Session Information
Session Type: Abstract Submissions (ARHP)
Background/Purpose
Having a first-degree relative (FDR) with RA increases personal RA risk by four-fold. Other RA risk factors include demographics, genetics, auto-antibodies, and behaviors. We aimed to develop a personalized RA risk tool incorporating these risk factors, suitable for use in RA education trials. We explored changes in self-perceived RA risk and RA knowledge after personalized RA risk education among a group at increased RA risk due to having a relative affected with RA.
Methods
We conducted a pilot study on RA self-perceived risk, knowledge, and attitudes among FDRs recruited at a large academic hospital. Eligible participants had a FDR with RA. We developed a web-based interactive tool, the Personalized Risk Estimator for RA (PRE-RA), which provided RA education and calculated lifetime RA risk based on demographics, genetics (HLA shared epitope), auto-antibodies (RF and ACPA), and behaviors (smoking, overweight/obesity, low fish intake, and dental health). RA knowledge and attitudes were assessed before and 6 weeks after the intervention: PRE-RA and health education. RA risk factor knowledge was evaluated by whether subjects agreed that an established risk factor, supported by literature, increased RA risk. An RA knowledge index was calculated by the total number of established factors agreed to increase RA risk. Self-perceived lifetime RA risk before and after the intervention was compared to the PRE-RAcalculated lifetime RA risk using Wilcoxon rank-sum test. RA knowledge and attitudes before and after intervention were compared by Fisher’s exact or Wilcoxon rank-sum tests.
Results
A total of 37 subjects enrolled in the study and 14 completed the PRE-RA tool with health education. Median age was 44 years (range 20-70) and 76% were female. Using demographics, behaviors, genetics, and auto-antibodies, the median personalized lifetime calculated RA risk was 5% (range 1-56, mean 12.4, SD 14.7; Table) and was significantly lower than self-perceived risk at baseline (median 50%, range 0-85, mean 38.6, SD 23.7; p=0.0002). After intervention, self-perceived risk approached the calculated PRE-RA risk but remained significantly higher (median 14%, range 1-80, mean 25.1, SD 26.5; p=0.04). RA knowledge index significantly improved after the PRE-RA tool (median 8, mean 8.6, SD 0.5) compared to baseline (median 6, mean 5.4, SD 1.6; p<0.0001). Only 20% agreed that smoking was a risk factor for RA at baseline, but 100% agreed after the intervention (p<0.0001).
Conclusion
We developed an interactive RA risk education tool, PRE-RA, personalized to demographics, behaviors, genetics, and auto-antibodies suitable for use in RA risk education trials. Subjects in our study had high self-perceived RA risk, compared to calculated risk, that became more accurate after personalized RA risk education. Knowledge of RA risk factors was low prior to intervention and significantly increased after the PRE-RA tool and health education.
Table. RA risk self-perception, knowledge, and attitudes at baseline and after the Personalized Risk Estimator for RA (PRE-RA) tool and health education among RA first-degree relatives. |
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Self-perceived vs. calculated lifetime RA risk |
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|
Self-perceived lifetime RA risk |
Calculated PRE-RA tool lifetime RA risk |
P value |
Baseline lifetime % RA risk, median (range) |
50 (0-85) |
5 (1-56) |
0.0002 |
Post-intervention lifetime % RA risk, median (range) |
14 (1-80)* |
5 (1-56) |
0.04 |
Baseline vs. 6-weeks after intervention |
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|
Baseline (n = 37) |
After PRE-RAtool and health education (n = 14) |
P value |
Lifetime % RA risk, median (range) |
50 (0-85) |
14 (1-80) |
0.043 |
Smoking is a risk factor for RA, % agree |
20% |
100% |
<0.0001 |
Diet is a risk factor for RA, % agree |
53% |
67% |
0.68 |
Dental health is a risk factor for RA, % agree |
7% |
67% |
0.003 |
Obesity is a risk factor for RA, % agree |
40% |
89% |
0.033 |
RA knowledge index, median (range) |
6 (3-8) |
8 (7-9) |
<0.0001 |
>45% lifetime RA risk for average person, % agree |
16% |
0% |
0.17 |
18% lifetime risk of RA is low or very low, % agree |
51% |
36% |
0.36 |
*A total of 14 subjects provided self-perceived risk after the PRE-RA tool and health education. |
Disclosure:
J. A. Sparks,
None;
M. D. Iversen,
Pfizer Inc,
2;
R. Miller Kroouze,
None;
N. A. Triedman,
None;
T. G. Mahmoud,
None;
S. S. Kalia,
None;
M. L. Atkinson,
None;
R. C. Green,
None;
E. W. Karlson,
None.
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