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Abstract Number: 1182

The Disproportionate High Risk of Re-Fracture after Osteoporotic Treatment in Patients with Autoimmune Diseases

Wen-Nan Huang1, Yi-Ming Chen1, Wei-Ting Hung2, Yu-Wan Liao3 and Yi-Hsing Chen1, 1Division of Allergy, Immunology and Rheumatology, Taichung Veterans General Hospital, Taichung, Taiwan, 2Division of Allergy, Immunology and Rheumatology, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan, 3Taichung Veterans General Hospital, Taichung, Taiwan

Meeting: 2018 ACR/ARHP Annual Meeting

Keywords: autoimmune diseases, fracture risk and osteoporosis

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Session Information

Date: Monday, October 22, 2018

Session Title: Health Services Research Poster II – ACR/ARHP

Session Type: ACR/ARHP Combined Abstract Session

Session Time: 9:00AM-11:00AM

Background/Purpose: Patients with autoimmune diseases are associated with an increased risk of osteoporotic fracture. Anti-osteoporotic treatment could diminish re-fracture rates in post-menopause women. However, treatment failure of anti-osteoporotic medication in patients with autoimmune diseases remained unknown. The aim of study is to investigate the outcome of anti-osteoporotic treatment in patients with autoimmune rheumatic diseases.

Methods: We conducted a retrospective case-control study analyzing hospital database of a tertiary referral center in Taiwan. From January, 2002 to December 2016, subjects with osteoporotic fracture and anti-osteoporotic treatment were enrolled. Diagnosis of rheumatoid arthritis, systemic lupus erythematosus and primary Sjogren¡¦s syndrome were identified using ICD-9-CM and ICD-10-CM codes. Cases with re-fracture were compared with age-, gender-matched controls (1:4) without re-fracture. Re-fracture incidences were compared among anti-osteoporotic drugs and autoimmune diseases.

Results: In total, 9,384 fracture patients with anti-osteoporotic drugs were indentified; 1,829 patients with autoimmune diseases. Patients receiving teriparatide were older and had lower bone density compared with those receiving bisphosphonates, raloxifene and denosumab, respectively. Participants with previous hip fractures had higher chance of re-fracture compared with their counterparts of previous spine fractures or other fractures. Patients with autoimmune diseases were at higher risk of recurrent fractures (19.3% vs. 10.6%, p<0.001). Moreover, bisphosphonates-treated patients also had higher re-fracture rates compared with those treated with raloxifene, denosumab and teriparatide.

Conclusion: Our results indicated that rheumatic patients were at increased risk of treatment failure in osteoporosis. Adherence of anti-osteoporotic drugs and fall prevention are essential to prevent re-fracture in patients with autoimmune diseases.

Table 1. Demographic data and baseline bone mineral density in patients receiving anti-osteoporotic treatment

Bisphosphonate (n=5853)

Teriparatide (n=916)

Denosumab

(n=1058)

Raloxifene (n=1557)

Total (n=9384)

p value

 

¡@

n

%

n

%

n

%

n

%

n

%

 

Age

72.0

¡Ó11.2

76.4

¡Ó9.5

73.3

¡Ó10.5

71.0

¡Ó10.3

72.4

¡Ó10.9

<0.001**

 

Gender

<0.001**

 

Female

4260

(72.8%)

760

(83.0%)

902

(85.3%)

1554

(99.8%)

7476

(79.7%)

 

Male

1593

(27.2%)

156

(17.0%)

156

(14.7%)

3

(0.2%)

1908

(20.3%)

 

First fracture

<0.001**

 

Osteoporotic fracture

2560

(43.7%)

226

(24.7%)

347

(32.8%)

711

(45.7%)

3844

(41.0%)

 

Spine fracture

2555

(43.7%)

603

(65.8%)

513

(48.5%)

644

(41.4%)

4315

(46.0%)

 

Hip fracture

510

(8.7%)

63

(6.9%)

120

(11.3%)

140

(9.0%)

833

(8.9%)

 

Others

228

(3.9%)

24

(2.6%)

78

(7.4%)

62

(4.0%)

392

(4.2%)

 

RA

445

(7.6%)

40

(4.4%)

52

(4.9%)

60

(3.9%)

597

(6.4%)

<0.001**

 

SLE

309

(5.3%)

31

(3.4%)

31

(2.9%)

44

(2.8%)

415

(4.4%)

<0.001**

 

pSS

615

(10.5%)

56

(6.1%)

63

(6.0%)

83

(5.3%)

817

(8.7%)

<0.001**

 

Subspecialties

<0.001**

 

Orthopedics

2972

(50.8%)

416

(45.4%)

564

(53.3%)

1022

(65.6%)

4974

(53.0%)

 

Neurosurgery

1275

(21.8%)

367

(40.1%)

200

(18.9%)

308

(19.8%)

2150

(22.9%)

 

