Table 2.

Relative risk of CLL in relation to personal and family history of autoimmune conditions



Personal history

Family history
Autoimmune condition
pa
co
OR
95% CI
pa
co
OR
95% CI
Autoantibodies detectable         
Systemic involvement          
Polymyositis/dermatomyositis   17   22   1.58   0.84-2.99   15   36   0.87   0.47-1.59  
Rheumatoid arthritis   68   136   1.03   0.76-1.38   49   129   0.81   0.58-1.13  
Sjögren syndrome   6   3   3.96   0.99-15.85   1   3   0.71   0.07-6.81  
Systemic lupus erythematosus   3   8   0.83   0.22-3.16   13   23   1.22   0.62-2.42  
Systemic sclerosis   7   5   2.75   0.87-8.69   5   6   1.89   0.58-6.23  
Organ involvement          
Addison disease   0   8   0   (P = .062)   4   4   2.25   0.56-9.03  
Amyotrophic lateral sclerosis   2   7   0.54   0.11-2.61   3   0   Inf*  (P = .032)  
Autoimmune hemolytic anemia   54   1   108.4*  14.9-784   1   5   0.42   0.05-3.58  
Chronic rheumatic heart disease   18   67   0.55*  0.33-0.93   14   23   1.44   0.74-2.81  
Discoid lupus erythematosus   0   1   0   (P = 1.00)   0   2   0   (P = 1.00)  
Grave disease   3   13   0.50   0.14-1.77   8   19   0.90   0.39-2.06  
Hashimoto thyroiditis   2   4   1.07   0.20-5.88   4   2   4.75   0.87-25.99  
Immune thrombocytopenic purpura   5   5   2.16   0.62-7.51   0   8   0   (P = .062)  
Insulin-dependent diabetes   0   0   NA   NA   12   17   1.80   0.86-3.78  
Localized scleroderma   0   0   NA   NA   1   0   Inf   (P = .32)  
Lupoid hepatitis   0   0   NA   NA   0   0   NA   NA  
Multiple sclerosis   9   25   0.80   0.37-1.72   20   37   1.18   0.68-2.04  
Myasthenia gravis   2   1   4.78   0.43-53.02   4   3   2.71   0.61-12.13  
Pernicious anemia   31   32   1.94*  1.18-3.18   9   18   1.21   0.54-2.70  
Polyarteritis nodosa   1   1   1.93   0.12-30.91   0   3   0   (P = .56)  
Primary biliary cirrhosis   1   5   0.42   0.05-3.62   2   3   1.38   0.23-8.31  
Wegener granulomatosis   0   2   0   (P = 1.00)   0   3   0   (P = .56)  
Autoantibodies not detectable         
Ankylosing spondylitis   6   9   1.41   0.50-3.98   11   13   1.71   0.76-3.82  
Behcet disease   0   0   NA   NA   0   0   NA   NA  
Chorea minor   0   0   NA   NA   0   0   NA   NA  
Crohn disease   4   21   0.42   0.14-1.21   28   55   1.13   0.73-1.74  
Polymyalgia rheumatica   22   42   1.06   0.63-1.79   11   24   1.08   0.53-2.21  
Psoriasis   10   35   0.57   0.28-1.15   15   32   1.03   0.56-1.91  
Reiter disease   0   2   0   (P = 1.00)   8   11   1.66   0.67-4.14  
Rheumatic fever   3   9   0.66   0.18-2.43   7   18   0.84   0.35-2.02  
Sarcoidosis   8   19   0.90   0.39-2.07   12   31   0.82   0.42-1.61  
Ulcerative colitis
 
