Faecal short-chain fatty acids - a diagnostic biomarker for irritable bowel syndrome?

被引:83
作者
Farup, Per G. [1 ,2 ]
Rudi, Knut [3 ]
Hestad, Knut [1 ,4 ,5 ]
机构
[1] Innlandet Hosp Trust, Dept Res, N-2381 Brumunddal, Norway
[2] Norwegian Univ Sci & Technol, Unit Appl Clin Res, Dept Canc Res & Mol Med, Fac Med, N-7491 Trondheim, Norway
[3] Norwegian Univ Life Sci, Dept Chem Biotechnol & Food Sci, POB 5003, N-1432 As, Norway
[4] Norwegian Univ Sci & Technol, Fac Social Sci & Technol Management, Dept Psychol, N-7491 Trondheim, Norway
[5] Hedmark Univ Coll, Dept Publ Hlth, N-2418 Elverum, Norway
来源
BMC GASTROENTEROLOGY | 2016年 / 16卷
关键词
GUT MICROBIOTA; PREVALENCE; SYMPTOMS; BUTYRATE; HEALTH;
D O I
10.1186/s12876-016-0446-z
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: The diagnosis of irritable bowel syndrome (IBS) relies on symptom-based criteria. A valid and reliable biomarker that could confirm the diagnosis is desirable. This study evaluated the properties of faecal short-chain fatty acids (SCFA) as diagnostic biomarkers for IBS. Methods: Twenty-five subjects with IBS and 25 controls were included in this explanatory case-control study. Stool samples were analysed for SCFA (acetic acid, propionic acid, butyric acid, isobutyric acid, valeric acid, and isovaleric acid) with gas chromatography and reported as mmol/l and molar%. In the search for the best way to distinguish between subjects with and without IBS, the total amount and the amount of each of the SCFA were measured, and the proportions and differences between the SCFA were calculated. Results: In the IBS and control group, the mean age was 46.2 (SD 12.9) and 49.2 (SD 14.6), and the number of females was 13/25 (52 %) and 15/25 (60 %) respectively. The difference between propionic and butyric acid (mmol/l) had the best diagnostic properties, the area under the Receiver Operating Characteristic curve was 0.89 (95 % CI: 0.80-0.98) (p < 0.001). With a cut-off value > 0.015 mmol/l indicating IBS, the sensitivity, specificity, positive and negative likelihood ratio, and diagnostic odds ratio were 92 %, 72 %, 3.29, 0.11 and 29.6 respectively. Similar diagnostic properties were shown for all the IBS subgroups. Conclusions: The study indicated that faecal SCFA could be a non-invasive, valid and reliable biomarker for the differentiation of healthy subjects from subjects with IBS.
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页数:7
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共 36 条
  • [1] Ahmed IM, 2013, PLOS ONE, V8, DOI [10.1371/journal.pone.0077869, 10.1371/journal.pone.0058204]
  • [2] Is it who you are or what you do that is important in the human gut?
    Avershina, E.
    Rudi, K.
    [J]. BENEFICIAL MICROBES, 2013, 4 (03) : 219 - 222
  • [3] Cytokine imbalance in irritable bowel syndrome: a systematic review and meta-analysis
    Bashashati, M.
    Rezaei, N.
    Shafieyoun, A.
    McKernan, D. P.
    Chang, L.
    Oehman, L.
    Quigley, E. M.
    Schmulson, M.
    Sharkey, K. A.
    Simren, M.
    [J]. NEUROGASTROENTEROLOGY AND MOTILITY, 2014, 26 (07) : 1036 - 1048
  • [4] Cytokines and irritable bowel syndrome: Where do we stand?
    Bashashati, Mohammad
    Rezaei, Nima
    Andrews, Christopher N.
    Chen, Chun-Qiu
    Daryani, Nasser Ebrahimi
    Sharkey, Keith A.
    Storr, Martin A.
    [J]. CYTOKINE, 2012, 57 (02) : 201 - 209
  • [5] Beck AT., 1996, PsycTESTS, DOI DOI 10.1037/T00742-000
  • [6] Gut Microbiota as Potential Orchestrators of Irritable Bowel Syndrome
    Bennet, Sean M. P.
    Ohman, Lena
    Simren, Magnus
    [J]. GUT AND LIVER, 2015, 9 (03) : 318 - 331
  • [7] Rectal distention testing in patients with irritable bowel syndrome:: Sensitivity, specificity, and predictive values of pain sensory thresholds
    Bouin, M
    Plourde, V
    Boivin, M
    Riberdy, M
    Lupien, F
    Laganière, M
    Verrier, P
    Poitras, P
    [J]. GASTROENTEROLOGY, 2002, 122 (07) : 1771 - 1777
  • [8] Validating biomarkers of treatable mechanisms in irritable bowel syndrome
    Camilleri, M.
    Shin, A.
    Busciglio, I.
    Carlson, P.
    Acosta, A.
    Bharucha, A. E.
    Burton, D.
    Lamsam, J.
    Lueke, A.
    Donato, L. J.
    Zinsmeister, A. R.
    [J]. NEUROGASTROENTEROLOGY AND MOTILITY, 2014, 26 (12) : 1677 - 1685
  • [9] Irritable bowel syndrome: towards biomarker identification
    Clarke, Gerard
    Quigley, Eamonn M. M.
    Cryan, John F.
    Dinan, Timothy G.
    [J]. TRENDS IN MOLECULAR MEDICINE, 2009, 15 (10) : 478 - 489
  • [10] A methodological review of how heterogeneity has been examined in systematic reviews of diagnostic test accuracy
    Dinnes, J
    Deeks, J
    Kirby, J
    Roderick, P
    [J]. HEALTH TECHNOLOGY ASSESSMENT, 2005, 9 (12) : 1 - +