Srijana Davuluri

All Publications

• Moving forward together: collaborative landscapes of research in idiopathic inflammatory myopathies and calcinosis. Rheumatology (Oxford, England) Saketkoo, L. A., Valenzuela, A., Kim, S., McCann, L. J., Lood, C., Wahezi, D. M., Werth, V. P., Yi, B., Alexanderson, H., Maillard, S., Pilkington, C., Fligelstone, K., Limbach, B., Orandi, A. B., Regardt, M., Russell, A. M., Davuluri, S., deGroot, I., Ernste, F., Paik, J. J., von Muhlen, C. A., Dimachkie, M. M., Machado, P. M., Naddaf, E., Zulian, F., Chung, L. 2023

  View details for DOI 10.1093/rheumatology/kead331

  View details for PubMedID 37449887

• Extreme Phenotype Approach Identifies Rare Variants in Systemic Sclerosis and Dermatomyositis Patients with Severe Calcinosis Davuluri, S., Kaundal, U., Lood, C., Kapoor, P., Kawano, Y., Dell'Orso, S., Deng, Z., McMahan, Z., Shah, A., Hummers, L., Kastner, D., Wigley, F., Fiorentino, D., Gourh, P., Chung, L. WILEY. 2022: 3297-3300

  View details for Web of Science ID 000877386504154

• Calcinosis in systemic sclerosis. Current opinion in rheumatology Davuluri, S., Lood, C., Chung, L. 2022

  Abstract

  PURPOSE OF REVIEW: The aim of this study was to provide updated information on the prevalence, pathogenesis, diagnostics and therapeutics of calcinosis cutis associated with systemic sclerosis (SSc).RECENT FINDINGS: Observational studies show ethnic and geographical differences in the prevalence of calcinosis. In addition to clinical and serological associations, biochemical studies and in-vivo models have attempted to explain theories behind its pathogenesis, including prolonged state of inflammation, mechanical stress, hypoxia and dysregulation in bone and phosphate metabolism. Long-term use of proton pump inhibitors may increase the risk for calcinosis in SSc. Few single-centre observational studies have shown mild benefit with minocycline and topical sodium thiosulfate.SUMMARY: Calcinosis cutis is the deposition of insoluble calcium in the skin and subcutaneous tissues. It affects up to 40% of SSc patients and causes significant morbidity. Long disease duration, features of vascular dysfunction and osteoporosis have been associated with calcinosis. Altered levels of inorganic pyrophosphate and fibroblast growth factor-23 have been implicated in dysregulated phosphate metabolism that may lead to calcinosis in SSc. Plain radiography can help with diagnosis and quantifying the calcinosis burden. Surgical treatment remains the most effective therapy when feasible. At present, no medical therapies have proven efficacy in large randomized controlled trials.

  View details for DOI 10.1097/BOR.0000000000000896

  View details for PubMedID 35993867

• Calcinosis in dermatomyositis: Origins and possible therapeutic avenues. Best practice & research. Clinical rheumatology Davuluri, S., Duvvuri, B., Lood, C., Faghihi-Kashani, S., Chung, L. 2022: 101768

  Abstract

  Calcinosis, insoluble calcium compounds deposited in skin and other tissues, is a crippling sequela of dermatomyositis. Prolonged disease associated with ongoing inflammation, ischemia, repetitive trauma, and certain autoantibodies are associated with calcinosis. Herein, we describe potential pathogenic mechanisms including the role of mitochondrial calcification. There are no widely effective treatments for calcinosis. We review available pharmacologic therapies for calcinosis including those targeting calcium and phosphorus metabolism; immunosuppressive/anti-inflammatory therapies; and vasodilators. Mounting evidence supports the use of various formulations of sodium thiosulfate in the treatment of calcinosis. Although the early institution of aggressive immunosuppression may prevent calcinosis in juvenile dermatomyositis, only limited data support improvement once it has developed. Minocycline can be useful particularly for lesions associated with surrounding inflammation. Powerful vasodilators, such as prostacyclin analogs, may have promise in the treatment of calcinosis, but further studies are necessary. Surgical removal of lesions when amenable is our treatment of choice.

  View details for DOI 10.1016/j.berh.2022.101768

  View details for PubMedID 35803868