. | IBM (n = 50) . | IIM (n = 65) . | Controls (n = 294) . | . |
---|---|---|---|---|
Neurological | ||||
Dementia | 3 (6) | 7 (10.8) | 31 (10.5) | |
Parkinson’s disease | 2 (4) | 2 (3.1) | 17 (5.8) | |
Peripheral neuropathy** | 18 (36) | 15 (23.1) | 51 (17.4)** | |
Conditions that may cause a peripheral neuropathy: | ||||
| 16(32) | 19(29) | 129(44) | |
| 11(22) | 31(48)** | 87(30) | |
| 3(6) | 3(5) | 8(3) | |
| 4(8) | 1(2) | 8(3)# | |
Rheumatological | ||||
Lupus erythematous*** | 0 | 6(9)* | 1(<1) | |
Systemic scleroderma*** | 1(2) | 7(11) | 0 | |
Sjögren syndrome* | 3(6) | 2(3) | 3(1)* | |
RA* | 4(8) | 8(12) | 13(5) | |
Any of the above*** | 8(16) | 19(29) | 15(5)** | |
Malignancies | ||||
Malignancy of any type | 20 (40) | 23 (35.4) | 92 (31.3) | |
Solid cancers | 16 (32) | 21 (32.3) | 88 (29.9) | |
Haematologic malignancies* | 5 (10) | 3 (4.6) | 8 (2.7)* | |
| Diffuse large B cell (1) Marginal zone (1) | Hodgkin’s (1) Waldenstrom (1) Diffuse large B cell (1) | Difffuse large B cell (4) Marginal zone (1) | |
| TLGL(2) | 0 | CLL(1) | |
| Multiple myeloma (1) | 0 | 0 | |
| 0 | 0 | 2 | |
Infectious | ||||
Hepatitis B | 0 0 | 0 0 | 2 (0.7) | |
Hepatitis C | 0 0 | 1 (1.5) | 2 (0.7) | |
HIV | 0 0 | 00 | 00 |
. | IBM (n = 50) . | IIM (n = 65) . | Controls (n = 294) . | . |
---|---|---|---|---|
Neurological | ||||
Dementia | 3 (6) | 7 (10.8) | 31 (10.5) | |
Parkinson’s disease | 2 (4) | 2 (3.1) | 17 (5.8) | |
Peripheral neuropathy** | 18 (36) | 15 (23.1) | 51 (17.4)** | |
Conditions that may cause a peripheral neuropathy: | ||||
| 16(32) | 19(29) | 129(44) | |
| 11(22) | 31(48)** | 87(30) | |
| 3(6) | 3(5) | 8(3) | |
| 4(8) | 1(2) | 8(3)# | |
Rheumatological | ||||
Lupus erythematous*** | 0 | 6(9)* | 1(<1) | |
Systemic scleroderma*** | 1(2) | 7(11) | 0 | |
Sjögren syndrome* | 3(6) | 2(3) | 3(1)* | |
RA* | 4(8) | 8(12) | 13(5) | |
Any of the above*** | 8(16) | 19(29) | 15(5)** | |
Malignancies | ||||
Malignancy of any type | 20 (40) | 23 (35.4) | 92 (31.3) | |
Solid cancers | 16 (32) | 21 (32.3) | 88 (29.9) | |
Haematologic malignancies* | 5 (10) | 3 (4.6) | 8 (2.7)* | |
| Diffuse large B cell (1) Marginal zone (1) | Hodgkin’s (1) Waldenstrom (1) Diffuse large B cell (1) | Difffuse large B cell (4) Marginal zone (1) | |
| TLGL(2) | 0 | CLL(1) | |
| Multiple myeloma (1) | 0 | 0 | |
| 0 | 0 | 2 | |
Infectious | ||||
Hepatitis B | 0 0 | 0 0 | 2 (0.7) | |
Hepatitis C | 0 0 | 1 (1.5) | 2 (0.7) | |
HIV | 0 0 | 00 | 00 |
P = comparison of the three groups; NS: not significant with P >0.05, P1 = IBM vs IIM, P2 = IBM vs Categorical variables are displayed as n (percentage). The P-value corresponding to comparison of the three groups is shown in the first column, P-value for IBM vs IIM group is shown in ‘IIM’ column, and P-value for IBM vs population controls is shown in ‘population controls’ column.
0.01≤P-value < 0.05;
P-value <0.01;
P-value <0.001;
P-value <0.0001;
P-value = 0.06.
IBM: inclusion body myositis; IIM: inflammatory myopathy.
