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Serum lipidomic determinants of human diabetic neuropathy in type 2 diabetes
OBJECTIVE: The serum lipidomic profile associated with neuropathy in type 2 diabetes is not well understood. Obesity and dyslipidemia are known neuropathy risk factors, suggesting lipid profiles early during type 2 diabetes may identify individuals who develop neuropathy later in the disease course....
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9463947/ https://www.ncbi.nlm.nih.gov/pubmed/35923113 http://dx.doi.org/10.1002/acn3.51639 |
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author | Afshinnia, Farsad Reynolds, Evan L. Rajendiran, Thekkelnaycke M. Soni, Tanu Byun, Jaeman Savelieff, Masha G. Looker, Helen C. Nelson, Robert G. Michailidis, George Callaghan, Brian C. Pennathur, Subramaniam Feldman, Eva L. |
author_facet | Afshinnia, Farsad Reynolds, Evan L. Rajendiran, Thekkelnaycke M. Soni, Tanu Byun, Jaeman Savelieff, Masha G. Looker, Helen C. Nelson, Robert G. Michailidis, George Callaghan, Brian C. Pennathur, Subramaniam Feldman, Eva L. |
author_sort | Afshinnia, Farsad |
collection | PubMed |
description | OBJECTIVE: The serum lipidomic profile associated with neuropathy in type 2 diabetes is not well understood. Obesity and dyslipidemia are known neuropathy risk factors, suggesting lipid profiles early during type 2 diabetes may identify individuals who develop neuropathy later in the disease course. This retrospective cohort study examined lipidomic profiles 10 years prior to type 2 diabetic neuropathy assessment. METHODS: Participants comprised members of the Gila River Indian community with type 2 diabetes (n = 69) with available stored serum samples and neuropathy assessment 10 years later using the combined Michigan Neuropathy Screening Instrument (MNSI) examination and questionnaire scores. A combined MNSI index was calculated from examination and questionnaire scores. Serum lipids (435 species from 18 classes) were quantified by mass spectrometry. RESULTS: The cohort included 17 males and 52 females with a mean age of 45 years (SD = 9 years). Participants were stratified as with (high MNSI index score > 2.5407) versus without neuropathy (low MNSI index score ≤ 2.5407). Significantly decreased medium‐chain acylcarnitines and increased total free fatty acids, independent of chain length and saturation, in serum at baseline associated with incident peripheral neuropathy at follow‐up, that is, participants had high MNSI index scores, independent of covariates. Participants with neuropathy also had decreased phosphatidylcholines and increased lysophosphatidylcholines at baseline, independent of chain length and saturation. The abundance of other lipid classes did not differ significantly by neuropathy status. INTERPRETATION: Abundance differences in circulating acylcarnitines, free fatty acids, phosphatidylcholines, and lysophosphatidylcholines 10 years prior to neuropathy assessment are associated with neuropathy status in type 2 diabetes. |
format | Online Article Text |
id | pubmed-9463947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94639472022-09-13 Serum lipidomic determinants of human diabetic neuropathy in type 2 diabetes Afshinnia, Farsad Reynolds, Evan L. Rajendiran, Thekkelnaycke M. Soni, Tanu Byun, Jaeman Savelieff, Masha G. Looker, Helen C. Nelson, Robert G. Michailidis, George Callaghan, Brian C. Pennathur, Subramaniam Feldman, Eva L. Ann Clin Transl Neurol Research Articles OBJECTIVE: The serum lipidomic profile associated with neuropathy in type 2 diabetes is not well understood. Obesity and dyslipidemia are known neuropathy risk factors, suggesting lipid profiles early during type 2 diabetes may identify individuals who develop neuropathy later in the disease course. This retrospective cohort study examined lipidomic profiles 10 years prior to type 2 diabetic neuropathy assessment. METHODS: Participants comprised members of the Gila River Indian community with type 2 diabetes (n = 69) with available stored serum samples and neuropathy assessment 10 years later using the combined Michigan Neuropathy Screening Instrument (MNSI) examination and questionnaire scores. A combined MNSI index was calculated from examination and questionnaire scores. Serum lipids (435 species from 18 classes) were quantified by mass spectrometry. RESULTS: The cohort included 17 males and 52 females with a mean age of 45 years (SD = 9 years). Participants were stratified as with (high MNSI index score > 2.5407) versus without neuropathy (low MNSI index score ≤ 2.5407). Significantly decreased medium‐chain acylcarnitines and increased total free fatty acids, independent of chain length and saturation, in serum at baseline associated with incident peripheral neuropathy at follow‐up, that is, participants had high MNSI index scores, independent of covariates. Participants with neuropathy also had decreased phosphatidylcholines and increased lysophosphatidylcholines at baseline, independent of chain length and saturation. The abundance of other lipid classes did not differ significantly by neuropathy status. INTERPRETATION: Abundance differences in circulating acylcarnitines, free fatty acids, phosphatidylcholines, and lysophosphatidylcholines 10 years prior to neuropathy assessment are associated with neuropathy status in type 2 diabetes. John Wiley and Sons Inc. 2022-08-03 /pmc/articles/PMC9463947/ /pubmed/35923113 http://dx.doi.org/10.1002/acn3.51639 Text en © 2022 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Afshinnia, Farsad Reynolds, Evan L. Rajendiran, Thekkelnaycke M. Soni, Tanu Byun, Jaeman Savelieff, Masha G. Looker, Helen C. Nelson, Robert G. Michailidis, George Callaghan, Brian C. Pennathur, Subramaniam Feldman, Eva L. Serum lipidomic determinants of human diabetic neuropathy in type 2 diabetes |
title | Serum lipidomic determinants of human diabetic neuropathy in type 2 diabetes |
title_full | Serum lipidomic determinants of human diabetic neuropathy in type 2 diabetes |
title_fullStr | Serum lipidomic determinants of human diabetic neuropathy in type 2 diabetes |
title_full_unstemmed | Serum lipidomic determinants of human diabetic neuropathy in type 2 diabetes |
title_short | Serum lipidomic determinants of human diabetic neuropathy in type 2 diabetes |
title_sort | serum lipidomic determinants of human diabetic neuropathy in type 2 diabetes |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9463947/ https://www.ncbi.nlm.nih.gov/pubmed/35923113 http://dx.doi.org/10.1002/acn3.51639 |
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