Rationale and Objectives
To investigate whether diffusion kurtosis imaging (DKI) can distinguish mild cognitive
impairment (MCI) from normal controls (NC) in aluminum (Al)-exposed workers, and to
explore the association of DKI with cognitive performance and plasma Al concentration.
Materials and Methods
28 patients with MCI and 25 NC at Al factory were enrolled in this study. All subjects
underwent conventional MRI and DKI scans. The mean kurtosis (MK), axial kurtosis (Ka),
radial kurtosis (Kr), mean diffusivity (MD) and fractional anisotropy (FA) parameters
of the hippocampus, substantia nigra, red nucleus, thalamus, anterior cingulate gyrus,
genu and crus of the corpus callosum, frontal, parietal and temporal lobe were measured.
To compare the parameters between the two groups, the Mann-Whitney rank sum test was
used. The correlation of parameter values with cognitive performance and plasma Al
concentration was analyzed using Spearman correlation analysis. The receiver operating
characteristic (ROC) curve and the Z-scores were used to evaluate the diagnostic efficacy
of each parameter.
Results
Compared with the NC group, the MK, Ka, Kr, and FA values in the MCI group were significantly
decreased, and the MD values were significantly increased (p<0.05). For the diagnosis of MCI, MK in the right hippocampus showed the largest AUC
(0.924). The MK, Kr, MD and FA values were correlated with the Montreal Cognitive
Assessment (MoCA) scores, and MK values in the right hippocampus showed the greatest
correlation with MoCA scores (r=0.744, p <0.001). Plasma Al in the MCI group was higher than that in the NC group, although
there was no significant difference in plasma Al between the two groups (p=0.057). There was no correlation between DKI parameters and plasma Al.
Conclusion
The DKI method might be a sensitive imaging biomarker to discriminate MCI from NC,
and could preliminarily assess the severity of cognitive impairment in Al-exposed
workers. MK in the right hippocampus appeared to be the best independent predictor.
The mechanism of cognitive decline is an important content of aluminum exposure research.
This study indicates that the DKI technique could provide valuable information for
the diagnosis of MCI.
Key Words
To read this article in full you will need to make a payment
Purchase one-time access:
Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online accessOne-time access price info
- For academic or personal research use, select 'Academic and Personal'
- For corporate R&D use, select 'Corporate R&D Professionals'
Subscribe:
Subscribe to Academic RadiologyAlready a print subscriber? Claim online access
Already an online subscriber? Sign in
Register: Create an account
Institutional Access: Sign in to ScienceDirect
References
- The connection between MCI and Alzheimer disease: neurocognitive clues [J].Turk J Med Sci. 2015; 45: 1137-1140https://doi.org/10.3906/sag-1404-179
- Mini-Mental State Examination (MMSE) for the early detection of dementia in people with mild cognitive impairment (MCI) [J].Cochrane Database Syst Rev. 2021; 7CD010783https://doi.org/10.1002/14651858.CD010783
- Mild cognitive impairment–beyond controversies, towards a consensus: report of the International Working Group on Mild Cognitive Impairment [J].J Intern Med. 2004; 256: 240-246https://doi.org/10.1111/j.1365-2796.2004.01380.x
- Progression from mild cognitive impairment to Alzheimer's disease: effects of sex, butyrylcholinesterase genotype, and rivastigmine treatment [J].Pharmacogenet Genomics. 2009; 19: 635-646https://doi.org/10.1097/FPC.0b013e32832f8c17
