Cardiorespiratory fitness, genetic susceptibility, inflammation and risk of incident type 2 diabetes: A population-based longitudinal study

被引:9
|
作者
Xu, Chenjie [1 ]
Hou, Yabing [2 ]
Si, Keyi [3 ]
Cao, Zhi [4 ]
机构
[1] Hangzhou Normal Univ, Sch Publ Hlth, Hangzhou, Peoples R China
[2] Tianjin Med Univ, Sch Publ Hlth, Tianjin, Peoples R China
[3] Naval Med Univ, Dept Hlth Stat, Shanghai, Peoples R China
[4] Zhejiang Univ, Sch Publ Hlth, Sch Med, Yuhangtang Rd 866, Hangzhou 310058, Peoples R China
来源
关键词
Cardiorespiratory fitness; Genetic susceptibility; Inflammation; Type; 2; diabetes; PHYSICAL-ACTIVITY; ASSOCIATION; EXERCISE; MORTALITY; STRENGTH;
D O I
10.1016/j.metabol.2022.155215
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To examine whether the association between cardiorespiratory fitness (CRF) and type 2 diabetes (T2D) is modified by genetic susceptibility and inflammation. Participants: The prospective study included 57,185 participants (40-70 years) who were free from T2D and received the CRF assessment at enrollment (2006-2010) in the UK biobank. CRF was examined through a submaximal cycle ergometer test and expressed in metabolic equivalent of tasks (METs), genetic susceptibility was quantified using a genetic risk score, and inflammation was assessed according to the concentration of C reactive protein. All these three factors were categorized into tertiles. Results: During a median follow-up of 10.4 years, 5477 (7.0%) cases of T2D were ascertained. CRF was inversely associated with the risk of T2D in a dose-response manner. The hazard ratio (HR) was 0.85 (95% confidence interval [CI]: 0.79-0.92) per 1 MET increment of CRF. There was a significant interaction between CRF and genetic susceptibility to T2D in relation to the risk of T2D (P for interaction = 0.03). Compared with participants with high CRF and low genetic susceptibility, the HR was 4.98 (95% CI: 3.17-7.82) for those with low CRF and high genetic susceptibility. A similar pattern was observed in participants with low CRF and high inflammation compared with those who had high CRF and low inflammation (HR = 2.53; 95% CI: 1.83-3.48), though the interaction between CRF and inflammation did not reach statistical significance. T2D risk declined progressively with increased CRF among different inflammation categories. Conclusion: Our study reveals that genetic susceptibility may modify the association between CRF and T2D, highlighting that risk of T2D associated with genetics could benefit most from interventions on improving CRF.
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页数:9
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