TY - JOUR
T1 - A characteristic N-glycopeptide signature associated with diabetic cognitive impairment identified in a longitudinal cohort study
AU - Miura, Yuri
AU - Tsumoto, Hiroki
AU - Masui, Yukie
AU - Inagaki, Hiroki
AU - Ogawa, Madoka
AU - Ideno, Yuta
AU - Kawakami, Kyojiro
AU - Umezawa, Keitaro
AU - Kabayama, Mai
AU - Akagi, Yuya
AU - Akasaka, Hiroshi
AU - Yamamoto, Koichi
AU - Rakugi, Hiromi
AU - Ishizaki, Tatsuro
AU - Arai, Yasumichi
AU - Ikebe, Kazunori
AU - Kamide, Kei
AU - Gondo, Yasuyuki
AU - Endo, Tamao
N1 - Funding Information:
This work was supported by JSPS KAKENHI (Japan) [grant numbers 19K11736 and 17K19950 ], the Mitsui Sumitomo Insurance Welfare Foundation (Japan) , the Uehara Memorial Foundation (Japan) [to YMiura], and JSPS KAKENHI [grant numbers 26310104 (to YG), 15H05025 (to KI), 20H03923 (to TI), and 15K04176 (to YMasui)]. The authors would like to thank Mr. Yoshikawa (Infocom Co.) for technical assistance with the OPLS.
Publisher Copyright:
© 2023 Elsevier B.V.
PY - 2023/4
Y1 - 2023/4
N2 - Background: Identifying a biomarker for the decline in cognitive function in patients with diabetes is important. Therefore, we aimed to identify the N-glycopeptides on plasma proteins associated with diabetic cognitive impairment in participants in a longitudinal study using N-glycoproteomics. Methods: We used samples from the 3-year SONIC (Septuagenarians, Octogenarians, Nonagenarians Investigation with Centenarians) longitudinal cohort study of older Japanese people in the general population. First, we placed the participants with diabetes into two groups: those that did or did not have cognitive decline over a 6-year period. Next, their plasma protein profiles were compared between baseline and the 6-year time point using two-dimensional fluorescence difference gel electrophoresis. Finally, an N-glycoproteomic study of the focused proteins was performed using an enrichment technique and liquid chromatography-tandem mass spectrometry. Results: Approximately 500 N-glycopeptides, derived from 18 proteins, were identified in each sample, from among which we identified the N-glycopeptides that were associated with diabetic cognitive impairment using multivariate analysis. We found that N-glycopeptides with sialylated tri- or tetra-antennary glycans on alpha-2-macroglobulin, clusterin, serum paraoxonase/arylesterase 1, and haptoglobin were less abundant, whereas 3-sialylated tri-antennary N-glycopeptides on serotransferrin were more abundant. Conclusion: N-glycopeptides with sialylated multi-antennary glycans comprise a characteristic signature associated with diabetic cognitive impairment. General significance: The characterized N-glycopeptides represent potential biomarker candidates for diabetic cognitive impairment.
AB - Background: Identifying a biomarker for the decline in cognitive function in patients with diabetes is important. Therefore, we aimed to identify the N-glycopeptides on plasma proteins associated with diabetic cognitive impairment in participants in a longitudinal study using N-glycoproteomics. Methods: We used samples from the 3-year SONIC (Septuagenarians, Octogenarians, Nonagenarians Investigation with Centenarians) longitudinal cohort study of older Japanese people in the general population. First, we placed the participants with diabetes into two groups: those that did or did not have cognitive decline over a 6-year period. Next, their plasma protein profiles were compared between baseline and the 6-year time point using two-dimensional fluorescence difference gel electrophoresis. Finally, an N-glycoproteomic study of the focused proteins was performed using an enrichment technique and liquid chromatography-tandem mass spectrometry. Results: Approximately 500 N-glycopeptides, derived from 18 proteins, were identified in each sample, from among which we identified the N-glycopeptides that were associated with diabetic cognitive impairment using multivariate analysis. We found that N-glycopeptides with sialylated tri- or tetra-antennary glycans on alpha-2-macroglobulin, clusterin, serum paraoxonase/arylesterase 1, and haptoglobin were less abundant, whereas 3-sialylated tri-antennary N-glycopeptides on serotransferrin were more abundant. Conclusion: N-glycopeptides with sialylated multi-antennary glycans comprise a characteristic signature associated with diabetic cognitive impairment. General significance: The characterized N-glycopeptides represent potential biomarker candidates for diabetic cognitive impairment.
KW - Cognitive impairment
KW - Diabetes
KW - Liquid chromatography-tandem mass spectrometry
KW - Longitudinal cohort study
KW - N-glycoproteomics
KW - Proteomics
UR - http://www.scopus.com/inward/record.url?scp=85147830387&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85147830387&partnerID=8YFLogxK
U2 - 10.1016/j.bbagen.2023.130316
DO - 10.1016/j.bbagen.2023.130316
M3 - Article
C2 - 36720372
AN - SCOPUS:85147830387
SN - 0006-3002
VL - 1867
JO - Biochimica et Biophysica Acta - General Subjects
JF - Biochimica et Biophysica Acta - General Subjects
IS - 4
M1 - 130316
ER -