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  Citation statistics : Table of Contents
   2017| December  | Volume 12 | Issue 4  
    Online since November 16, 2017

 
 
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ORIGINAL ARTICLES
Assessment of extent of skin involvement in scleroderma using shear wave elastography
Anupam Wakhlu, Abhra Chandra Chowdhury, Namita Mohindra, Saumya Ranjan Tripathy, Durga Prasanna Misra, Vikas Agarwal
December 2017, 12(4):194-198
DOI:10.4103/injr.injr_41_17  
Introduction: Scleroderma (systemic sclerosis [SSc]) is a rare autoimmune disease which manifests as fibrosis in the skin and other internal organs. Conventionally, the modified Rodnan skin score (MRSS) has been used to quantify the extent of skin fibrosis (resulting in skin tightness) in SSc. This technique, although widely validated, is limited by the requirement of a trained, experienced assessor. Recent literature suggests that utilization of the objective ultrasound-based assessment of skin fibrosis utilizing shear wave elastography (SWE) may be a more robust technique to detect early skin tightness in SSc. Methods: We evaluated the use of SWE (assessed by an experienced radiologist) in 24 patients with SSc compared with 16 healthy controls. Results: Our patients were predominantly females, with median disease duration of 1.5 years and median MRSS of 17. There was minimal intraobserver variation in the assessment of SWE. Patients with SSc had higher SWE values (mean elasticity [Emean]) compared to healthy controls at most assessed sites for the MRSS. The Emeancorrelated significantly at all sites with the MRSS scores. At the sites where MRSS was scored as 0 (normal), the Emeanin patients with SSc was higher when compared with similarly clinical normal skin in patients with SSc, suggesting potential early involvement of these areas of the skin with fibrosis. Conclusion: SWE is a promising tool to objectively assess skin fibrosis in SSc and may be useful in detecting early, subclinical skin involvement in this disease.
  2 1,204 140
Evaluation of peripheral enthesitis in spondyloarthritis: Ultrasonography versus clinical examination
Anupam Wakhlu, Saumya Ranjan Tripathy, Archana Wakhlu, Durgesh Srivastava, Rasmi Ranjan Sahoo
December 2017, 12(4):199-203
DOI:10.4103/injr.injr_39_17  
Background: Enthesitis is an important feature of spondyloarthritis but may often be subclinical. Data is sparse, especially from India, on the ultrasonography (USG) detection of enthesitis in these patients. The present study aimed to find the prevalence and pattern of entheseal involvement assessed clinically and by USG. Methods: Fifty-two spondyloarthritis, 26 rheumatoid arthritis, and 26 healthy controls were evaluated for enthesitis by clinical examination and by USG using 2014 OMERACT consensus group definitions at bilateral Achilles insertion on the calcaneus, plantar fascia attachment on the calcaneus, quadriceps tendon insertion on the patella, patellar tendon origin from the inferior pole of the patella, and patellar tendon insertion on the tibial tuberosity. At least one ultrasonographic finding at any of the above sites was considered positive for enthesitis. Results: The number of entheseal sites screened in spondyloarthritis patients was 520 and 260 each in rheumatoid arthritis and healthy controls. USG (sensitivity - 94.2%) was better in detecting enthesitis than clinical examination (sensitivity - 69.2%). Clinical examination was highly specific (100%) compared to USG (55.7%) in differentiating from rheumatoid arthritis and healthy controls. USG alone without clinical findings was positive at 23.8% of sites while clinical examination alone without USG findings was positive at 5.2% of sites. Frequency of enthesitis in rheumatoid arthritis was not more than healthy controls (6.1% vs. 8.1%, respectively) and was much less than spondyloarthritis (34%). Conclusion: USG is a good screening tool for detection of enthesitis but cannot replace clinical examination completely.
  2 1,313 172
LETTER TO EDITOR
Ibuprofen: When the savior turns tormentor!
