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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....

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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.
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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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