Transcriptome analysis suggests broad jejunal alterations in Linghu's obesity-diarrhea syndrome: A pilot study.

Xiao-Tong Niu, Xiang-Yao Wang, Yan Wang, Ke Han, Nan Ru, Jing-Yuan Xiang, En-Qiang Linghu
Author Information
  1. Xiao-Tong Niu: Medical School of Chinese PLA, Chinese PLA General Hospital, Beijing 100853, China.
  2. Xiang-Yao Wang: Department of Gastroenterology, The First Medical Center of Chinese PLA General Hospital, Beijing 100853, China.
  3. Yan Wang: Department of Gastroenterology, The First Medical Center of Chinese PLA General Hospital, Beijing 100853, China.
  4. Ke Han: Medical School of Chinese PLA, Chinese PLA General Hospital, Beijing 100853, China.
  5. Nan Ru: Department of Gastroenterology, The First Medical Center of Chinese PLA General Hospital, Beijing 100853, China.
  6. Jing-Yuan Xiang: Medical School of Chinese PLA, Chinese PLA General Hospital, Beijing 100853, China.
  7. En-Qiang Linghu: Department of Gastroenterology, The First Medical Center of Chinese PLA General Hospital, Beijing 100853, China. linghuenqiang@vip.sina.com.

Abstract

BACKGROUND: Obesity is associated with a significantly increased risk for chronic diarrhea, which has been proposed as Linghu's obesity-diarrhea syndrome (ODS); however, its molecular mechanisms are largely unknown.
AIM: To reveal the transcriptomic changes in the jejunum involved in ODS.
METHODS: In a cohort of 6 ODS patients (JOD group), 6 obese people without diarrhea (JO group), and 6 healthy controls (JC group), high-throughput sequencing and bioinformatics analyses were performed to identify jejunal mucosal mRNA expression alterations and dysfunctional biological processes. In another cohort of 16 ODS patients (SOD group), 16 obese people without diarrhea (SO group), and 16 healthy controls (SC group), serum diamine oxidase (DAO) and D-lactate (D-LA) concentrations were detected to assess changes in intestinal barrier function.
RESULTS: The gene expression profiles of jejunal mucosa in the JO and JC groups were similar, with only 1 differentially expressed gene (DEG). The gene expression profile of the JOD group was significantly changed, with 411 DEGs compared with the JO group and 211 DEGs compared with the JC group, 129 of which overlapped. The enrichment analysis of these DEGs showed that the biological processes such as digestion, absorption, and transport of nutrients (especially lipids) tended to be up-regulated in the JOD group, while the biological processes such as rRNA processing, mitochondrial translation, antimicrobial humoral response, DNA replication, and DNA repair tended to be down-regulated in the JOD group. Eight DEGs (, , , , , , , and ) may play a key regulatory role in the pathological process of ODS, and their expression levels were significantly decreased in ODS patients ( < 0.001). In the second cohort, compared with healthy controls, the levels of serum intestinal barrier function markers (DAO and D-LA) were significantly increased in all obese individuals ( < 0.01), but were higher in the SOD group than in the SO group ( < 0.001).
CONCLUSION: Compared with healthy controls and obese individuals without diarrhea, patients with Linghu's ODS had extensive transcriptomic changes in the jejunal mucosa, likely affecting intestinal barrier function and thus contributing to the obesity and chronic diarrhea phenotypes.

