Aberrant colon metabolome and the sudden infant death syndrome

被引:2
作者
Terry, Jefferson [1 ]
Dyer, Roger A. [2 ]
机构
[1] British Columbia Childrens & Womens Hosp, Dept Pathol, Vancouver, BC, Canada
[2] British Columbia Childrens Hosp, Res Inst, Analyt Core Metabol & Nutr, Vancouver, BC, Canada
关键词
SYNDROME SIDS; SEROTONIN; MICROBIOME; BACTERIA;
D O I
10.1038/s41390-023-02847-0
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: The Sudden Infant Death Syndrome (SIDS) has been associated with increased peripheral serotonin and an abnormal colonic microbiome, suggesting the colonic metabolome may also be abnormal. This study addresses this potential correlation by comparing colonic autopsy tissue from SIDS to age-matched non-SIDS controls.Methods: Untargeted metabolomic analysis by mass spectrometry is used to assess human colonic metabolomic differences including serotonin. Expression of genes associated with colonic serotonin synthesis and transport (TPH1, TPH2, DDC, SCL6A4) is measured by qRT-PCR. Microbiome analysis is performed to compare the SIDS and non-SIDS colonic microbiome.Results: Unsupervised hierarchical cluster and principal component analyses of metabolomic data shows increased variability in the SIDS cohort and separation of SIDS cases from the non-SIDS controls. There is a trend toward increased serotonin in the SIDS cohort but there is no significant difference in expression of the serotonin synthesis and transport genes between SIDS and non-SIDS control cohorts. Microbiome analysis shows no significant difference between the SIDS and non-SIDS control cohorts.Conclusions: This study demonstrates increased variability in the colonic metabolome and a trend towards increased colonic serotonin in SIDS. The underlying cause of colon metabolomic variability, and its potential role in SIDS pathogenesis, warrants further investigation.
引用
收藏
页码:634 / 640
页数:7
相关论文
共 25 条
  • [1] Enhancing diversity analysis by repeatedly rarefying next generation sequencing data describing microbial communities
    Cameron, Ellen S.
    Schmidt, Philip J.
    Tremblay, Benjamin J-M
    Emelko, Monica B.
    Muller, Kirsten M.
    [J]. SCIENTIFIC REPORTS, 2021, 11 (01)
  • [2] Maturation of the infant microbiome community structure and function across multiple body sites and in relation to mode of delivery
    Chu, Derrick M.
    Ma, Jun
    Prince, Amanda L.
    Antony, Kathleen M.
    Seferovic, Maxim D.
    Aagaard, Kjersti M.
    [J]. NATURE MEDICINE, 2017, 23 (03) : 314 - 326
  • [3] Statistical Methods for Handling Unwanted Variation in Metabolomics Data
    De Livera, Alysha M.
    Sysi-Aho, Marko
    Jacob, Laurent
    Gagnon-Bartsch, Johann A.
    Castillo, Sandra
    Simpson, Julie A.
    Speed, Terence P.
    [J]. ANALYTICAL CHEMISTRY, 2015, 87 (07) : 3606 - 3615
  • [4] The serotonin signaling system: From basic understanding to drug development-for functional GI disorders
    Gershon, Michael D.
    Tack, Jan
    [J]. GASTROENTEROLOGY, 2007, 132 (01) : 397 - 414
  • [5] Inconsistent classification of unexplained sudden deaths in infants and children hinders surveillance, prevention and research: recommendations from The 3rd International Congress on Sudden Infant and Child Death
    Goldstein, Richard D.
    Blair, Peter S.
    Sens, Mary Ann
    Shapiro-Mendoza, Carrie K.
    Krous, Henry F.
    Rognum, Torleiv O.
    Moon, Rachel Y.
    Anderson, Robert N.
    Bundock, Elizabeth A.
    Crandall, Laura G.
    Darnall, Robert A.
    Goldstein, Richard D.
    Hauck, Fern
    Haynes, Robin L.
    Himes, Barbara
    Hollander, Susan
    Holm, Ingrid A.
    Keywan, Christine
    McEntire, Betty
    Mitchell, Edwin A.
    Sperhake, Jan
    Sampson, Barbara A.
    Super, Mark
    [J]. FORENSIC SCIENCE MEDICINE AND PATHOLOGY, 2019, 15 (04) : 622 - 628
  • [6] High serum serotonin in sudden infant death syndrome
    Haynes, Robin L.
    Frelinger, Andrew L., III
    Giles, Emma K.
    Goldstein, Richard D.
    Tran, Hoa
    Kozakewich, Harry P.
    Haas, Elisabeth A.
    Gerrits, Anja J.
    Mena, Othon J.
    Trachtenberg, Felicia L.
    Paterson, David S.
    Berry, Gerard T.
    Adeli, Khosrow
    Kinney, Hannah C.
    Michelson, Alan D.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2017, 114 (29) : 7695 - 7700
  • [7] Gut microbiome in sudden infant death syndrome (SIDS) differs from that in healthy comparison babies and offers an explanation for the risk factor of prone position
    Highet, Amanda R.
    Berry, Anne M.
    Bettelheim, Karl A.
    Goldwater, Paul N.
    [J]. INTERNATIONAL JOURNAL OF MEDICAL MICROBIOLOGY, 2014, 304 (5-6) : 735 - 741
  • [8] Staphylococcal enterotoxin genes are common in Staphylococcus aureus intestinal flora in Sudden Infant Death Syndrome (SIDS) and live comparison infants
    Highet, Amanda R.
    Goldwater, Paul N.
    [J]. FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 2009, 57 (02): : 151 - 155
  • [9] Postmortem interval estimation: a novel approach utilizing gas chromatography/mass spectrometry-based biochemical profiling
    Kaszynski, Richard H.
    Nishiumi, Shin
    Azuma, Takeshi
    Yoshida, Masaru
    Kondo, Takeshi
    Takahashi, Motonori
    Asano, Migiwa
    Ueno, Yasuhiro
    [J]. ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2016, 408 (12) : 3103 - 3112
  • [10] The Serotonin Brainstem Hypothesis for the Sudden Infant Death Syndrome
    Kinney, Hannah C.
    Haynes, Robin L.
    [J]. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2019, 78 (09) : 765 - 779