Evidence map›Paper›PMID 39744623›Full record

ArticleFrontiers in immunology2024

Serum fatty acid profiles in systemic lupus erythematosus and patient reported outcomes: The Michigan Lupus Epidemiology & Surveillance (MILES) Program.

Kristen N Gilley, Jenifer I Fenton, Suzanna M Zick, Kexin Li, Lu Wang, Wendy Marder, W Joseph McCune, Raghav Jain, Sidney Herndon-Fenton, Afton L Hassett and 3 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Kristen N GilleyUniversity of Michigan, Department of Internal Medicine, Ann Arbor, MI, United States.
Jenifer I FentonMichigan State University, Department of Food Science and Human Nutrition, East Lansing, MI, United States.
Suzanna M ZickUniversity of Michigan, Department of Family Medicine, Ann Arbor, MI, United States.
Kexin LiUniversity of Michigan, Department of Biostatistics, Ann Arbor, MI, United States.
Lu WangUniversity of Michigan, Department of Biostatistics, Ann Arbor, MI, United States.
Wendy MarderUniversity of Michigan, Department of Internal Medicine, Ann Arbor, MI, United States.
W Joseph McCuneUniversity of Michigan, Department of Internal Medicine, Ann Arbor, MI, United States.
Raghav JainMichigan State University, Department of Food Science and Human Nutrition, East Lansing, MI, United States.
Sidney Herndon-FentonMichigan State University, Department of Food Science and Human Nutrition, East Lansing, MI, United States.
Afton L HassettUniversity of Michigan, Department of Anesthesiology, Ann Arbor, MI, United States.
Kamil E BarbourCenters for Disease Control and Prevention, Division of Population Health, National Center for Chronic Disease Prevention and Health Promotion, Atlanta, GA, United States.
James J PestkaMichigan State University, Department of Food Science and Human Nutrition, East Lansing, MI, United States.
Emily C SomersUniversity of Michigan, Department of Internal Medicine, Ann Arbor, MI, United States.

Funding

Michigan Institute for Clinical and Health Research (MICHR)UM1TR004404 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Julie C Lumeng · 2023 to 2026
$39.8M
Strategic Vision & Impact on Environmental HealthP30ES017885 · NIEHS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI STUART A BATTERMAN · 2011 to 2026
$21.3M
Role of alveolar macrophage in omega-3 fatty acid amelioration of silica-triggered autoimmunity.R01ES027353 · NIEHS · MICHIGAN STATE UNIVERSITY · PI Andrew Olive · 2017 to 2026
$4.8M
Immune dysfunction associated with early life heavy metal exposureK01ES019909 · NIEHS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SOMERS, EMILY CATHERINE · 2011 to 2015
$670k
NCATS NIH HHS UM1 TR004404NCCDPHP CDC HHS U01 DP003250NCCDPHP CDC HHS U01 DP006265NCCDPHP CDC HHS U01 DP006489NCCDPHP CDC HHS U58 DP001441NIEHS NIH HHS K01 ES019909NIEHS NIH HHS P30 ES017885NIEHS NIH HHS R01 ES027353
6 · The paper itself

Abstract

Introduction: Despite progress in systemic lupus erythematosus (SLE) treatment, challenges persist in medication adherence due to side effects and costs. Precision nutrition, particularly adjusting fatty acid intake, offers a cost-effective strategy for enhancing SLE management. Prior research, including our own, indicates that increased consumption of omega-3 polyunsaturated fatty acids (PUFAs) correlates with improved outcomes in SLE patients. Here we build upon these findings by investigating associations between serum fatty acids-grouped as PUFAs, monounsaturated fatty acids (MUFAs), and saturated fatty acids (SFAs)-and lupus activity, pain, and sleep disturbance. Methods: Using data from 418 participants with SLE in the Michigan Lupus Epidemiology and Surveillance (MILES) Cohort, we examined associations between serum levels of 25 fatty acids determined by GC-MS and patient-reported outcomes. Disease activity, pain, and sleep quality were assessed using standardized questionnaires. Generalized additive models and partial residual plots were utilized to examine the linearity of fatty acid effects. Variable selection was performed using Least Absolute Shrinkage and Selection Operator (LASSO), followed by multiple linear regression adjusting for sociodemographic factors. Results: Findings indicated favorable associations between ω-3 PUFAs-and, to a lesser extent, ω-6 PUFAs-and patient-reported outcomes, while MUFAs and SFAs showed unfavorable associations. Docosahexaenoic acid (DHA), an omega-3 PUFA, exhibited the most robust favorable associations across all outcomes. Additionally, the omega-3 α-linolenic acid (ALA) was linked to reduced pain, whereas eicosapentaenoic acid (EPA), another omega-3, was associated with worsened disease activity and pain. Among omega-6 PUFAs, dihomo-γ-linolenic acid (DGLA) was favorably associated with disease activity, while the omega-9 PUFA Mead acid was linked to increased pain. Discussion: These findings underscore the prospect that increased tissue levels of long-chain omega-3 PUFAs, particularly DHA, are favorably associated with SLE outcomes. Although further research is needed to establish causal relationships, existing evidence supports the role of omega-3 PUFAs in managing cardiovascular and chronic kidney disease, common SLE comorbidities. Most study participants exhibited low omega-3 PUFA status, suggesting substantial potential for improvement through targeted dietary interventions and supplementation. This study supports a potential role for precision nutrition in comprehensive SLE management, considering the impact of PUFAs, SFAs and MUFAs.

Indexed as

Fatty AcidsLupus Erythematosus, SystemicPatient Reported Outcome MeasuresAdultBiomarkersFatty Acids, Omega-3FemaleHumansMaleMichiganMiddle AgedBiomarkersFatty AcidsFatty Acids, Omega-3autoimmunedocosahexaenoic acid (DHA)monounsaturated fatty acid (MUFA)omega-3 fatty acidpainpolyunsaturated fatty acid (PUFA)saturated fatty acid (SFA)sleep

Identifiers

PMID39744623
PMCPMC11688325

What Socratic holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.