R Kirthi, Joy Varghese, Mayank Jain, Mukul Vij, Jayanthi Venkataraman
December 2017, 12(4):230-231
DOI:10.4103/injr.injr_96_17  
  1 910 158
REVIEW ARTICLE
Vitamin D and autoimmune diseases
Shir Azrielant, Yehuda Shoenfeld
December 2017, 12(4):219-222
DOI:10.4103/injr.injr_99_17  
Vitamin D and its deficiency are becoming a subject of great interest in recent years. In addition to the well-known role of vitamin D in maintaining bone health, evidence from recent years are accumulating in favor of its importance in the functioning of the immune system. The association between vitamin D deficiency and autoimmune diseases has been supported by epidemiological studies, demonstrating higher prevalence of vitamin D deficiency among autoimmune patients, in comparison to the general population. Vitamin D was also associated to various autoimmune diseases in both molecular and interventional studies; among the associated diseases are: systemic lupus erythematosus, type 1 diabetes mellitus, multiple sclerosis and others. In this review, relevant literature on the association between autoimmunity and vitamin D deficiency will be reviewed and discussed, as well as a summary of important recommendations for vitamin D supplementations in autoimmune patients.
  1 5,008 457
BOOK REVIEW
Ankylosing spondylitis-axial spondyloarthritis
Aanand Narayan Malaviya
December 2017, 12(4):232-232
DOI:10.4103/0973-3698.215927  
  - 819 133
EDITORIALS
Plagiarism: Software-based detection and the importance of (Human) hardware
Durga Prasanna Misra, Vinod Ravindran, Vikas Agarwal
December 2017, 12(4):188-189
DOI:10.4103/0973-3698.218553  
  - 788 111
Ultrasonography in the evaluation of peripheral enthesitis in spondyloarthropathy
Sumeet Agrawal, Ashok Kumar
December 2017, 12(4):190-191
DOI:10.4103/0973-3698.218554  
  - 566 85
Quantitating skin thickness in systemic sclerosis: The way ahead
Shefali Sharma, Aadhaar Dhooria
December 2017, 12(4):192-193
DOI:10.4103/0973-3698.218555  
  - 826 108
FROM THE EDITORS DESK
From the Editor's desk
Vinod Ravindran
December 2017, 12(4):187-187
DOI:10.4103/0973-3698.218556  
  - 554 77
IMAGES IN RHEUMATOLOGY
Multicentric reticulohistiocytosis: Unusual presentation of an uncommon disease
Jeet Hemant Kumar Patel, Neeraj Jain, Lalit Duggal, Shilpa Garg, Bhandari Gurbir, Seema Rao, Amal Basnet
December 2017, 12(4):223-225
DOI:10.4103/injr.injr_66_17  
  - 1,034 115
Bilateral L4 pedicle stress fracture: An unusual cause of low back pain in an adolescent
V Sivakumar, Venkatraman Indiran
December 2017, 12(4):226-227
DOI:10.4103/injr.injr_85_17  
  - 2,232 124
Cutaneous T-cell lymphoma presenting as panniculitis with arthritis
Rasmi Ranjan Sahoo, Anupam Wakhlu, Kiranpreet Malhotra, Puneet Kumar
December 2017, 12(4):228-229
DOI:10.4103/injr.injr_59_17  
  - 867 82
ORIGINAL ARTICLES
Helicobacter Pylori infection in systemic sclerosis and its association with upper gastrointestinal dysfunction
Chilukuri Balaji, Mahendran Bhuvanesh, Chinnadurai Saranya, Ramamoorthy Ramesh, Mayilsamy Saravanan, Sankaralingam Rajeswari
December 2017, 12(4):204-208
DOI:10.4103/injr.injr_62_17  
Background: Immune dysregulation triggered by environmental events (including microbes) have been implicated in the etiopathogenesis of systemic sclerosis (SSc). Helicobacter pylori (H. pylori) a pathogen well known to cause gastric ulcers and has been associated with several autoimmune diseases. However, the role of H. pylori in SSc has not been widely reported. The objective of the study was to estimate the prevalence of H. pylori infection in SSc patients and analyze its clinical associations. Methods: This study comprised 55 patients who satisfied ACR/EULAR 2013 classification criteria for SSc and 25 age and sex-matched healthy controls. Demographic, clinical, laboratory, and immunological parameters were recorded. Upper gastrointestinal (GI) endoscopy was done. Anti-H. pylori IgG levels (RU/ml) were estimated by ELISA and results analyzed by SPSS. Results: Baseline characteristics were comparable in both groups. Prevalence of H. pylori infection was high in SSc patients in comparison to controls (61.8% vs. 24%). Anti-H. pylori IgG levels were high in SSc patients in comparison to controls (mean 65 RU/ml vs. 25.3RU/ml; P = 0.003). SSc patients with symptomatic GI involvement had higher anti-H. pylori IgG levels than asymptomatic patients (mean 118.3 RU/ml vs. 20.7 RU/ml; P < 0.001). Anti-H. pylori IgG levels were not significantly different between diffuse cutaneous SSc and limited cutaneous SSc (mean 72.9 RU/ml vs. 54.1RU/ml; P = 0.289). Anti-H. pylori IgG antibody levels showed no correlation with disease duration, erythrocyte sedimentation rate, C-reactive protein, interstitial lung disease, and modified Rodnan Skin Score. Conclusion: SSc patients have high seropositivity for anti-H. pylori IgG antibodies. High anti-H. pylori IgG antibody titers are associated with symptomatic upper GI dysfunction.
