Evidence map›Paper›PMID 36567420›Full record

ArticleSleep & breathing = Schlaf & Atmung2023

Correlation between nocturnal intermittent hypoxemia and mild cognitive impairment in the older adult and the role of BDNF Val66Met polymorphism: a hospital-based cross-sectional study.

L H Deng, J X Geng, Q Xue, J Jiang, L X Chen, J T Wang

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Article in Sleep & breathing = Schlaf & Atmung, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

L H DengDepartment of Geriatrics, Peking University People's Hospital, No. 11 Xizhimen South Street, Xicheng District, 100044, Beijing, People's Republic of China.
J X GengPeking University Health Science Center, Beijing, China.
Q XueDepartment of Geriatrics, Peking University People's Hospital, No. 11 Xizhimen South Street, Xicheng District, 100044, Beijing, People's Republic of China.
J JiangDepartment of Geriatrics, Peking University People's Hospital, No. 11 Xizhimen South Street, Xicheng District, 100044, Beijing, People's Republic of China.
L X ChenDepartment of Geriatrics, Peking University People's Hospital, No. 11 Xizhimen South Street, Xicheng District, 100044, Beijing, People's Republic of China.
J T WangDepartment of Geriatrics, Peking University People's Hospital, No. 11 Xizhimen South Street, Xicheng District, 100044, Beijing, People's Republic of China. wangjingtong@pkuph.edu.cn.ORCID 0000-0003-0878-2054
Peking University · CN

Funding

Beijing Municipal Science and Technology Committee D171100008217005
6 · The paper itself

Abstract

purposeTo explore the prevalence of nocturnal intermittent hypoxemia (NIH) in a tertiary hospital geriatric department and the relationship between NIH and mild cognitive impairment (MCI) in older adults, and to examine the role of brain-derived neurotrophic factor (BDNF) Val66Met polymorphism.

methodsOlder adults aged ≥ 60 were enrolled. NIH and cognitive assessments were conducted. BDNF concentrations and BDNF Val66Met polymorphism were detected for a preliminary exploration of the possible mechanism of the process.

resultsOf 325 older adults enrolled, 157 (48%) had NIH and were further divided into mild, moderate, and severe NIH groups according to their oxygen desaturation of ≥ 4% per hour of sleep (ODI4). MCI detection rate in the four groups gradually increased, and the differences were statistically significant (chi-square = 4.457, P = 0.035). ODI4 was negatively correlated with MoCA score in all participants (r =  - 0.115, P = 0.039) and patients with NIH (r =  - 0.199, P = 0.012). After adjusting for sex, age, and cardiovascular risk factors, NIH and MCI remained independently associated (OR = 3.13, 95% CI 1.03-9.53, P = 0.045). BDNF levels were positively correlated with MoCA score (r = 0.169, P = 0.028) and negatively correlated with nocturnal average oxygen saturation in patients with NIH (r =  - 0.288, P = 0.008). Older adults with different BDNF Val66Met genotypes did not show significant differences in MCI rate and BDNF levels (P > 0.05).

conclusionThe older adults with NIH have a higher MCI detection rate. BDNF levels may be a potential biomarker for cognitive dysfunction in patients with NIH.

Indexed as

Brain-Derived Neurotrophic FactorCognitive DysfunctionAgedCross-Sectional StudiesGenotypeHospitalsHumansHypoxiaBDNF protein, humanBrain-Derived Neurotrophic FactorBrain-derived neurotrophic factorMild cognitive impairmentNocturnal intermittent hypoxemiaOxygen desaturation indexVal66Met polymorphism

Identifiers

PMID36567420
OpenAlexW4312195472

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.