Activities

A higher percentage of adults with RA and depression reported severe pain interfering with work or other normal activities compared to those with RA and no depression (54.8% versus 30.8%) (Table 3). After adjusting for predisposing, enabling, need, personal health practices, and external environment factors, and adults with depression were 2.2 times as likely to report severe pain interference with normal work activities than those without depression (AOR = 2.22; 95% CI = 1.55, 3.18) (Table 3).

Table 3.

Clinical outcome associated with depression among working-age adults with Rheumatoid Arthritis Medical Expenditure Panel Survey (2009, 2011, 2013, and 2015).

RA + depression RA and no depression Sig
N Wt.
col%
N Wt.
col%
All 605 1,875

Pain interference with daily activity ∗∗∗
 Mild/none 155 29.8 918 51.9
 Moderate 92 15.4 317 17.3
 Severe (extreme/quite a lot) 358 54.8 640 30.8
Limitations
 Any functional limitations 528 79.0 1,026 51.1 ∗∗∗

Adjusted odds ratio and 95% CI for depression from multinomial logistic regression on pain interference with normal activity
AOR 95% CI Sig

Pain interference with daily activity
 Mild/none (reference group)
 Moderate 1.37 [0.91,2.06]
 Severe 2.22 [1.55,3.18] ∗∗∗

Adjusted odds ratio and 95% CI for depression from logistic regression on limitations
AOR 95% CI Sig

Limitations
Any functional limitations 2.24 [1.62,3.10] ∗∗∗

Note. Based on 2,662 adults with Rheumatoid Arthritis aged between 18 and 64 years, who were alive during the calendar year. Adjusted multinomial logistic regression controlled sex, race/ethnicity, age, region, marital status, education, family poverty status, health insurance, physical health status, mental health status, anxiety, multimorbidity, obesity, physical activity, and smoking. Asterisks represent significant group differences by the presence of depression; ∗∗∗p < .001; ADL: activities of daily living; Col: column; IADL: instrumental activities of daily living; Wt.: weighted.

3.2.2. Any Functional Limitations

A significantly higher percentage of adults with RA and depression reported any functional limitations compared to those with RA and no depression (79% versus 51.1%) (Table 3). After adjusting for covariates adults with RA and depression were more than 2 times as likely to report any functional limitations (AOR = 2.24; 95% CI = 1.62, 3.10) (Table 3).

3.3. Humanistic Outcomes

Adults with RA and depression reported significantly lower HRQoL scores in both Physical Component Summary score (35.1 versus 40.2, p < .001) and Mental Component Summary score (37.2 versus 48.7, p < .001) compared to adults with RA without depression (Table 4). In adjusted analyses, a significant difference was observed only in the mental domain of the HRQoL; the presence of depression was associated with a decrement of 8.72 in MCS scores (Table 4). The counterfactual predictions yielded similar differences in MCS (37.19 in adults with depression versus 45.91 in adults without depression, p < .001). The relationship between depression and PCS scores became insignificant after adjustment for the presence of multiple chronic conditions.

Table 4.

Humanistic outcomes (health-related quality of measures) by presence of depression among working-age adults with Rheumatoid Arthritis Medical Expenditure Panel Survey (2009, 2011, 2013, and 2015).

RA + depression RA and no depression Sig
Wt. mean SE Wt. mean SE
All N = 647 N = 2,015

Physical component summary score 35.07 0.89 40.18 0.47 ∗∗∗
Mental component summary
score
37.20 0.77 48.74 0.37 ∗∗∗

Fully adjusted model: parameter estimates and standard errors for depression ordinary least squares regression mental component summary score
Beta Standard error Sig

 Depression −8.72 0.81 ∗∗∗
 No depression (reference group)

Fully adjusted model: parameter estimates and standard errors for depression ordinary least squares regression physical component summary score
Beta Standard error Sig

 Depression −1.29 0.81
 No depression (reference group)

Note. Based on 2,662 adults with Rheumatoid Arthritis aged between 18 and 64 years, who were alive during the calendar year. Asterisks represent significant group differences by the presence of depression. The ordinary least squares regressions controlled for the following variables: sex, race/ethnicity, age, region, marital status, education, family poverty status, health insurance, anxiety, multimorbidity, obesity, physical activity, and smoking; SE: standard error; Wt.: weighted; ∗∗∗p < .001.

3.4. Economic Outcomes

3.4.1. Direct Total Healthcare Expenditures

In unadjusted analysis, adults with RA and depression had significantly higher annual healthcare expenditures ($17,941 versus $10,064 p < .001). In the adjusted GLM with gamma distribution and log-link, we found that depression was associated with greater total healthcare expenditures compared to those without depression (Beta = 0.34, SE = 0.08). When converted to original dollars this represented $14,752 for those with depression and $10,541 for those without depression (Table 5). Estimates from counter-factual recycled prediction revealed that depression was associated with an excess of $4,212 total healthcare expenditures with 95% CI = $4,114, $4,318.

