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Comparative evaluation of clinical and inflammatory factors in response to the pharmacological managements in metabolic syndrome

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Abstract

Our study focused to assess the effect of various potential treatments on components of metabolic syndrome (MetS). This is a prospective, open-label, parallel group and randomized control trial of 90-day duration in which patients (n = 159) were randomly assigned in four groups to receive “diet and lifestyle modification” (n = 40), “metformin 500 mg twice daily” (n = 39), “pioglitazone 15 mg once daily” (n = 39), and “rosuvastatin 10 mg once daily” (n = 41). Clinical, biochemical, and inflammatory markers of each participant were evaluated. Fasting plasma glucose (FPG) level was lower in all except rosuvastatin group while HDL-cholesterol level increased in rosuvastatin group only (p < 0.05). Serum triglyceride was significantly and comparably decreased in both pioglitazone and rosuvastatin group (p < 0.05). Significant decrease in hsCRP and increase in serum adiponectin (p < 0.05) were reported in all the groups from baseline. The study can add a step forward in devising standard pharmacotherapeutic regimen beyond the current treatment modalities.

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Acknowledgments

Authors are thankful to Mr. VK Saini and Mr. Durgesh Yadav for the technical support. Authors are also thankful to the staff of the department of medicine for the recruitment of patients. The study was not supported by any external funding agency.

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Correspondence to Sanjay Khattri.

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The authors declare that they have no conflict of interest.

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All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.

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Suraj S. Yadav has Equal contribution as first author

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Jain, A., Yadav, S.S., Dwivedi, P. et al. Comparative evaluation of clinical and inflammatory factors in response to the pharmacological managements in metabolic syndrome. Int J Diabetes Dev Ctries 37, 464–469 (2017). https://doi.org/10.1007/s13410-016-0519-0

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  • DOI: https://doi.org/10.1007/s13410-016-0519-0

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