- Summary of the evidence on modifiable risk factors for cognitive decline and dementia: A population-based perspective [J].Alzheimers Dement. 2015; 11: 718-726https://doi.org/10.1016/j.jalz.2015.05.016
- Occupational exposure to aluminum and its amyloidogenic link with cognitive functions [J].J Inorg Biochem. 2014; 139: 57-64https://doi.org/10.1016/j.jinorgbio.2014.06.003
- Cognitive disorders and tau-protein expression among retired aluminum smelting workers [J].J Occup Environ Med. 2014; 56: 155-160https://doi.org/10.1097/jom.0000000000000100
- Aluminum-Induced Synaptic Plasticity Impairment via PI3K-Akt-mTOR Signaling Pathway [J].Neurotox Res. 2020; 37: 996-1008https://doi.org/10.1007/s12640-020-00165-5
- Whole brain white matter histogram analysis of diffusion tensor imaging data detects microstructural damage in mild cognitive impairment and alzheimer’s disease patients [J].J Magn Reson Imaging. 2018; 48: 767-779https://doi.org/10.1002/jmri.25947
- Review of diffusion MRI studies in chronic white matter diseases [J].Neurosci Lett. 2019; 694: 198-207https://doi.org/10.1016/j.neulet.2018.12.007
- Diffusion tensor imaging based white matter changes and antioxidant enzymes status for early identification of mild cognitive impairment [J].Int J Neurosci. 2019; 129: 209-216https://doi.org/10.1080/00207454.2018.1521401
- White matter microstructural abnormalities in amnestic mild cognitive impairment: A meta-analysis of whole-brain and ROI-based studies [J].Neurosci Biobehav Rev. 2017; 83: 405-416https://doi.org/10.1016/j.neubiorev.2017.10.026
- Patients with Mild Cognitive Impairment may be Stratified by Advanced Diffusion Metrics and Neurocognitive Testing [J].J Neuroimaging. 2019; 29: 79-84https://doi.org/10.1111/jon.12588
- White matter damage in Alzheimer disease and mild cognitive impairment: assessment with diffusion-tensor MR imaging and parallel imaging techniques [J].Radiology. 2007; 243: 483-492https://doi.org/10.1148/radiol.2432051714
- The microstructural abnormalities of cingulum was related to patients with mild cognitive impairment: a diffusion kurtosis imaging study[J].Neurol Sci. 2023; 44: 171-180https://doi.org/10.1007/s10072-022-06408-x
- Diffusional kurtosis imaging: the quantification of non-gaussian water diffusion by means of magnetic resonance imaging [J].Magn Reson Med. 2005; 53: 1432-1440https://doi.org/10.1002/mrm.20508
- Correlations between the Microstructural Changes of the Medial Temporal Cortex and Mild Cognitive Impairment in patients with Cerebral Small Vascular Disease (cSVD): aDiffusion Kurtosis Imaging Study [J].Front Neurol. 2019; 10https://doi.org/10.3389/fneur.2019.01378
- Microstructural changes in the cingulate gyrus of patients with mild cognitive impairment induced by cerebral small vessel disease [J].Neurol Res. 2021; 43: 659-667https://doi.org/10.1080/01616412.2021.1910903
- Differentiating between Alzheimer's disease, amnestic mild cognitive impairment, and normal aging via diffusion kurtosis imaging [J].Neural Regen Res. 2019; 14: 2141-2146https://doi.org/10.4103/1673-5374.262594
- The diagnosis of mild cognitive impairment due to Alzheimer's disease: recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease [J].Alzheimers Dement. 2011; 7: 270-279https://doi.org/10.1016/j.jalz.2011.03.008
- Non-Gaussian diffusion MRI assessment of brain microstructure in mild cognitive impairment and Alzheimer's disease [J].Magn Reson Imaging. 2013; 31: 840-846https://doi.org/10.1016/j.mri.2013.02.008
- A meta-analysis of diffusion tensor imaging in mild cognitive impairment and Alzheimer’s disease [J].Neurobiol Aging. 2011; 32: 2322,e5-18https://doi.org/10.1016/j.neurobiolaging.2010.05.019