Keywords

References

  1. Int J Mol Sci. 2018 Oct 25;19(11): [PMID: 30366466]
  2. Best Pract Res Clin Endocrinol Metab. 2012 Dec;26(6):791-804 [PMID: 23168280]
  3. Metabolism. 2022 Aug;133:155217 [PMID: 35584732]
  4. Cells. 2020 Jul 10;9(7): [PMID: 32664329]
  5. Biochimie. 2016 May;124:11-20 [PMID: 26133659]
  6. Proc Natl Acad Sci U S A. 2005 Oct 25;102(43):15545-50 [PMID: 16199517]
  7. Metabolism. 2024 Jan;150:155712 [PMID: 37884078]
  8. Chin Med J (Engl). 2022 Aug 05;135(15):1806-1807 [PMID: 35512792]
  9. Int J Mol Sci. 2022 Apr 01;23(7): [PMID: 35409299]
  10. Dig Dis Sci. 2020 May;65(5):1414-1422 [PMID: 31605277]
  11. J Gastroenterol Hepatol. 2017 Jan;32(1):53-63 [PMID: 27087165]
  12. Gut. 2018 Aug;67(8):1380-1399 [PMID: 29653941]
  13. Nutrients. 2019 Mar 01;11(3): [PMID: 30832230]
  14. Clin Mol Hepatol. 2021 Jan;27(1):157-174 [PMID: 33238333]
  15. Gut. 2013 Jun;62(6):933-47 [PMID: 23481261]
  16. Cell Metab. 2015 Jul 7;22(1):113-24 [PMID: 26094890]
  17. J Pathol. 2018 Oct;246(2):217-230 [PMID: 29984492]
  18. Cell Host Microbe. 2018 Apr 11;23(4):458-469.e5 [PMID: 29649441]
  19. Mol Carcinog. 2019 Sep;58(9):1531-1550 [PMID: 31168912]
  20. Int J Mol Sci. 2019 Mar 06;20(5): [PMID: 30845725]
  21. Nature. 2016 Oct 13;538(7624):260-264 [PMID: 27698416]
  22. Cell Microbiol. 2015 Nov;17(11):1561-9 [PMID: 26294173]
  23. Sci Rep. 2023 Jul 7;13(1):11038 [PMID: 37419941]
  24. Genome Biol. 2014;15(12):550 [PMID: 25516281]
  25. Animals (Basel). 2023 Sep 14;13(18): [PMID: 37760316]
  26. Ann Intern Med. 2024 May;177(5):ITC65-ITC80 [PMID: 38739920]
  27. Obes Rev. 2020 Feb;21(2):e12958 [PMID: 31777187]
  28. Cell Rep. 2023 Feb 28;42(2):112084 [PMID: 36753416]
  29. Am J Gastroenterol. 2004 Sep;99(9):1801-6 [PMID: 15330922]
  30. Mol Cell. 2023 Jan 5;83(1):26-42.e13 [PMID: 36608667]
  31. Metab Syndr Relat Disord. 2015 Dec;13(10):423-44 [PMID: 26569333]
  32. Mutat Res Rev Mutat Res. 2018 Oct - Dec;778:23-37 [PMID: 30454680]
  33. Aliment Pharmacol Ther. 2019 Nov;50(9):1019-1024 [PMID: 31532005]
  34. Genes Dis. 2018 Mar 10;5(4):367-373 [PMID: 30591939]
  35. Biol Trace Elem Res. 2020 Oct;197(2):384-393 [PMID: 31902098]
  36. BMC Bioinformatics. 2011 Aug 04;12:323 [PMID: 21816040]
  37. Nat Rev Microbiol. 2021 Jan;19(1):55-71 [PMID: 32887946]
  38. Biochimie. 2013 Mar;95(3):585-94 [PMID: 23274128]
  39. Commun Biol. 2020 May 22;3(1):257 [PMID: 32444826]
  40. Pathol Oncol Res. 2020 Apr;26(2):635-639 [PMID: 31165996]
  41. BMC Bioinformatics. 2008 Dec 29;9:559 [PMID: 19114008]
  42. EMBO Rep. 2020 Jul 3;21(7):e50047 [PMID: 32567155]
  43. Semin Cancer Biol. 2023 Jul;92:16-27 [PMID: 36965839]
  44. Nutr Clin Pract. 2012 Apr;27(2):201-14 [PMID: 22367888]
  45. Nutr Diabetes. 2018 Sep 24;8(1):53 [PMID: 30250193]
  46. Gut. 2021 Jun;70(6):1098-1109 [PMID: 32994312]
  47. J Clin Oncol. 2016 Dec 10;34(35):4225-4230 [PMID: 27903150]
  48. Science. 2021 Aug 13;373(6556):813-818 [PMID: 34385401]
  49. J Physiol Biochem. 2006 Dec;62(4):303-6 [PMID: 17615956]
  50. Cell Mol Life Sci. 2011 Jul;68(13):2215-29 [PMID: 21560070]
  51. Cell Metab. 2014 Dec 2;20(6):967-77 [PMID: 25456739]
  52. Mol Metab. 2022 Sep;63:101546 [PMID: 35817394]
  53. Curr Oncol Rep. 2019 Mar 27;21(5):41 [PMID: 30919143]
  54. J Pathol. 2023 Mar;259(3):233-235 [PMID: 36541916]
  55. Mol Med Rep. 2012 Apr;5(4):1027-32 [PMID: 22246134]
  56. Eur J Clin Nutr. 2014 Nov;68(11):1264-6 [PMID: 25226827]

MeSH Term

Humans
Jejunum
Male
Pilot Projects
Female
Diarrhea
Adult
Intestinal Mucosa
Obesity
Middle Aged
Gene Expression Profiling
Transcriptome
Case-Control Studies
Syndrome
Amine Oxidase (Copper-Containing)
Computational Biology
Lactic Acid
Chronic Disease

Chemicals

Amine Oxidase (Copper-Containing)
Lactic Acid

Word Cloud

Created with Highcharts 10.0.0groupODSdiarrheasignificantlypatientsJODobesehealthycontrolsjejunalexpressionbarrierDEGsLinghu'schangescohort6withoutJOJCbiologicalprocesses16intestinalfunctiongenecompared<0Obesityincreasedchronicobesity-diarrheatranscriptomicpeoplealterationsSODSOserumDAOD-LAmucosaanalysistendedDNAlevels001individualsTranscriptomeBACKGROUND:associatedriskproposedsyndromehowevermolecularmechanismslargelyunknownAIM:revealjejunuminvolvedMETHODS:high-throughputsequencingbioinformaticsanalysesperformedidentifymucosalmRNAdysfunctionalanotherSCdiamineoxidaseD-lactateconcentrationsdetectedassessRESULTS:profilesgroupssimilar1differentiallyexpressedDEGprofilechanged411211129overlappedenrichmentshoweddigestionabsorptiontransportnutrientsespeciallylipidsup-regulatedrRNAprocessingmitochondrialtranslationantimicrobialhumoralresponsereplicationrepairdown-regulatedEightmayplaykeyregulatoryrolepathologicalprocessdecreasedsecondmarkers01higherCONCLUSION:Comparedextensivelikelyaffectingthuscontributingobesityphenotypessuggestsbroadsyndrome:pilotstudyChronicIntestinalJejunum

Similar Articles

Cited By