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Assessing the Drug Exposure Risk of Infants Breastfed by Women With Inflammatory Bowel Disease

Assessing the Drug Exposure Risk of Infants Breastfed by Women With Inflammatory Bowel Disease

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03397108
Enrollment
79
Registered
2018-01-11
Start date
2017-08-31
Completion date
2024-11-05
Last updated
2025-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Crohn's Disease, Healthy Controls, Ulcerative Colitis

Keywords

Inflammatory Bowel Disease, Crohn disease, Colitis, TNF, Breast milk, monoclonal antibody

Brief summary

Breastfeeding is beneficial to both mother and baby. However, many breastfeeding women are affected by long-term health conditions and need to take medications. Inflammatory Bowel Disease (IBD) is marked by an abnormal response of the body's immune system, and high levels of certain proteins that cause inflammation (Cytokines like Tumor Necrosis Factor-alpha or TNF). A group of drugs called biologics target and stop these proteins from causing inflammation, and have been successfully used to treat this condition. Inflammatory proteins may be present in breast milk of healthy women in variable levels, and may play a role in development of infant's brain and immune system. This observational study is conducted to investigate: * Concentration of some of the inflammatory proteins in breast milk of mothers with IBD and healthy controls * Interaction between these proteins and biologics in breast milk of women with IBD * Potential role of these proteins (and their interaction with biologics) on development of infant learning and memory function It has been presumed that concentrations of TNF and some other cytokines are higher in breast milk of women with IBD, and the biologics can normalize these high levels. Note: Due to the pandemic, the study now consists of reduced number of study visits. The mandatory visits include two home visits in the first 4 months postpartum to complete a participant questionnaire and collect a small sample of breast milk at each visit. The optional study visits consist of two visits at the Hospital for Sick Children for evaluation of learning and memory function of the infant at the ages of 12 and 18 months. Additionally, mothers will be required to complete for their infant subscales of The Ages and Stages Questionnaires®, Third Edition (ASQ®-3) either in person or over the telephone at the ages of 12 months and 18 months.

Detailed description

The inflammatory bowel disease (IBD) shows the highest incidence among people of childbearing age. Indeed, it is not uncommon that pregnant or lactating women with IBD require drug therapy, including monoclonal antibodies against Tumor Necrosis Factor-alpha (TNF). TNF and TNF-dependent chemokines are normally expressed in milk. Importantly, experimental data indicate enhanced brain growth and cognitive development in the mouse offspring given milk deficient in TNF and TNF-dependent chemokines. Patients with IBD are often treated with monoclonal antibodies against TNF (TNFmAb). Although TNFmAb is used during breastfeeding due to their minimal milk excretion, whether it affects endogenous TNF/chemokines in human milk is not known. Our hypotheses are: 1) Women with IBD have higher TNF (and TNF-dependent chemokines) in milk than non-IBD control women, because of the inflammatory condition; and 2) Women with IBD receiving TNFmAb have lower TNF (and TNF-dependent chemokines) in milk than those with IBD who are not treated with TNFmAb. We conduct an observational study of breastfeeding women with or without IBD. Some of these women with IBD are likely to be receiving TNFmAb. We measure milk concentrations of TNF and TNF-dependent chemokines in early (5-6 weeks postpartum) and mid-lactation period (13-14 weeks postpartum). Also, as an exploratory analysis, we assess their infant's cognitive and language development at 12 month and 18 months using Bayley-III tool. Note: Because there was no information at the outset of the study on cytokine profiles in milk of women with inflammatory conditions including IBD, a formal sample size could not be estimated. Although a provisional target was set, the study was designed to continue for the planned study duration as no stopping rule had been defined. Also, our original protocol included a population pharmacokinetic study of TNFmAb in milk. However, due to the pandemic and difficulty in developing the assay method, we were not able to start this part of the project.

Interventions

OTHERThe IBD group was divided into 2 subgroups: with or without anti-TNF antibody use

This observational study enrolled women with IBD, and some of them were receiving a treatment with anti-TNF monoclonal antibody, which was prescribed by their responsible prescribers at a standard dose and dosing interval.