9
 
22
 
0.89
 
0.41-1.94
 
39
 
59
 
1.40
 
0.94-2.08
 


Personal history

Family history
Autoimmune condition
pa
co
OR
95% CI
pa
co
OR
95% CI
Autoantibodies detectable         
Systemic involvement          
Polymyositis/dermatomyositis   17   22   1.58   0.84-2.99   15   36   0.87   0.47-1.59  
Rheumatoid arthritis   68   136   1.03   0.76-1.38   49   129   0.81   0.58-1.13  
Sjögren syndrome   6   3   3.96   0.99-15.85   1   3   0.71   0.07-6.81  
Systemic lupus erythematosus   3   8   0.83   0.22-3.16   13   23   1.22   0.62-2.42  
Systemic sclerosis   7   5   2.75   0.87-8.69   5   6   1.89   0.58-6.23  
Organ involvement          
Addison disease   0   8   0   (P = .062)   4   4   2.25   0.56-9.03  
Amyotrophic lateral sclerosis   2   7   0.54   0.11-2.61   3   0   Inf*  (P = .032)  
Autoimmune hemolytic anemia   54   1   108.4*  14.9-784   1   5   0.42   0.05-3.58  
Chronic rheumatic heart disease   18   67   0.55*  0.33-0.93   14   23   1.44   0.74-2.81  
Discoid lupus erythematosus   0   1   0   (P = 1.00)   0   2   0   (P = 1.00)  
Grave disease   3   13   0.50   0.14-1.77   8   19   0.90   0.39-2.06  
Hashimoto thyroiditis   2   4   1.07   0.20-5.88   4   2   4.75   0.87-25.99  
Immune thrombocytopenic purpura   5   5   2.16   0.62-7.51   0   8   0   (P = .062)  
Insulin-dependent diabetes   0   0   NA   NA   12   17   1.80   0.86-3.78  
Localized scleroderma   0   0   NA   NA   1   0   Inf   (P = .32)  
Lupoid hepatitis   0   0   NA   NA   0   0   NA   NA  
Multiple sclerosis   9   25   0.80   0.37-1.72   20   37   1.18   0.68-2.04  
Myasthenia gravis   2   1   4.78   0.43-53.02   4   3   2.71   0.61-12.13  
Pernicious anemia   31   32   1.94*  1.18-3.18   9   18   1.21   0.54-2.70  
Polyarteritis nodosa   1   1   1.93   0.12-30.91   0   3   0   (P = .56)  
Primary biliary cirrhosis   1   5   0.42   0.05-3.62   2   3   1.38   0.23-8.31  
Wegener granulomatosis   0   2   0   (P = 1.00)   0   3   0   (P = .56)  
Autoantibodies not detectable         
Ankylosing spondylitis   6   9   1.41   0.50-3.98   11   13   1.71   0.76-3.82  
Behcet disease   0   0   NA   NA   0   0   NA   NA  
Chorea minor   0   0   NA   NA   0   0   NA   NA  
Crohn disease   4   21   0.42   0.14-1.21   28   55   1.13   0.73-1.74  
Polymyalgia rheumatica   22   42   1.06   0.63-1.79   11   24   1.08   0.53-2.21  
Psoriasis   10   35   0.57   0.28-1.15   15   32   1.03   0.56-1.91  
Reiter disease   0   2   0   (P = 1.00)   8   11   1.66   0.67-4.14  
Rheumatic fever   3   9   0.66   0.18-2.43   7   18   0.84   0.35-2.02  
Sarcoidosis   8   19   0.90   0.39-2.07   12   31   0.82   0.42-1.61  
Ulcerative colitis
 
9
 
22
 
0.89
 
0.41-1.94
 
39
 
59
 
1.40
 
0.94-2.08
 

P values (2-sided) based on the Fisher exact test are given when patients or control subjects have 0 individuals with the specified condition. ORs for personal history were adjusted for age, calendar time of CLL diagnosis, sex, and region. ORs for family history were adjusted for age, calendar time of CLL diagnosis, sex, region, and personal history of the same disorder.

pa indicates patients; co, control subjects; OR, odd ratio; CI, confidence interval; NA, not applicable; and Inf, infinity.

*

P values <.05.

Close Modal

or Create an Account

Close Modal
Close Modal