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Organ damage is a significant issue for patients with systemic lupus erythematosus (SLE) and patients who accrue damage early have a poorer prognosis, with organ damage in the first year being associated with a 3–4-fold increase in 10-year mortality.1
The role of ethnicity and socioeconomic status in the pattern and severity of damage accrual in SLE has been unclear, with few studies examining these areas together. To address this, Kallas and colleagues1 published an article in Journal of Rheumatology, which examines the trajectory of damage accrual overall and in individual organ systems in a group of African American and Caucasian patients with SLE, including an assessment of the impact of specific socioeconomic factors. We are pleased to provide a summary of this article here.
The study included 2,436 patients with SLE divided into two cohorts based on ethnicity from the prospective Hopkins Lupus Cohort, who were classified using the Systemic Lupus International Collaborating Clinics (SLICC) classification criteria or revised American College of Rheumatology (ACR) classification criteria.
The SLICC/ACR damage index (DI) includes 12 organ systems to measure damage, which is defined as “irreversible organ dysfunction, present for 6 months or longer regardless of etiology” and was used to compare the DI between the two groups.
Socioeconomic factors were collected by self-reported patient questionnaires and included years of education, insurance type, and combined family income.
In the overall cohort, 42.9% of patients were African American and 57.1% were Caucasian and the mean age when SLE was diagnosed was 33 years. Patients diagnosed with SLE before the age of 30 years made up 49% of the overall cohort, with 33.6% being diagnosed when aged 30−45 years.
As shown in Table 1, the groups comprising African American and Caucasian patients were well-matched with regards to age, follow-up time since diagnosis, and sex. When looking at socioeconomic markers, African American patients were less likely to have >12 years of education, a household income of >$65,000, or to have private health insurance compared with Caucasian patients.
Table 1. Baseline patient characteristics*
Baseline characteristic, % (unless otherwise stated) |
All |
African American |
Caucasian |
---|---|---|---|
Mean age at SLE diagnosis ± SD, years |
32.7 ± 13.0 |
31.3 ± 12.1 |
33.6 ± 13.5 |
Mean follow-up since SLE diagnosis ± SD, years |
13.4 ± 10.0 |
13.6 ± 10.2 |
13.3 ± 9.8 |
Female |
92 |
93.4 |
91.0 |
Education |
|
|
|
≤12 years |
34 |
40.8 |
28.7 |
>12 years |
66 |
59.2 |
71.3 |
Family income |
|
|
|
<$30,000 |
33 |
49.2 |
20.3 |
$30,000 − <$65,000 |
33 |
28.9 |
35.8 |
≥$65,000 |
24 |
21.8 |
43.9 |
Insurance |
|
|
|
None |
2 |
4.0 |
1.3 |
Medical assistance |
19 |
30.2 |
10.9 |
Private |
78 |
65.8 |
87.8 |
SD, standard deviation; SLE, systemic lupus erythematosus. |
The organ systems that showed a significant difference between the two patient groups in terms of damage accrual are shown in Table 2. Following adjustments for sex, age at diagnosis, years of education, health insurance, and household income, African American patients were shown to have a significantly higher rate of damage accrual compared with Caucasian patients. This was particularly notable in the renal and pulmonary systems and the skin.
On univariate analysis, there was also a significant difference in risk of musculoskeletal and cardiovascular damage, but this was not significant following adjustment for age at diagnosis, sex, and socioeconomic factors.
Table 2. Adjusted and unadjusted rates of damage accrual in African American and Caucasian patients in organ systems*
Type of damage |
Rate of SLICC/ACR DI per year |
Rate ratio |
p value |
Adjusted rate ratio† |
p value |
|
---|---|---|---|---|---|---|
African American |
Caucasian |
|||||
Total |
0.16 |
0.12 |
1.30 |
<0.0001 |
1.14 |
0.010 |
Renal |
0.03 |
0.016 |
1.99 |
<0.0001 |
1.68 |
<0.0001 |
Pulmonary |
0.016 |
0.011 |
1.47 |
0.0006 |
1.38 |
0.0066 |
Cardiovascular |
0.012 |
0.009 |
1.32 |
0.0352 |
1.26 |
0.1023 |
Musculoskeletal |
0.03 |
0.02 |
1.31 |
0.0002 |
1.11 |
0.2086 |
Skin |
0.007 |
0.002 |
4.15 |
<0.0001 |
2.98 (1.83–4.85) |
<0.0001 |
CI, confidence interval; SLICC/ACR DI, Systemic Lupus International Collaborating Clinic/revised American College of Rheumatology damage index. |
The association between individual DI items according to SLICC/ACR is shown in Figure 1 and indicates that African American patients had an increased adjusted rate ratio for the following compared with Caucasian patients at any time during follow-up:
Additionally, there were specific SLICC/ACR DI items that were increased in Caucasian patients, including osteoporosis with fracture or vertebral collapse, bowel infarction, venous thrombosis, and malignancy.
Figure 1. Forest plot showing the SLICC/ACR DI items that were significantly different between ethnic groups*
ACR, American College of Rheumatology; GFR, glomerular filtration rate; SLICC, Systemic Lupus International Collaborating Clinics.
*Data from Kallas, et al.1
†Adjusted for sex, age at diagnosis, years of education, income, and insurance.
Assessing trends in damage accrual over time showed a linear increase for both groups of patients with SLE. Increased mean damage scores for skin and renal, pulmonary, and musculoskeletal systems were observed in African American patients compared with Caucasian patients at any point following SLE diagnosis. The incidence of damage in specific organ systems is shown in Table 3.
Table 3. Incidence of damage in specific organ systems over time*
Incidence, % |
African Americans |
Caucasians |
---|---|---|
5 years after SLE diagnosis |
|
|
Incidence of renal damage |
11 |
6 |
15 years after SLE diagnosis |
|
|
Incidence of renal damage |
21 |
14 |
Incidence of pulmonary damage |
17 |
14 |
Incidence of musculoskeletal damage |
35 |
25 |
Incidence of skin damage |
11 |
3 |
SLE, systemic lupus erythematosus. |
There were certain limitations to the study; socioeconomic factors were considered to be fixed following SLE diagnosis, the individual impact of the three measures of socioeconomic status could not be analyzed individually, and confounding variables, such as disease activity, corticosteroid use, adherence to medication, and obesity, were not accounted for. In addition, this study was predominantly focused on African American and Caucasian patients so its findings cannot be generalized to other ethnicities.
On the other hand, the study had certain strengths. The large cohort of patients from two ethnic groups was followed-up for a mean of 13 years. In addition, the impact of socioeconomic status was assessed with three different measures.
The study showed that African American patients with SLE not only are more likely to experience damage accrual in their renal, pulmonary, or skin systems but that it occurs at a faster rate compared with Caucasian patients even after adjusting for socioeconomic factors. Therefore, in this study, ethnicity was a significant factor in organ damage severity, rate of accrual, and the organ systems affected in patients with SLE. Both Caucasian and African American patients showed a linear increase in damage over time, which shows the need for interventions to protect against organ damage.
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