Evidence map›Paper›PMID 38609525›Full record

ArticleNature aging2024

A lipidome landscape of aging in mice.

Hiroshi Tsugawa, Tomoaki Ishihara, Kota Ogasa, Seigo Iwanami, Aya Hori, Mikiko Takahashi, Yutaka Yamada, Naoko Satoh-Takayama, Hiroshi Ohno, Aki Minoda and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature aging, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
11.2field-weighted citation impact, top 1% of its field
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

36 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Metabolomic Profiling ofJournal of fungi (Basel, Switzerland) · 2026
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  10. Purine salvage pathway protects CD8Nature immunology · 2026
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  13. The Microbiome Modulates Corneal Wound Healing via the Induction of Cholesterol Sulfotransferase Pathway.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  14. Article
  15. Article
  16. Article
  17. Improving our understanding of the biology of aging: findings from the Age-It Research Program.The journals of gerontology. Series B, Psychological sciences and social sciences · 2025
    Article
  18. Article
  19. Article
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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

11 authors at 6 institutions in 2 countries.

Hiroshi TsugawaLaboratory for Metabolomics, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan. htsugawa@go.tuat.ac.jp.ORCID http://orcid.org/0000-0002-2015-3958
Tomoaki IshiharaLaboratory for Metabolomics, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.ORCID http://orcid.org/0009-0005-0037-7443
Kota OgasaDivision of Physiological Chemistry and Metabolism, Graduate School of Pharmaceutical Sciences, Keio University, Tokyo, Japan.
Seigo IwanamiDivision of Physiological Chemistry and Metabolism, Graduate School of Pharmaceutical Sciences, Keio University, Tokyo, Japan.
Aya HoriLaboratory for Metabolomics, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Mikiko TakahashiMetabolome Informatics Research Team, RIKEN Center for Sustainable Resource Science, Yokohama, Japan.ORCID http://orcid.org/0000-0002-4529-2284
Yutaka YamadaMetabolome Informatics Research Team, RIKEN Center for Sustainable Resource Science, Yokohama, Japan.
Naoko Satoh-TakayamaLaboratory for Intestinal Ecosystem, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Hiroshi OhnoLaboratory for Intestinal Ecosystem, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.ORCID http://orcid.org/0000-0001-8776-9661
Aki MinodaLaboratory for Cellular Epigenomics, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Makoto AritaLaboratory for Metabolomics, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan. marita@keio.jp.ORCID http://orcid.org/0000-0001-9902-0463
Keio University · JPRIKEN Center for Integrative Medical Sciences · JPRIKEN Center for Sustainable Resource Science · JPNagasaki International University · JPRadboud University Nijmegen · NLYokohama City University Medical Center · JP

Funding

Japan Agency for Medical Research and Development (AMED) 21wm0325036h0001Japan Agency for Medical Research and Development (AMED) 22ae0121036h0002Japan Agency for Medical Research and Development (AMED) JP15dm0207001Japan Agency for Medical Research and Development (AMED) JP22zf0127007MEXT | Japan Society for the Promotion of Science (JSPS) 15H05897MEXT | Japan Society for the Promotion of Science (JSPS) 15H05898MEXT | Japan Society for the Promotion of Science (JSPS) 20H00495MEXT | Japan Society for the Promotion of Science (JSPS) 21K18216MEXT | Japan Society for the Promotion of Science (JSPS) 22K11718MEXT | JST | Exploratory Research for Advanced Technology (ERATO) JPMJER2101MEXT | JST | National Bioscience Database Center (NBDC) JPMJND2305
6 · The paper itself

Abstract

Understanding the molecular mechanisms of aging is crucial for enhancing healthy longevity. We conducted untargeted lipidomics across 13 biological samples from mice at various life stages (2, 12, 19 and 24 months) to explore the potential link between aging and lipid metabolism, considering sex (male or female) and microbiome (specific pathogen-free or germ-free) dependencies. By analyzing 2,704 molecules from 109 lipid subclasses, we characterized common and tissue-specific lipidome alterations associated with aging. For example, the levels of bis(monoacylglycero)phosphate containing polyunsaturated fatty acids increased in various organs during aging, whereas the levels of other phospholipids containing saturated and monounsaturated fatty acids decreased. In addition, we discovered age-dependent sulfonolipid accumulation, absent in germ-free mice, correlating with Alistipes abundance determined by 16S ribosomal RNA gene amplicon sequencing. In the male kidney, glycolipids such as galactosylceramides, galabiosylceramides (Gal2Cer), trihexosylceramides (Hex3Cer), and mono- and digalactosyldiacylglycerols were detected, with two lipid classes-Gal2Cer and Hex3Cer-being significantly enriched in aged mice. Integrated analysis of the kidney transcriptome revealed uridine diphosphate galactosyltransferase 8A (UGT8a), alkylglycerone phosphate synthase and fatty acyl-coenzyme A reductase 1 as potential enzymes responsible for the male-specific glycolipid biosynthesis in vivo, which would be relevant to sex dependency in kidney diseases. Inhibiting UGT8 reduced the levels of these glycolipids and the expression of inflammatory cytokines in the kidney. Our study provides a valuable resource for clarifying potential links between lipid metabolism and aging.

Indexed as

AgingLipidomicsMicrobiotaAnimalsBacteriaFemaleGanglioside GalactosyltransferaseGlycolipidsKidneyLipid MetabolismMaleSex FactorsTranscriptomeGanglioside GalactosyltransferaseGlycolipidsUgt8a protein, mouse

Identifiers

PMID38609525
OpenAlexW4394753092

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.