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Abstract Number: 2395

Body Composition, Strength, and Function in Elderly Patients with Giant Cell Arteritis

Rebecca L. Manno1, Allan C. Gelber2, Philip Seo3, Stuart M. Levine4, Sharon R. Ghazarian5, Po-Han Chen6, Kerry J. Stewart7, Jeffrey Metter8, Luigi Ferrucci8 and Kevin R. Fontaine9, 1Division of Rheumatology, Johns Hopkins University, Baltimore, MD, 2Medicine/ Rheumatology, Johns Hopkins University, Baltimore, MD, 3Rheumatology Division, Johns Hopkins Vasculitis Center, Johns Hopkins University, Baltimore, MD, 4Medicine/Rheumatology, Johns Hopkins University, Baltimore, MD, 5Bayview Biostatistics, Epidemiology and Data Management (BEAD) Core, Johns Hopkins University, Johns Hopkins University, Baltimore, MD, 6Bayview Biostatistics, Epidemiology and Data Management (BEAD) Core, Johns Hopkins University, Baltimore, MD, 7Clinical and Research Exercise Physiology, Johns Hopkins University, Baltimore, MD, 8National Institutes of Health, National Institute on Aging, Baltimore, MD, 9Health Behavior, The University of Alabama at Birmingham, Birmingham, AL

Meeting: 2012 ACR/ARHP Annual Meeting

Keywords: body mass, functional status and giant cell arteritis

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Session Information

Title: Vasculitis

Session Type: Abstract Submissions (ACR)

Background/Purpose : Loss of muscle and strength typically occur with advanced age. Chronic inflammatory diseases, such as rheumatoid arthritis, have reported similar deficits. Giant cell arteritis (GCA) is an inflammatory systemic vasculitis that occurs almost exclusively in the elderly. We sought to determine the body composition, strength, and functional disability in a cross-sectional sample of GCA patients (pts) and compare these parameters to age-matched community dwelling non-GCA controls. 

Methods : Pts were recruited from a tertiary academic center. Body composition was evaluated by dual energy x-ray absorptiometry (DEXA, GE Lunar Prodigy Software V13); strength was assessed by hand grip dynamometry and lower extremity isokinetic testing (Biodex System 3 dynamometer); and functional disability by the short physical performance battery (SPPB). The SPPB includes: chair stands, semitandem, tandem, one-leg stand, and gait speed (6 meter walk). GCA pts were matched (1:2 ratio) by age (within 1 year), gender, and race to eligible controls randomly selected from the Baltimore Longitudinal Study of Aging (BLSA). The BLSA prospectively follows a cohort of healthy volunteers who undergo comprehensive evaluation every 1-2 years. Continuous and categorical variables were compared using student’s t-test and chi-square analyses respectively.

Results : GCA pts (N=18) had a mean ± SD age of 74 ± 7 yrs (range 59-86). They were mostly female (83%), white (83%) and had a positive temporal artery biopsy (89%). Mean disease duration was 2.7 ± 4.1 yrs (range 0.1-16); 7 (39%) were diagnosed >2 years prior to their study visit. Most (78%) were on daily prednisone (11 ± 13 mg/d) with a mean duration of steroid exposure at the study visit of 11 ± 13 months. GCA pts were significantly weaker on all measures of strength compared to BLSA controls (Table 1). GCA pts also had marked slowness as indicated by longer time to complete chair stands and slower gait speed. Body composition was similar between the two groups without a corresponding decrease in lean mass among the GCA group despite their decreased strength.

Conclusion :  GCA pts in this small cross-sectional study were significantly weaker and slower than age-matched controls in the absence of significant differences in body composition. Slow gait speed (<0.8 m/s) is associated with disability, morbidity, and mortality among elderly adults. The preservation of lean mass in elderly GCA pts, in the presence of clinically significant weakness, suggests that impairment/dysfunction in muscle quality rather than muscle quantity may be the culprit. Prednisone use may be a significant contributor to weakness and slowness in elderly GCA pts. However, prednisone is unavoidable in the treatment of this potentially catastrophic illness and future investigation should focus on methods to improve strength and function in GCA pts regardless of their need for steroid therapy.

 Table 1.

 

GCA

N=18

BLSA

N=36

p-value

Age, mean ± SD (years)

75 ± 7

74 ± 7

0.672

 

Gender (% women)

83

78

0.633

 

 

 

 

Race (% Caucasian)

83

83

1.000

 

 

 

 

Strength Measures

 

 

 

Grip strength (kg)

21 ± 6

27 ± 9

0.015

 

 

 

 

Leg extension 180d/s peak torque (Nm)

 

 

 

            Left quadriceps

46 ± 17

89 ± 2 (n=23)

<0.001

            Right quadriceps

49 ± 20

69 ± 16 (n=31)

0.001

 

 

 

 

Leg flexion 180d/s peak torque (Nm)

 

 

 

            Left hamstrings

21 ± 10

66 ± 22 (n=23)

<0.001

            Right hamstrings

23 ± 10

49 ± 15 (n=31)

<0.001

Functional Measures (Short Physical Performance Battery)

 

 

Completes 10 chair stands (%)

83

94

0.184

        Time to complete (seconds)

32 ± 8

23 ± 5

<0.001

 

 

 

 

Holds semi tandem stand 30 seconds (%)

94

97

0.610

 

 

 

 

Holds tandem stand 30 seconds (%)

83

83

0.149

 

 

 

 

Holds one leg stand 30 seconds (%)

17

100

<0.001

 

 

 

 

Gait Speed (m/s)

0.86

1.06

0.005

 

 

 

 

Body Composition by DEXA

 

 

 

BMI (kg/m2)

28 ± 6

25 ± 4

0.079

 

 

 

 

Bilateral arms

 

 

 

     Total fat mass (g)

3177 ± 1155

2559 ± 989

0.046

     Total lean mass (g)

4262 ± 1070

4337 ± 1315

0.836

 

 

 

 

Bilateral legs

 

 

 

     Total fat mass (g)

10334 ± 4352

8965 ± 3830

0.242

     Total lean mass (g)

13141 ± 2853

13600 ± 3242

0.538

 

 

 

 

Trunk

 

 

 

     Total fat mass (g)

16360 ± 3834

13603 ± 5915

0.079

     Total lean mass (g)

19235 ± 2533

20889 ± 4311

0.140

 

 

 

 

Total Body

 

 

 

     Total fat mass (g)

30915 ± 8614

25942 ± 9772

0.073

     Total lean mass (g)

39995 ± 6065

42216 ± 8898

0.346

 

 

 

 

 


Disclosure:

R. L. Manno,
None;

A. C. Gelber,
None;

P. Seo,
None;

S. M. Levine,

CE Outcomes,

5,

Up to Date,

7;

S. R. Ghazarian,
None;

P. H. Chen,
None;

K. J. Stewart,
None;

J. Metter,
None;

L. Ferrucci,
None;

K. R. Fontaine,
None.

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