Table 5.

Economic outcomes by presence of depression among working-age adults with Rheumatoid Arthritis Medical Expenditure Panel Survey (2009, 2011, 2013, and 2015).

RA + depression RA and no depression Sig
Wt. mean SE Wt. mean SE
All N = 647 N = 2,015

Total healthcare expenditures (2015 $) 17,941 1489 10,064 574 ∗∗∗
Total out-of-pocket spending by patients/families (2015 $) $1,443 135 $1,052 73 ∗∗∗

Adjusted total direct healthcare expenditures of depression from generalized linear models with gamma distribution and log link
Wt. mean 95% CI Wt. mean 95% CI Sig

∗∗∗
Total healthcare expenditures (2015 $) 14,752 (14,411–15,125) 10,541 (10,206–10,806)
Total out-of-pocket spending by patients/families (2015 $) 1,232 (1,202–1265) 979 (955–1,005) ∗∗∗

Incremental total direct healthcare expenditures of depression from counterfactual recycled prediction
Wt. mean 95% CI

Total healthcare expenditures (2015 $) 4,212 (4,114, 4318) ∗∗∗
Total out-of-pocket spending by patients/their families (2015 $) 253 (247–260) ∗∗∗

High out-of-pocket spending burden (>10% income spent on healthcare)
RA + depression RA and no depression
N Wt. col% N Wt. col%

High out-of-pocket spending burden 192 30.7 424 21.3 ∗∗∗

Fully adjusted model: adjusted odds ratio (AOR) and 95% confidence intervals (CI) of Depression from logistic regression on high out-of-pocket burden
AOR 95% CI Sig

Depression 1.34 [1.01,1.79] ∗∗
No depression (reference)

Unemployment among working-age adults
RA + depression RA and no depression
N Wt. col% N Wt. col%

Unemployed 452 64.1 900 40.1 ∗∗∗

Fully adjusted model: adjusted odds ratio (AOR) and 95% confidence intervals (CI) of depression from logistic regression on unemployment
AOR 95% CI Sig

Depression 1.55 [1.14, 2.10] ∗∗∗
No depression (reference)

Fully adjusted models: total productivity losses by depression from negative binomial regression on missed work Days
Wt. mean 95% CI Wt. mean 95% CI Sig

∗∗∗
Number of missed work days 9.0 (8.7–9.4) 6.0 (5.7–6.2)
Lost wages 853 (833–873) 571 (558–584) ∗∗∗

Incremental total productivity losses associated with depression from counterfactual recycled prediction
Wt. mean 95% CI

Number of missed work days 3.1 (2.9–3.2)
Lost wages 282 (276–289)

Note. Based on 2,662 adults with Rheumatoid Arthritis aged between 18 and 64 years, who were alive during the calendar year. Asterisks represent significant group differences by the presence of depression. The adjusted models squares regressions controlled for the following variables: sex, race/ethnicity, age, region, marital status, education, family poverty status, health insurance, physical health, mental health status, anxiety, multimorbidity, obesity, physical activity, and smoking. Missed work days and lost wages were estimated only for those who were employed; ∗∗∗p < .001; .001 ≤ ∗∗p < .01; .01 ≤ p < .05.

In unadjusted analysis, patients/families in the RA + depression group spent significantly higher amounts out-of-pocket on health care compared to the RA + no depression group ($1,443 versus $1,052, p < .001). In the adjusted GLM with gamma distribution and log-link, we found that depression was associated with greater total out-of-pocket healthcare spending compared to those without depression (Beta = 0.23, SE = 0.06). When converted to original dollars this represented $1,232 for those with depression and $979 for those without depression (Table 5). Estimates from counter-factual recycled prediction revealed that depression was associated with an excess of $253 with 95% CI = $247, 260.

When high out-of-pocket spending burden was measured as spending greater than 10% of income on healthcare, we found that 30.7% of adults with depression and 21.3% of adults without depression had high out-of-pocket spending burden. After adjusting for other factors, adults with depression were significantly more likely to have high out-of-pocket spending burden (AOR = 1.34; 95% CI = 1.01, 1.79).

3.4.2. Indirect Economic Burden

Labor Market Outcome (Unemployment), Missed Work Days, and Lost Wages. Presence of depression was significantly associated with unemployment among adults with RA; 64.1% of adults with depression were unemployed compared to 40.1% adults without depression. Even after controlling for other factors mentioned in the methods section, adults with RA and depression were 1.55 times as likely as those without depression to be unemployed (AOR = 1.55; 95% CI = 1.14, 2.10). Among employed adults, those with depression had significantly higher number of missed work days annually (9 versus 6, p < .05) and higher lost wages ($813 versus $571, p < .05) due to missed work (Table 5). We obtained similar results with counterfactual recycled predictions.

