Fasting glucose variability and risk of dementia in Parkinson's disease: a 9-year longitudinal follow-up study of a nationwide cohort

被引:0
|
作者
Kang, Sung Hoon [1 ]
Choi, Yunjin [2 ]
Chung, Su Jin [3 ]
Moon, Seok-Joo [4 ]
Kim, Chi Kyung [1 ]
Kim, Ji Hyun [1 ]
Oh, Kyungmi [1 ]
Yoon, Joon Shik [5 ]
Seo, Sang Won [6 ,7 ]
Cho, Geum Joon [8 ]
Koh, Seong-Beom [1 ]
机构
[1] Korea Univ, Coll Med, Dept Neurol, Guro Hosp, Seoul, South Korea
[2] Korea Univ, Guro Hosp, Coll Med, Biomed Res Inst, Seoul, South Korea
[3] Hanyang Univ, Coll Med, Myongji Hosp, Dept Neurol, Goyang, South Korea
[4] Korea Univ, Coll Med, Guro Hosp, Smart Healthcare Ctr, Seoul, South Korea
[5] Korea Univ, Guro Hosp, Dept Phys Med & Rehabil, Seoul, South Korea
[6] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Neurol, Seoul, South Korea
[7] Alzheimers Dis Convergence Res Ctr, Samsung Med Ctr, Seoul, South Korea
[8] Korea Univ, Coll Med, Dept Obstet & Gynecol, Guro Hosp, Seoul, South Korea
来源
基金
新加坡国家研究基金会;
关键词
Parkinson' s disease; Parkinson's disease dementia; glucose variability; fasting glucose; risk factors; DIABETES-MELLITUS; OXIDATIVE STRESS; ASSOCIATION; ALZHEIMERS; EXPRESSION;
D O I
10.3389/fnagi.2023.1292524
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Background: Diabetes is associated with an increased risk of Parkinson's disease dementia (PDD); however, it is unknown whether this association is dependent on continuous hyperglycemia, hypoglycemic events, or glycemic variability. We aimed to investigate the relationship between visit-to-visit fasting glucose variability and PDD development in patients with Parkinson's disease (PD). Methods: Using data from the Korean National Health Insurance Service, we examined 9,264 patients aged >= 40 years with de novo Parkinson's disease (PD) who underwent >= 3 health examinations and were followed up until December 2019. Glucose variability was measured using the coefficient of variation, variability independent of the mean, and average real variability. Fine and Gray competing regression analysis was performed to determine the effect of glucose variability on incident PDD. Results: During the 9.5-year follow-up period, 1,757 of 9,264 (19.0%) patients developed PDD. Patients with a higher visit-to-visit glucose variability had a higher risk of future PDD. In the multivariable adjusted model, patients with PD in the highest quartile (subdistribution hazard ratio [SHR] = 1.50, 95% CI 1.19 to 1.88), quartile 3 (SHR = 1.29, 95% CI 1.02 to 1.62), and quartile 2 (SHR = 1.30, 95% CI 1.04 to 1.63) were independently associated with a higher risk of PDD than those in the lowest quartile. Conclusion: We highlighted the effect of long-term glucose variability on the development of PDD in patients with PD. Furthermore, our findings suggest that preventive measures for constant glucose control may be necessary to prevent PDD.
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页数:7
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