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Study · Not a test of the peptide alone · 2009

5 results

Polymorphism in the oxytocin promoter region in patients with lactase non-persistence is not related to symptoms.

Truedsson M, Carlson J, Simrén M, Ohlsson B

BMC gastroenterology30 Nov 2009Cited by 5 (Europe PMC)

Summary

BackgroundOxytocin and the oxytocin receptor have been demonstrated in the gastrointestinal (GI) tract and have been shown to exert physiological effects on gut motility. The role for oxytocin in the pathophysiology of GI complaints is unknown. The aim of this study was to examine genetic variations or polymorphism of oxytocin (OXT) and its receptor (OXTR) genes in patients with GI complaints without visible organic abnormalities.MethodsGenetic variants in the OXT promoter region, and in the OXTR gene in DNA samples from 131 rigorously evaluated patients with Irritable Bowel Syndrome (IBS), 408 homozygous subjects referred for lactase (LCT-13910 C>T, rs4988235) genotyping, and 299 asymptomatic blood donors were compared. One polymorphism related to the OXT gene (rs6133010 A>G) and 4 related to the OXTR gene (rs1465386 G>T, rs3806675 G>A, rs968389 A>G, rs1042778 G>T) were selected for genotyping using Applied Biosystems 7900 HT allele discrimination assays.ResultsThere were no statistically significant differences in the genotype or allele frequencies in any of the SNPs when IBS patients were compared to healthy controls. Among subjects referred for lactase genotyping, the rs6133010 A>G OXT promoter A/G genotype tended to be more common in the 154 non-persistent (27.3%) subjects than in the 254 lactase persistant (18.1%) subjects and in the healthy controls (19.4%) (p = 0.08). When direct comparing, the A/G genotype was less common in the OXT promoter region in controls (p = 0.09) and in subjects with lactase persistence (p = 0.03) compared to subjects with lactase non-persistence. When healthy controls were viewed according to their own LCT-13910 genotypes, the C/C lactase non-persistent controls had a higher frequency for the OXT promoter A/G genotype than LCT-13910 T/T lactase persistent controls (41.2% vs 13.1%).No significant differences in frequencies of the investigated OXTR SNPs were noted in this study.ConclusionThe results suggest that polymorphism in the promoter region of the OXT gene is most common in subjects with lactase non-persistence. This polymorphism may not be related to GI symptoms, as it is related to lactase non-persistence also in healthy controls.
CC BYText from Europe PMC. Highlighted sentences are the source of results.

Results from this study5

No result from this study comes from a test of the peptide.

Studies that did not test the peptide alone5

In this study, Oxytocin was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking Oxytocin.

  1. 01HumanNot a test of Oxytocin aloneObservational studyOther

    In patients with irritable bowel syndrome, genotype and allele frequencies of the studied OXT and OXTR variants did not differ from healthy controls.

    In plain wordsIn people with irritable bowel syndrome, oxytocin gene variants were not more common than in healthy controls.

    Peptide
    Oxytocin
    Outcome
    No significant changeOXT and OXTR genotype and allele frequencies in IBS
    Study

    n: not reported in source

    Comparator
    Healthy controls
    Outcome group
    Genetic association · Gastrointestinal

    Source sentences

    Summary
    There were no statistically significant differences in the genotype or allele frequencies in any of the SNPs when IBS patients were compared to healthy controls.
    1 context sentence
    Summary · context
    Genetic variants in the OXT promoter region, and in the OXTR gene in DNA samples from 131 rigorously evaluated patients with Irritable Bowel Syndrome (IBS), 408 homozygous subjects referred for lactase (LCT-13910 C>T, rs4988235) genotyping, and 299 asymptomatic blood donors were compared.

    In this study, Oxytocin was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Oxytocin.

  2. 02HumanNot a test of Oxytocin aloneObservational studyOther

    The OXT promoter A/G genotype tended to be more common in lactase non-persistent subjects than in lactase persistent subjects and controls, not significantly.

    In plain wordsAn oxytocin gene variant tended to be more common in people with lactase non-persistence, but the difference was not significant.