Sponsors

MOUNT SINAI HOSPITAL
CollaboratorOTHER
Crohn's and Colitis Foundation
CollaboratorOTHER
The Hospital for Sick Children
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Breastfeeding women with IBD or healthy breastfeeding women in the first 4-month postpartum period

Exclusion criteria

* unable to communicate in English * Present illness of chronic inflammatory conditions (except IBD) * Mastitis * Present acute or chronic infection * use of a different anti-Tumor Necrosis Factor (TNF) drug within the last 2 months

Design outcomes

Primary

MeasureTime frameDescription
Levels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayTwo points at early-lactation (median 5-6 postpartum weeks) and mid-lactation (median 13-14 postpartum weeks)This observational study collected milk samples during the defined study periods: early-lactation and mid-lactation. To capture a temporal profiles of Tumour Necrosis Factor (TNF) and TNF-dependent chemokine levels, we analyzed these 2 sampling periods separately, instead of pooling them per sampling period. Multiplex assay was used to measure TNF and TNF-dependent downstream chemokines including MCP-1 (CCL2), MIP-1beta (CCL4) and IP10 (CXCL10) in breast milk of two groups of participants (women with IBD and healthy controls) at two sampling periods (early- and mid-lactation). Our original plan included MCP-3 (CCL7) as well, but an average quantification rate for this chemokine was only 33%, and therefore we excluded MCP-3 from our analyses.

Secondary

MeasureTime frameDescription
Scores on Cognitive Subset of Bayley Scales of Infant and Toddler Development- Third Version (Bayley-III) in Infants of Healthy Controls and Women With IBDAt the infant age of 12 months and 18 monthsWe used Bayley Scales of Infant and Toddler development- Third Version (Bayley-III): which is used widely to measure child's cognitive and language development. In this scale, for both cognitive and language scores, minimum standard score is 45 and maximum standard score is 155: Higher standard scores indicates stronger/better performance. Children of the participating mothers were tested at the age of 12 months and 18 months. The language assessment is also used for comprehensiveness, but this has been added after the study was started. The test is performed as a single-blinded assessment in a controlled environment at the Hospital for Sick Children by a trained psychometrist supervised by a psychologist.

Other

MeasureTime frameDescription
Population Pharmacokinetic Study of Anti-TNF Monoclonal Antibody in Milk1-2 monthsConcentrations of anti-TNF monoclonal antibody in milk will be measured once the method is validated. The data will be analyzed using population pharmacokinetic modeling.
Milk Sampling Time Point in the Early Lactation Periodpostpartum weeks until 10 weeks.This is the early lactation sampling points: one of the two milk sampling time points (post-partum weeks). The milk samples were analyzed for their TNF and chemokine levels.
Milk Sampling Time Point in the Mid Lactation Periodpostpartum weeks of 10-20 weeks.This is the second milk sampling point corresponding to the mid-lactation period.

Countries

Canada

Participant flow

Recruitment details

Participants enrolled between August 2017 to November 2022

Participants by arm

ArmCount
Women With IBD
This group is composed of breastfeeding women aged over 18 years and in their first 4-month postpartum period, who are diagnosed with Crohn's disease or Ulcerative Colitis.
26
Healthy Breastfeeding Women
This group is composed of healthy breastfeeding women aged over 18 years and in their first 4-month postpartum period.
31
Total57

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyInsufficient milk production32
Overall StudyLost to Follow-up150
Overall StudyWithdrawal by Subject20

Baseline characteristics

CharacteristicTotalWomen With IBDHealthy Breastfeeding Women
Age, Continuous34 years34 years34 years
Breastfeeding status
Exclusive breastfeeding
39 participants16 participants23 participants
Breastfeeding status
Predominant (>80% of time)
14 participants8 participants6 participants
Breastfeeding status
Usual (<80% of time)
4 participants2 participants2 participants
Infant birth weight3376.5 grams3351 grams3402 grams
Infant Sex: Female28 participants15 participants13 participants
Maternal BMI24.5 kg/m^225 kg/m^224 kg/m^2
Maternal Weight67 kg68 kg66 kg
Mode of Delivery
C-section
14 participants10 participants4 participants
Mode of Delivery
Vaginal
43 participants16 participants27 participants
Pregnancy period39 week39 week39 week
Race and Ethnicity Not Collected0 Participants
Region of Enrollment
Canada
57 participants26 participants31 participants
Sex/Gender, Customized
Female
57 participants26 participants31 participants
Smoking during pregnancy0 participants0 participants0 participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 460 / 33
other
Total, other adverse events
0 / 460 / 33
serious
Total, serious adverse events
0 / 460 / 33

