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Increased plasma DPP4 activity predicts new-onset hypertension in Chinese over a 4-year period: possible associations with inflammation and oxidative stress

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Abstract

To investigate whether increased dipeptidyl peptidase 4 (DPP4) activity predicts new-onset hypertension in Chinese patients. A prospective study was conducted for 1884 adults (804 men/1080 women) aged 18–70 years without hypertension. Participants were examined in 2007 (baseline) and 2011 (follow-up) and circulating DPP4 activity, mannose 6-phosphate receptor (M6P-R) concentration, inflammatory markers and oxidative stress parameters were measured. After a 4-year follow-up, 296 individuals developed hypertension with an incidence of 39 per 1000 patient years. In multiple linear regression analyses, baseline DPP4 activity was an independent predictor of an increase in M6P-R, inflammatory markers and oxidative stress parameters over a 4-year period (all P<0.01). Cox proportional hazards models revealed that DPP4 activity independently predicted the risk of developing hypertension (relative risk 2.68 (95% confidence interval 1.71–4.21) P<0.01). Our results indicate that DPP4 activity is an important predictor of hypertension onset in apparently healthy Chinese individuals. This finding may have important implications for understanding the effects of DPP4 in promoting inflammation and oxidative stress in the pathogenesis of hypertension.

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Acknowledgements

We gratefully acknowledge the residents and nurses of the Department of Endocrinology of Yulin Community Hospital, the First People’s Hospital of Longquan and the First People’s Hospital of Liangshan Yi Nationality Autonomy District for their diligent work in collecting demographic data and blood samples. This study was supported by grants from the Chinese Medical Association Foundation and Chinese Diabetes Society (No. 07020470055).

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Correspondence to H Tian.

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Zheng, T., Chen, T., Liu, Y. et al. Increased plasma DPP4 activity predicts new-onset hypertension in Chinese over a 4-year period: possible associations with inflammation and oxidative stress. J Hum Hypertens 29, 424–429 (2015). https://doi.org/10.1038/jhh.2014.111

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