Newer glucose-lowering drugs and risk of dementia: A systematic review and meta-analysis of observational studies

被引:58
作者
Tang, Huilin [1 ]
Shao, Hui [1 ,2 ]
Shaaban, C. Elizabeth [3 ]
Yang, Keming [4 ,5 ]
Brown, Joshua [1 ,2 ]
Anton, Stephen [6 ,7 ]
Wu, Yonghui [8 ]
Bress, Adam [9 ]
Donahoo, William T. [10 ]
DeKosky, Steven T. [11 ]
Bian, Jiang [8 ]
Guo, Jingchuan [1 ,2 ,12 ]
机构
[1] Univ Florida, Dept Pharmaceut Outcomes & Policy, Coll Pharm, Gainesville, FL USA
[2] Univ Florida, Ctr Drug Evaluat & Safety, Gainesville, FL USA
[3] Univ Pittsburgh, Sch Publ Hlth, Dept Epidemiol, Pittsburgh, PA USA
[4] Massachusetts Gen Hosp, Dept Med, Clin & Translat Epidemiol Unit, Boston, MA USA
[5] Harvard Med Sch, Boston, MA USA
[6] Univ Florida, Coll Med, Dept Aging & Geriatr Res, Gainesville, FL USA
[7] Univ Florida, Coll Publ Hlth & Hlth Profess, Dept Clin & Hlth Psychol, Gainesville, FL USA
[8] Univ Florida, Coll Med, Dept Hlth Outcomes & Biomed Informat, Gainesville, FL USA
[9] Univ Utah, Dept Populat Hlth Sci, Div Hlth Syst Innovat & Res, Salt Lake City, UT USA
[10] Univ Florida, Coll Med, Div Endocrinol Diabet & Metab, Gainesville, FL USA
[11] Univ Florida, Coll Med, Dept Neurol, Gainesville, FL USA
[12] Univ Florida, Dept Pharmaceut Outcomes & Policy, Coll Pharm, Gainesville, FL 32610 USA
基金
美国国家卫生研究院;
关键词
dementia; DPP-4; inhibitors; GLP-1RAs; SGLT2; type; 2; diabetes; COGNITIVE IMPAIRMENT; DPP-4; INHIBITOR; DIABETES-MELLITUS; DISEASE; CANAGLIFLOZIN; LIRAGLUTIDE; MECHANISMS; PATHOLOGY; OBESITY;
D O I
10.1111/jgs.18306
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: Preclinical studies have suggested potential beneficial effects of newer glucose-lowering drugs (GLDs) including dipeptidyl peptidase (DPP)-4 inhibitors, glucagon-like peptide-1 receptor agonists (GLP-1RAs), and sodium glucose co-transporter-2 (SGLT2) inhibitors, in protecting humans against cognitive decline and dementia. However, population studies aiming to demonstrate such cognitive benefits from newer GLDs have produced mixed findings. This meta-analysis aimed to evaluate the association between newer GLDs and risk of dementia in adults with type 2 diabetes (T2D).Methods: Electronic databases were searched up to March 11, 2022 to include observational studies that examined the association between DPP-4 inhibitors, GLP-1RAs, and SGLT2 inhibitors and risk of dementia (including all-cause dementia, Alzheimer's disease [AD], and vascular dementia [VD]) in people with T2D. We conducted a random-effects meta-analysis to calculate the relative risk (RR) with 95% confidence interval (CI) for each class of newer GLD.Results: Ten studies (from nine articles) involving 819,511 individuals with T2D were included. Three studies found that SGLT2 inhibitor users had a lower risk of all-cause dementia than non-SGLT2 inhibitor users (RR, 0.62; 95% CI, 0.39-0.97). Five studies found that users versus nonusers of GLP-1RAs were associated with a significant reduction in the risk of all-cause dementia (RR, 0.72; 95% CI, 0.54-0.97). However, a meta-analysis for AD and VD was unavailable for SGLT2 inhibitors and GLP-1RAs because only one study was included for each drug. In seven studies, users vs. nonusers of DPP-4 inhibitors were significantly associated with a decreased risk of all-cause dementia (RR, 0.84; 95% CI, 0.74-0.94) and VD (RR, 0.59; 95% CI, 0.47-0.75) but not AD (RR, 0.82; 95% CI, 0.63-1.08).Conclusion: Newer GLDs were associated with a decreased risk of all-cause dementia in people with T2D. Because of the observational nature and significant heterogeneity between studies, the results should be interpreted with caution. Further research is warranted to confirm our findings.
引用
收藏
页码:2096 / 2106
页数:11
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