Rheumatology

862

(14.7%)

90

(9.8%)

106

(10.0%)

85

(5.5%)

1143

(12.2%)

 

Others

744

(12.7%)

43

(4.7%)

188

(17.8%)

142

(9.1%)

1117

(11.9%)

 

Baseline

 

Femoral neck BMD (g/cm2)

0.6

¡Ó0.1

0.6

¡Ó0.1

0.6

¡Ó0.1

0.6

¡Ó0.1

0.6

¡Ó0.1

<0.001**

 

Lumbar spine BMD (g/cm2)

0.9

¡Ó0.2

0.8

¡Ó0.2

0.9

¡Ó0.2

0.8

¡Ó0.2

0.9

¡Ó0.2

<0.001**

 

T-score

-2.8

¡Ó0.9

-3.4

¡Ó0.9

-2.8

¡Ó0.8

-2.8

¡Ó0.9

-2.9

¡Ó0.9

<0.001**

 

Chi-Square test. Kruskal Wallis test.*p<0.05, **p<0.01.

Continuous data were expressed mean¡ÓSD.

Categorical data were expressed number and percentage.


Table 2. Comparisons of demographic data, concomitant autoimmune diseases and anti-osteoporotic treatment in patients with and without re-fracture

¡@

Without re-fracture (n=3256)

With re-fracture (n=814)

Total (n=4070)

p value

 

Age

74.1

¡Ó10.0

73.7

¡Ó10.2

74.0

¡Ó10.0

0.628

Gender

1.000

Female

2564

(78.7%)

641

(78.7%)

3205

(78.7%)

Male

692

(21.3%)

173

(21.3%)

865

(21.3%)

First fracture

0.008**

Osteoporotic fracture

1466

(45.0%)

386

(47.4%)

1852

(45.5%)

Spine fracture

1348

(41.4%)

290

(35.6%)

1638

(40.2%)

Hip fracture

284

(8.7%)

92

(11.3%)

376

(9.2%)

Others

158

(4.9%)

46

(5.7%)

204

(5.0%)

Autoimmune disease

345

(10.6%)

157

(19.3%)

502

(12.3%)

<0.001**

RA

194

(6.0%)

102

(12.5%)

296

(7.3%)

<0.001**

SLE

123

(3.8%)

78

(9.6%)

201

(4.9%)

<0.001**

pSS

274

(8.4%)

124

(15.2%)

398

(9.8%)

<0.001**

Anti-osteoporotic treatment

<0.001**

Bisphosphonate

2045

(62.8%)

578

(71.0%)

2623

(64.4%)

Teriparatide

305

(9.4%)

47

(5.8%)

352

(8.6%)

Denosumab

385

(11.8%)

46

(5.7%)

431

(10.6%)

Raloxifene

521

(16.0%)

143

(17.6%)

664

(16.3%)

Subspecialties

0.001**

Orthopedics

1803

(55.4%)

431

(52.9%)

2234

(54.9%)

Neurosurgery

650

(20.0%)

141

(17.3%)

791

(19.4%)

Rheumatology

384

(11.8%)

139

(17.1%)

523

(12.9%)

Others

419

(12.9%)

103

(12.7%)

522

(12.8%)

Baseline lab data

Creatinine

1.1

¡Ó0.8

1.1

¡Ó0.9

1.1

¡Ó0.9

0.008**

ALT

23.5

¡Ó26.3

24.1

¡Ó22.9

23.6

¡Ó25.7

0.083

Hgb (n=2536)

12.1

¡Ó1.7

11.9

¡Ó1.9

12.1

¡Ó1.7

0.006**

Femoral neck BMD (g/cm2)

0.6

¡Ó0.1

0.6

¡Ó0.1

0.6

¡Ó0.1

0.017*

Lumbar spine BMD (g/cm2)

0.9

¡Ó0.2

0.9

¡Ó0.2

0.9

¡Ó0.2

0.438

T-score

-2.8

¡Ó0.9

-2.9

¡Ó1.0

-2.8

¡Ó0.9

0.227

Chi-Square test. Kruskal Wallis test. *p<0.05, **p<0.01.

 

Continuous data were expressed mean¡ÓSD.

 

Categorical data were expressed number and percentage.

 


Disclosure: W. N. Huang, None; Y. M. Chen, None; W. T. Hung, None; Y. W. Liao, None; Y. H. Chen, None.

To cite this abstract in AMA style:

Huang WN, Chen YM, Hung WT, Liao YW, Chen YH. The Disproportionate High Risk of Re-Fracture after Osteoporotic Treatment in Patients with Autoimmune Diseases [abstract]. Arthritis Rheumatol. 2018; 70 (suppl 9). https://acrabstracts.org/abstract/the-disproportionate-high-risk-of-re-fracture-after-osteoporotic-treatment-in-patients-with-autoimmune-diseases/. Accessed April 1, 2023.
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