- Development of a superior frontal-intraparietal network for visuo-spatial working memory [J].Neuropsychologia. 2006; 44: 2171-2177https://doi.org/10.1016/j.neuropsychologia.2005.11.019
- White matter alterations in early-stage Alzheimer's disease: A tract-specific study [J].Alzheimers Dement (Amst). 2019; 11: 576-587https://doi.org/10.1016/j.dadm.2019.06.003
- A geometric analysis of diffusion tensor measurements of the human brain [J].Magn Reson Med. 2000; 44: 283-291https://doi.org/10.1002/1522-2594(200008)44:2<283::aid-mrm16>3.0.co;2-v
- Microstructural changes observed with DKI in a transgenic Huntington rat model: evidence for abnormal neurodevelopment [J].Neuroimage. 2012; 59: 957-967https://doi.org/10.1016/j.neuroimage.2011.08.062
- Non-Gaussian diffusion alterations on diffusion kurtosis imaging in patients with early Alzheimer's disease [J].Neurosci Lett. 2016; 616: 11-18https://doi.org/10.1016/j.neulet.2016.01.021
- Effect of cerebral spinal fluid suppression for diffusional kurtosis imaging [J].J Magn Reson Imaging. 2013; 37: 365-371https://doi.org/10.1002/jmri.23840
- Involvement of altered cytoskeletal protein phosphorylation in aluminum-induced CNS dysfunction [J].J Biochem Toxicol. 1996; 11: 227-233https://doi.org/10.1002/(sici)1522-7146(1996)11:5<227::Aid-jbt3>3.0.Co;2-m
- Relationship between hippocampal volume and memory ability in healthy individuals across the lifespan: review and meta-analysis [J].Neuropsychologia. 2004; 42: 1394-1413https://doi.org/10.1016/j.neuropsychologia.2004.04.006
- First magenetic resonance imaging studies on aluminium maltolate-treated aged New Zealand rabbits:an Alzheimer's animal mode [J].Psychogeriatrics. 2016; 16: 263-267https://doi.org/10.1111/psyg.12158
- Vector trace cells in the subiculum of the hippocampal formation [J].Nat Neurosci. 2021; 24: 266-275https://doi.org/10.1038/s41593-020-00761-w
- Entry and Deposit of Aluminum in the Brain [J].Adv Exp Med Biol. 2018; 1091: 39-51https://doi.org/10.1007/978-981-13-1370-7_3
- Aluminum impairs cognitive function by activating DDX3X-NLRP3-mediated pyroptosis signaling pathway [J].Food and Chemical Toxicol. 2021; 157112591https://doi.org/10.1016/j.fct.2021.112591
- Neurocognitive effects in welders exposed to aluminium [J].Toxicol Ind Health. 2014; 30: 347-356https://doi.org/10.1177/0748233712456062
- Neurotoxic effects of aluminium among foundry workers and Alzheimer's disease [J].Neurotoxicology. 2002; 23: 761-774https://doi.org/10.1016/s0161-813x(02)00097-9
- Occupational exposure to aluminum and its biomonitoring in perspective [J].Crit Rev Toxicol. 2012; 42: 827-853https://doi.org/10.3109/10408444.2012.725027
- Occupational aluminum exposure: evidence in support of its neurobehavioral impact [J].Neurotoxicology. 2007; 28: 1068-1078https://doi.org/10.1016/j.neuro.2007.07.001
- Monitoring mild cognitive impairment of workers exposed to occupational aluminium based on quantitative susceptibility mapping[J].Clin Radiol. 2022; 77: 840-847https://doi.org/10.1016/j.crad.2022.06.007
- Blood glucose mediated the effects of cognitive function impairment related to aluminum exposure in Chinese aluminum smelting workers [J].Neurotoxicology. 2022; 91: 282-289https://doi.org/10.1016/j.neuro.2022.06.001
- Cross-sectional study based on occupational aluminium exposure population[J].Environ Toxicol Pharmacol. 2021; 83103581https://doi.org/10.1016/j.etap.2020.103581
Article info
Publication history
Published online: January 21, 2023
Accepted:
December 2,
2022
Received in revised form:
December 2,
2022
Received:
August 28,
2022
Publication stage
In Press Corrected ProofIdentification
Copyright
© 2023 Published by Elsevier Inc. on behalf of The Association of University Radiologists.