Protective effects of APOE e2 against disease progression in subcortical vascular mild cognitive impairment patients: A three-year longitudinal study
Abstract Although the association between apolipoprotein E (APOE) genotype and disease progression is well characterized in patients with Alzheimer’s disease, such a relationship is unknown in patients with subcortical vascular cognitive impairment. We evaluated whether APOE genotype is associated w...
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oai:doaj.org-article:5c4ad772c0a44db09bc1dc28574a45272021-12-02T16:06:42ZProtective effects of APOE e2 against disease progression in subcortical vascular mild cognitive impairment patients: A three-year longitudinal study10.1038/s41598-017-02046-y2045-2322https://doaj.org/article/5c4ad772c0a44db09bc1dc28574a45272017-05-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-02046-yhttps://doaj.org/toc/2045-2322Abstract Although the association between apolipoprotein E (APOE) genotype and disease progression is well characterized in patients with Alzheimer’s disease, such a relationship is unknown in patients with subcortical vascular cognitive impairment. We evaluated whether APOE genotype is associated with disease progression in subcortical vascular mild cognitive impairment (svMCI) patients. We prospectively recruited 72 svMCI patients (19 APOE4 carriers, 42 APOE3 homozygotes, and 11 APOE2 carriers). Patients were annually followed-up with brain MRI and neuropsychological tests for three years and underwent a second Pittsburgh compound B (PiB)-PET at a mean interval of 32.3 months. Amyloid-ß burden was quantified by PiB standardized uptake value ratio (SUVR), and the amount of small vessel disease was quantified by number of lacune and small vessel disease score on MRI. We also measured cortical thickness. During the three years of follow-up, compared to the APOE3 homozygotes, there was less increase in PiB SUVR among APOE2 carriers (p = 0.023), while the APOE genotype did not show significant effects on small vessel disease progression. APOE2 carriers also showed less cortical thinning (p = 0.023) and a slower rate of cognitive decline (p = 0.009) compared to those with APOE3 homozygotes. Our findings suggest that, in svMCI patients, APOE2 has protective effects against amyloid-ß accumulation, cortical thinning, and cognitive decline.Yeo Jin KimSang Won SeoSeong Beom ParkJin Ju YangJin San LeeJuyoun LeeYoung Kyoung JangSung Tae KimKyung-Han LeeJong Min LeeJae-Hong LeeJae Seung KimDuk L. NaHee Jin KimNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-8 (2017) |
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Medicine R Science Q Yeo Jin Kim Sang Won Seo Seong Beom Park Jin Ju Yang Jin San Lee Juyoun Lee Young Kyoung Jang Sung Tae Kim Kyung-Han Lee Jong Min Lee Jae-Hong Lee Jae Seung Kim Duk L. Na Hee Jin Kim Protective effects of APOE e2 against disease progression in subcortical vascular mild cognitive impairment patients: A three-year longitudinal study |
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Abstract Although the association between apolipoprotein E (APOE) genotype and disease progression is well characterized in patients with Alzheimer’s disease, such a relationship is unknown in patients with subcortical vascular cognitive impairment. We evaluated whether APOE genotype is associated with disease progression in subcortical vascular mild cognitive impairment (svMCI) patients. We prospectively recruited 72 svMCI patients (19 APOE4 carriers, 42 APOE3 homozygotes, and 11 APOE2 carriers). Patients were annually followed-up with brain MRI and neuropsychological tests for three years and underwent a second Pittsburgh compound B (PiB)-PET at a mean interval of 32.3 months. Amyloid-ß burden was quantified by PiB standardized uptake value ratio (SUVR), and the amount of small vessel disease was quantified by number of lacune and small vessel disease score on MRI. We also measured cortical thickness. During the three years of follow-up, compared to the APOE3 homozygotes, there was less increase in PiB SUVR among APOE2 carriers (p = 0.023), while the APOE genotype did not show significant effects on small vessel disease progression. APOE2 carriers also showed less cortical thinning (p = 0.023) and a slower rate of cognitive decline (p = 0.009) compared to those with APOE3 homozygotes. Our findings suggest that, in svMCI patients, APOE2 has protective effects against amyloid-ß accumulation, cortical thinning, and cognitive decline. |
format |
article |
author |
Yeo Jin Kim Sang Won Seo Seong Beom Park Jin Ju Yang Jin San Lee Juyoun Lee Young Kyoung Jang Sung Tae Kim Kyung-Han Lee Jong Min Lee Jae-Hong Lee Jae Seung Kim Duk L. Na Hee Jin Kim |
author_facet |
Yeo Jin Kim Sang Won Seo Seong Beom Park Jin Ju Yang Jin San Lee Juyoun Lee Young Kyoung Jang Sung Tae Kim Kyung-Han Lee Jong Min Lee Jae-Hong Lee Jae Seung Kim Duk L. Na Hee Jin Kim |
author_sort |
Yeo Jin Kim |
title |
Protective effects of APOE e2 against disease progression in subcortical vascular mild cognitive impairment patients: A three-year longitudinal study |
title_short |
Protective effects of APOE e2 against disease progression in subcortical vascular mild cognitive impairment patients: A three-year longitudinal study |
title_full |
Protective effects of APOE e2 against disease progression in subcortical vascular mild cognitive impairment patients: A three-year longitudinal study |
title_fullStr |
Protective effects of APOE e2 against disease progression in subcortical vascular mild cognitive impairment patients: A three-year longitudinal study |
title_full_unstemmed |
Protective effects of APOE e2 against disease progression in subcortical vascular mild cognitive impairment patients: A three-year longitudinal study |
title_sort |
protective effects of apoe e2 against disease progression in subcortical vascular mild cognitive impairment patients: a three-year longitudinal study |
publisher |
Nature Portfolio |
publishDate |
2017 |
url |
https://doaj.org/article/5c4ad772c0a44db09bc1dc28574a4527 |
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