. | IBM (n = 50) . | IIM (n = 65) . | Controls (n = 294) . | . |
---|---|---|---|---|
Neurological | ||||
Dementia | 3 (6) | 7 (10.8) | 31 (10.5) | |
Parkinson’s disease | 2 (4) | 2 (3.1) | 17 (5.8) | |
Peripheral neuropathy** | 18 (36) | 15 (23.1) | 51 (17.4)** | |
Conditions that may cause a peripheral neuropathy: | ||||
| 16(32) | 19(29) | 129(44) | |
| 11(22) | 31(48)** | 87(30) | |
| 3(6) | 3(5) | 8(3) | |
| 4(8) | 1(2) | 8(3)# | |
Rheumatological | ||||
Lupus erythematous*** | 0 | 6(9)* | 1(<1) | |
Systemic scleroderma*** | 1(2) | 7(11) | 0 | |
Sjögren syndrome* | 3(6) | 2(3) | 3(1)* | |
RA* | 4(8) | 8(12) | 13(5) | |
Any of the above*** | 8(16) | 19(29) | 15(5)** | |
Malignancies | ||||
Malignancy of any type | 20 (40) | 23 (35.4) | 92 (31.3) | |
Solid cancers | 16 (32) | 21 (32.3) | 88 (29.9) | |
Haematologic malignancies* | 5 (10) | 3 (4.6) | 8 (2.7)* | |
| Diffuse large B cell (1) Marginal zone (1) | Hodgkin’s (1) Waldenstrom (1) Diffuse large B cell (1) | Difffuse large B cell (4) Marginal zone (1) | |
| TLGL(2) | 0 | CLL(1) | |
| Multiple myeloma (1) | 0 | 0 | |
| 0 | 0 | 2 | |
Infectious | ||||
Hepatitis B | 0 0 | 0 0 | 2 (0.7) | |
Hepatitis C | 0 0 | 1 (1.5) | 2 (0.7) | |
HIV | 0 0 | 00 | 00 |
. | IBM (n = 50) . | IIM (n = 65) . | Controls (n = 294) . | . |
---|---|---|---|---|
Neurological | ||||
Dementia | 3 (6) | 7 (10.8) | 31 (10.5) | |
Parkinson’s disease | 2 (4) | 2 (3.1) | 17 (5.8) | |
Peripheral neuropathy** | 18 (36) | 15 (23.1) | 51 (17.4)** | |
Conditions that may cause a peripheral neuropathy: | ||||
| 16(32) | 19(29) | 129(44) | |
| 11(22) | 31(48)** | 87(30) | |
| 3(6) | 3(5) | 8(3) | |
| 4(8) | 1(2) | 8(3)# | |
Rheumatological | ||||
Lupus erythematous*** | 0 | 6(9)* | 1(<1) | |
Systemic scleroderma*** | 1(2) | 7(11) | 0 | |
Sjögren syndrome* | 3(6) | 2(3) | 3(1)* | |
RA* | 4(8) | 8(12) | 13(5) | |
Any of the above*** | 8(16) | 19(29) | 15(5)** | |
Malignancies | ||||
Malignancy of any type | 20 (40) | 23 (35.4) | 92 (31.3) | |
Solid cancers | 16 (32) | 21 (32.3) | 88 (29.9) | |
Haematologic malignancies* | 5 (10) | 3 (4.6) | 8 (2.7)* | |
| Diffuse large B cell (1) Marginal zone (1) | Hodgkin’s (1) Waldenstrom (1) Diffuse large B cell (1) | Difffuse large B cell (4) Marginal zone (1) | |
| TLGL(2) | 0 | CLL(1) | |
| Multiple myeloma (1) | 0 | 0 | |
| 0 | 0 | 2 | |
Infectious | ||||
Hepatitis B | 0 0 | 0 0 | 2 (0.7) | |
Hepatitis C | 0 0 | 1 (1.5) | 2 (0.7) | |
HIV | 0 0 | 00 | 00 |
P = comparison of the three groups; NS: not significant with P >0.05, P1 = IBM vs IIM, P2 = IBM vs Categorical variables are displayed as n (percentage). The P-value corresponding to comparison of the three groups is shown in the first column, P-value for IBM vs IIM group is shown in ‘IIM’ column, and P-value for IBM vs population controls is shown in ‘population controls’ column.
0.01≤P-value < 0.05;
P-value <0.01;
P-value <0.001;
P-value <0.0001;
P-value = 0.06.
IBM: inclusion body myositis; IIM: inflammatory myopathy.
This PDF is available to Subscribers Only
View Article Abstract & Purchase OptionsFor full access to this pdf, sign in to an existing account, or purchase an annual subscription.