  - 1,063 111
A comparison of 3 rheumatoid arthritis disease activity indices in routine clinical practice
Amit Kumar Das, Rathindra Nath Sarkar, Chandan Kumar Das, Ritasman Baisya, Urmimala Bhattacharjee, Pallab Biswas, Akashdip Bhattacharya
December 2017, 12(4):209-213
DOI:10.4103/injr.injr_87_17  
Objective: The objective of this study was to appraise the correlation and agreement of RAPID 3 with DAS 28 and CDAI in terms of measuring disease activity/severity and for monitoring response to treatment at 2 and 4 month follow up. Methods: 105 adult literate persons having rheumatoid arthritis according to the 2010 ACR EULAR revised criteria were included. They were evaluated for disease activity by DAS 28, CDAI, and RAPID 3 scores. Response to treatment at 2 month and 4 month follow up was measured by these scores. Achievement of treatment target was defined as conversion from high/moderate disease activity at initial visit to low activity/remission at follow up visit. Result: The mean DAS 28 (0-10), CDAI (0-76) , RAPID 3 (0-30) were 4.73 , 16.72, 10.72 respectively. There was substantial agreement between DAS 28 and RAPID 3 severity categories (kappa = 0.959, P < 0.0001) and also between CDAI and RAPID 3. Conclusion: In a busy clinical setting, our study has shown usefulness of RAPID3 compared to the two most commonly used indices to assess disease activity in RA, both in terms of measuring quantitative disease activity as well as monitoring of treatment response at follow up visits.
  - 1,153 127
The protein tyrosine phosphatase, nonreceptor type 22-1858C->T (rs2476601) polymorphism is not a genetic risk factor for systemic lupus erythematosus in Indian Tamils
Panneer Devaraju, Reena Gulati, Durga Prasanna Misra, Vir Singh Negi
December 2017, 12(4):214-218
DOI:10.4103/injr.injr_90_17  
Background: Systemic lupus erythematosus (SLE), a systemic autoimmune disease, occurs due to disruption of immune homeostasis against self-antigens. The etiology of SLE is complex and multiple genetic factors contribute to disease susceptibility and clinical phenotypes. Protein tyrosine phosphatase, nonreceptor type 22 (PTPN22) is a lymphoid-specific phosphatase that negatively regulates T-cell receptor signaling and is responsible for the maintenance of T-cell homeostasis. Genetic aberrations affecting the function of PTPN22 result in the proliferation of autoreactive T-cells and development of autoimmune diseases. Methods: We carried out a case–control genetic study to analyze the association of PTPN22 R620W polymorphism (rs2476601) with disease susceptibility and clinical and autoantibody profile in Indian Tamils with SLE. Three hundred SLE patients satisfying the 1997 revised American College of Rheumatology classification criteria for SLE were enrolled in the study. Disease activity was measured using the SLE Disease Activity Index. We recruited 460 age-, sex-, and ethnicity-matched individuals without a family history of autoimmune diseases as control population. Genomic DNA was extracted from the blood sample by salting-out method. The PTPN22-1858C->T (rs2476601) polymorphism was screened by polymerase chain reaction-restriction fragment length polymorphism. Results: The frequency of the ancestral allele “C” was similar in both cases and controls (99.3% and 99.8%, respectively) and the mutant allele “T” was less frequent in South Indian Tamil population; it did not influence clinical or serological phenotypes. Conclusion: Our findings suggest that the PTPN22 (rs2476601) polymorphism is less frequent and did not confer a risk for lupus or its associated clinical or serological phenotypes in South Indian Tamils.
  - 680 64