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Is non-biological treatment of rheumatoid arthritis as good as biologics? 被引量:3
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作者 Jyoti Ranjan Parida durga prasanna misra +1 位作者 Anupam Wakhlu Vikas Agarwal 《World Journal of Orthopedics》 2015年第2期278-283,共6页
The management of rheumatoid arthritis(RA) in the past three decades has undergone a paradigm shift from symptomatic relief to a "treat-to-target" approach. This has been possible through use of various conv... The management of rheumatoid arthritis(RA) in the past three decades has undergone a paradigm shift from symptomatic relief to a "treat-to-target" approach. This has been possible through use of various conventional and biologic disease modifying anti-rheumatic drugs(DMARDs) which target disease pathogenesis at a molecular level. Cost and infection risk preclude regular use of biologics in resource-constrained settings. In therecent years, evidence has emerged that combination therapy with conventional DMARDs is not inferior to biologics in the management of RA and is a feasible cost-effective option. 展开更多
关键词 Rheumatoid arthritis Disease modifying drugs BIOLOGICS Methotrexate SULFASALAZINE LEFLUNOMIDE CYCLOSPORINE HYDROXYCHLOROQUINE Tumor necrosis factor Remission RADIOLOGIC outcome
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Bidirectional link between diabetes mellitus and coronavirus disease 2019 leading to cardiovascular disease:A narrative review 被引量:1
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作者 Vijay Viswanathan Anudeep Puvvula +13 位作者 Ankush D Jamthikar Luca Saba Amer M Johri Vasilios Kotsis Narendra N Khanna Surinder K Dhanjil Misha Majhail durga prasanna misra Vikas Agarwal George D Kitas Aditya M Sharma Raghu Kolluri Subbaram Naidu Jasjit S Suri 《World Journal of Diabetes》 SCIE 2021年第3期215-237,共23页
Coronavirus disease 2019(COVID-19)is a global pandemic where several comorbidities have been shown to have a significant effect on mortality.Patients with diabetes mellitus(DM)have a higher mortality rate than non-DM ... Coronavirus disease 2019(COVID-19)is a global pandemic where several comorbidities have been shown to have a significant effect on mortality.Patients with diabetes mellitus(DM)have a higher mortality rate than non-DM patients if they get COVID-19.Recent studies have indicated that patients with a history of diabetes can increase the risk of severe acute respiratory syndrome coronavirus 2 infection.Additionally,patients without any history of diabetes can acquire newonset DM when infected with COVID-19.Thus,there is a need to explore the bidirectional link between these two conditions,confirming the vicious loop between“DM/COVID-19”.This narrative review presents(1)the bidirectional association between the DM and COVID-19,(2)the manifestations of the DM/COVID-19 loop leading to cardiovascular disease,(3)an understanding of primary and secondary factors that influence mortality due to the DM/COVID-19 loop,(4)the role of vitamin-D in DM patients during COVID-19,and finally,(5)the monitoring tools for tracking atherosclerosis burden in DM patients during COVID-19 and“COVID-triggered DM”patients.We conclude that the bidirectional nature of DM/COVID-19 causes acceleration towards cardiovascular events.Due to this alarming condition,early monitoring of atherosclerotic burden is required in“Diabetes patients during COVID-19”or“new-onset Diabetes triggered by COVID-19 in Non-Diabetes patients”. 展开更多
关键词 COVID-19 Diabetes mellitus Bidirectional association Cardiovascular disease Atherosclerotic burden Imaging tools
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Scleroderma: Not an orphan disease any more
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作者 durga prasanna misra Abhra Chandra Chowdhury +1 位作者 Sanat Phatak Vikas Agarwal 《World Journal of Rheumatology》 2015年第3期131-141,共11页
Scleroderma(or systemic sclerosis) is a rare disease associated with significant morbidity and mortality.Although previously thought to have a uniformly poor prognosis,the outlook has changed in recent years.We review... Scleroderma(or systemic sclerosis) is a rare disease associated with significant morbidity and mortality.Although previously thought to have a uniformly poor prognosis,the outlook has changed in recent years.We review recent insights into the pathogenesis,clinical features,assessment and management of scleroderma. 展开更多
关键词 PULMONARY HYPERTENSION SCLERODERMA INTERSTITIAL lung disease Raynauds phenomenon FIBROSIS
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Study of hsCRP, adiponectin, NF-κB in low bodyweight, standard bodyweight and obese subjects with type 2 diabetes mellitus in India
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作者 Sidhartha Das durga prasanna misra Pratima Kumari Sahu 《Journal of Diabetes Mellitus》 2012年第4期386-392,共7页
Introduction: Low bodyweight type 2 DM is a distinct clinical entity having many inherent peculiarities seen in India and developing countries, constituting 11% to 25% of type 2 diabetic subjects. Our study aimed at a... Introduction: Low bodyweight type 2 DM is a distinct clinical entity having many inherent peculiarities seen in India and developing countries, constituting 11% to 25% of type 2 diabetic subjects. Our study aimed at assessing the prevalence of inflammatory markers like hsCRP, adiponectin and NF-κB expression in peripheral blood mononuclear cells in subjects with type 2 DM in relation to BMI. Materials and Methods: 57 consecutive type 2 diabetics were recruited for study, classified as Low Bodyweight (A = BMI < 18.5), Standard weight (B = BMI 18.5 - 24.99) and Obese (C = BMI ≥ 25). Group D comprised 14 healthy controls. They were evaluated for clinical parameters, FBG, 2hrPPBG, HbA1c, lipid profile and above mentioned inflammatory markers. Results: Serum hsCRP was significantly higher in all group of diabetics as compared to Group D but was lowest in Group A. Adiponectin levels were highest in Group D, similar in Groups B and C but lowest in Group A. NF-κB expression, though higher in diabetic subjects than controls (OD = 0.041 ± 0.006), was least in Group A (OD = 0.045 ± 0.005). Discussion and Conclusion: Our study revealed that Indians with type 2DM are in a pro-inflamematory state. Low bodyweight type 2 diabetics had the least pro-inflammatory load. This further supported the earlier observation of lesser macrovascular disease load and testifying that Low Bodyweight type2DM constitutes a distinct entity. 展开更多
关键词 LOW BODYWEIGHT Type 2 DM HSCRP NF-ΚB ADIPONECTIN
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