4. Discussion

In this study using a nationally representative sample of community-dwelling US adults, one in four working-age adults with RA reported depression. This rate is considerably higher compared to the 6.8% rate of depression in the general population in the US [27] and higher than the pooled depression rate of 16.8% reported by Matcham and colleagues in a meta-analysis of 72 studies that included 13,189 RA patients [5]. The same meta-analysis also reported the presence of depressive symptoms in 38.8% of RA patients measured using Patient Health Questionnaire (PHQ-9) and 34.2% of RA patients measured using Hospital Anxiety and Depression Scale (HADS) [5]. Therefore, the differences in the rate of depression in RA patients can be explained by the differences in the instruments used to identify depression.

Our study findings indicated the substantial additional clinical burden imposed by depression in working-age adults with RA. These findings have implications for comanagement of depression and RA. Although not specific to RA, a randomized clinical trial of 1,001 patients with concurrent depression and arthritis and seeking care from 18 primary care clinics [28] suggested that collaborative depression care not only reduced depressive symptoms but also improved arthritis related outcomes, such as decreasing pain and functional limitations. There is some evidence that disease-modifying drugs used to treat RA can have spill-over effects in reducing depressive symptoms. For example, depression levels decreased significantly following commencement and continuity of rituximab, a B cell-directed therapy, among individuals with RA [29]. Therefore, future studies need to systematically evaluate whether antirheumatic treatment among individuals with RA can help alleviate depressive symptoms.

We also observed significant decrements in HRQoL measures, specifically the MCS scores. This is not surprising; however, it is important given the strong association between patient-reported outcomes and disease activity [30]. It has also been suggested that patient-reported outcomes such as the HRQoL and other measures in clinical trials and routine clinical practice may shed light on variations in treatment response as well as the burden of disease among RA adults [30, 31]. Our findings suggest that collecting patient-reported HRQoL can be critical in assessing disease burden that may not be captured by clinical assessment alone [30].

Depression in working-age adults with RA was associated with substantial direct and indirect economic burden. For example, the presence of depression more than doubled the annual per person total healthcare costs, a number of missed work days, and lost wages due to missed work days, even after controlling for predisposing factors, enabling characteristics, need factors, and personal health care practices. Although published evidence on the incremental economic impact of depression in RA is limited [9], our findings which are consistent with studies assessing the burden of depression on other chronic illnesses such as diabetes, cardiovascular disease, and asthma have also reported the synergistic effect of depression in increasing the economic burden among individuals with chronic conditions [12, 32].

Our findings on the economic burden of depression in RA patients have important implications for the payers as it highlights an opportunity for reducing expenditures in RA patients by increasing efforts towards screening and effectively treating depression in RA patients. Potential strategies could be improving the integration of mental health services with rheumatology practice and facilitating mental health training for rheumatologists. Future studies need to explore whether treatment for depression provides an opportunity to reduce direct healthcare expenditures associated with depression in RA patients.

The study findings have important implications for the employers because depression costs US employers more than $31 billion annually due to missed work and decreased work performance [33]. One study done in the US reported that depression leads to the highest reduction in work performance and the highest employer burden relative to any other chronic conditions [34]. Strategies that employers may adopt to improve mental health in employees include organizing workplace health promotion programs and stress management projects, which have shown the benefits of prevention and management of depression in workplace [35, 36].

To the best of our knowledge, this is the first population-based study that comprehensively examined the excess clinical, humanistic, and economic burden of depression in working-age adults with RA. Other strengths of this study include the use of nationally representative survey, adjustment of a comprehensive list of confounders such as predisposing factors, enabling factors, need factors, and personal health care practices and the use of robust statistical techniques such as GLM, and recycled prediction in estimating the incremental costs and missed workdays.

However, the findings of this study should be interpreted considering its potential limitations. First, we did not control for the severity and duration of RA and depression as MEPS does not contain this information. These factors can be important confounders of both healthcare costs and work absence. Second, we have measured productivity loss as missed work days and did not consider other kinds of productivity loss such as reduced productivity while at work (presenteeism) and loss of employment.

Our findings would provide valuable insights to payers and other decision-makers to better understand the economic impact of comorbid depression on working RA patients from US societal perspective. It is well-documented that depression in RA patients is often underrecognized and undertreated in routine clinical practice [37, 38]. Therefore, our study underscores the need for incorporating depression screening and management in the routine clinical management of RA in order to offset the substantial incremental costs associated with depression. Published evidence has well documented that depression is a treatable condition. However, it is still not clear whether depression treatment is equally effective in RA patients as compared to those with depression without RA [39]. Future studies need to assess the potential cost reductions that can be achieved through early detection and more aggressive treatment of depression in RA patients.

Acknowledgments

The project was supported by the National Institute of General Medical Sciences, 2U54GM104942.

Disclosure

The content is solely the responsibility of the authors and does not necessarily represent the views/opinions of any organization.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

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