    Peptide
    Oxytocin
    Outcome
    No significant changeOXT promoter A/G genotype in lactase non-persistence
    Study

    n: not reported in source

    Comparator
    Lactase persistent subjects and healthy controls
    Outcome group
    Genetic association · Gastrointestinal

    Measurements

    A/G genotype frequency
    27.3%
    lactase non-persistent
    A/G genotype frequency
    18.1%
    lactase persistent
    A/G genotype frequency
    19.4%
    healthy controls

    Source sentences

    Summary
    Among subjects referred for lactase genotyping, the rs6133010 A>G OXT promoter A/G genotype tended to be more common in the 154 non-persistent (27.3%) subjects than in the 254 lactase persistant (18.1%) subjects and in the healthy controls (19.4%) (p = 0.08).
    1 context sentence
    Summary · context
    Genetic variants in the OXT promoter region, and in the OXTR gene in DNA samples from 131 rigorously evaluated patients with Irritable Bowel Syndrome (IBS), 408 homozygous subjects referred for lactase (LCT-13910 C>T, rs4988235) genotyping, and 299 asymptomatic blood donors were compared.

    In this study, Oxytocin was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Oxytocin.

  3. 03HumanNot a test of Oxytocin aloneObservational studyOther

    The OXT promoter A/G genotype was less common in subjects with lactase persistence than in subjects with lactase non-persistence.

    In plain wordsAn oxytocin gene variant was less common in people with lactase persistence than in people with lactase non-persistence.

    Peptide
    Oxytocin
    Outcome
    Not applicableOXT promoter A/G genotype in lactase persistence versus non-persistence
    Study

    n: not reported in source

    Comparator
    Lactase non-persistent subjects
    Outcome group
    Genetic association · Gastrointestinal

    Source sentences

    Summary
    When direct comparing, the A/G genotype was less common in the OXT promoter region in controls (p = 0.09) and in subjects with lactase persistence (p = 0.03) compared to subjects with lactase non-persistence.
    1 context sentence
    Summary · context
    Genetic variants in the OXT promoter region, and in the OXTR gene in DNA samples from 131 rigorously evaluated patients with Irritable Bowel Syndrome (IBS), 408 homozygous subjects referred for lactase (LCT-13910 C>T, rs4988235) genotyping, and 299 asymptomatic blood donors were compared.

    In this study, Oxytocin was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Oxytocin.

  4. 04HumanNot a test of Oxytocin aloneObservational studyOther

    Among healthy controls, the OXT promoter A/G genotype was more frequent in C/C lactase non-persistent controls than in T/T lactase persistent controls.

    In plain wordsIn healthy people, an oxytocin gene variant was more common in those with lactase non-persistence genotypes than in those with persistence genotypes.

    Peptide
    Oxytocin
    Outcome
    Not applicableOXT promoter A/G genotype by LCT-13910 genotype in healthy controls
    Study

    n: not reported in source

    Comparator
    LCT-13910 T/T lactase persistent controls
    Outcome group
    Genetic association · Gastrointestinal

    Measurements

    A/G genotype frequency
    41.2%
    C/C lactase non-persistent controls
    A/G genotype frequency
    13.1%
    T/T lactase persistent controls

    Source sentences

    Summary
    When healthy controls were viewed according to their own LCT-13910 genotypes, the C/C lactase non-persistent controls had a higher frequency for the OXT promoter A/G genotype than LCT-13910 T/T lactase persistent controls (41.2% vs 13.1%)
    1 context sentence
    Summary · context
    Genetic variants in the OXT promoter region, and in the OXTR gene in DNA samples from 131 rigorously evaluated patients with Irritable Bowel Syndrome (IBS), 408 homozygous subjects referred for lactase (LCT-13910 C>T, rs4988235) genotyping, and 299 asymptomatic blood donors were compared.

    In this study, Oxytocin was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Oxytocin.

  5. 05HumanNot a test of Oxytocin aloneObservational studyOther

    No significant differences were noted in the frequencies of the investigated OXTR variants.

    In plain wordsNo significant differences were found in oxytocin receptor gene variants between the groups.

    Peptide
    Oxytocin
    Outcome
    No significant changeOXTR SNP frequencies
    Study

    n: not reported in source

    Outcome group
    Genetic association · Gastrointestinal

    Source sentences

    Summary
    No significant differences in frequencies of the investigated OXTR SNPs were noted in this study.
    1 context sentence
    Summary · context
    Genetic variants in the OXT promoter region, and in the OXTR gene in DNA samples from 131 rigorously evaluated patients with Irritable Bowel Syndrome (IBS), 408 homozygous subjects referred for lactase (LCT-13910 C>T, rs4988235) genotyping, and 299 asymptomatic blood donors were compared.

    In this study, Oxytocin was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Oxytocin.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    11 Oct 2026, 01:30 UTC

    Study results updated

  2. Version 1

    9 Oct 2026, 02:50 UTC

    First added · source update from Europe PMC

Subjects

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