Outcome results

Primary

Levels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex Assay

This observational study collected milk samples during the defined study periods: early-lactation and mid-lactation. To capture a temporal profiles of Tumour Necrosis Factor (TNF) and TNF-dependent chemokine levels, we analyzed these 2 sampling periods separately, instead of pooling them per sampling period. Multiplex assay was used to measure TNF and TNF-dependent downstream chemokines including MCP-1 (CCL2), MIP-1beta (CCL4) and IP10 (CXCL10) in breast milk of two groups of participants (women with IBD and healthy controls) at two sampling periods (early- and mid-lactation). Our original plan included MCP-3 (CCL7) as well, but an average quantification rate for this chemokine was only 33%, and therefore we excluded MCP-3 from our analyses.

Time frame: Two points at early-lactation (median 5-6 postpartum weeks) and mid-lactation (median 13-14 postpartum weeks)

Population: Control is non-IBD breastfeeding women. IBD group was divided into 2 subgroups based on the status of their treatment with anti-TNF antibody (TNFmAb). Participants were tested twice: first, during early lactation period and second, later during mid-lactation period. Six women in IBD group could not provide milk samples during the mid-lactation period. MCP-3 (CCL7) detection rate was 33% of all samples and therefore excluded from the analyses.

ArmMeasureGroupValue (MEDIAN)
Healthy Breastfeeding WomenLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation: TNF12.5 pg/ml
Healthy Breastfeeding WomenLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation: MCP11078.0 pg/ml
Healthy Breastfeeding WomenLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation:MIP1beta13.4 pg/ml
Healthy Breastfeeding WomenLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation: IP103985.0 pg/ml
Healthy Breastfeeding WomenLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation: TNF11.1 pg/ml
Healthy Breastfeeding WomenLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation: MCP1513.1 pg/ml
Healthy Breastfeeding WomenLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation: MIP1beta8.2 pg/ml
Healthy Breastfeeding WomenLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation: IP102041.0 pg/ml
Healthy Breastfeeding WomenLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation MCP-3NA pg/ml
Healthy Breastfeeding WomenLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation MCP-3NA pg/ml
Women With IBDLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation:MIP1beta12.6 pg/ml
Women With IBDLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation MCP-3NA pg/ml
Women With IBDLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation: IP102302.0 pg/ml
Women With IBDLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation: TNF16.4 pg/ml
Women With IBDLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation: MCP1679.5 pg/ml
Women With IBDLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation: MIP1beta16.4 pg/ml
Women With IBDLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation MCP-3NA pg/ml
Women With IBDLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation: IP101277.0 pg/ml
Women With IBDLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation: TNF19.8 pg/ml
Women With IBDLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation: MCP11325.0 pg/ml
IBD Subgroup On TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation: IP10981.9 pg/ml
IBD Subgroup On TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation: MIP1beta6.9 pg/ml
IBD Subgroup On TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation MCP-3NA pg/ml
IBD Subgroup On TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation: TNF7.1 pg/ml
IBD Subgroup On TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation: IP10898.8 pg/ml
IBD Subgroup On TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation: MCP1305.8 pg/ml
IBD Subgroup On TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation MCP-3NA pg/ml
IBD Subgroup On TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation: MCP1339.6 pg/ml
IBD Subgroup On TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation: TNF7.3 pg/ml
IBD Subgroup On TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation:MIP1beta7.1 pg/ml
IBD Subgroup Off TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation: TNF18.8 pg/ml
IBD Subgroup Off TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation: IP101820.0 pg/ml
IBD Subgroup Off TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation: MCP1693.8 pg/ml
IBD Subgroup Off TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation MCP-3NA pg/ml
IBD Subgroup Off TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayMid-lactation: MIP1beta18.1 pg/ml
IBD Subgroup Off TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation: MCP11352.0 pg/ml
IBD Subgroup Off TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation:MIP1beta17.7 pg/ml
IBD Subgroup Off TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation: IP103360.0 pg/ml
IBD Subgroup Off TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation: TNF23.5 pg/ml
IBD Subgroup Off TNFmAb TreatmentLevels of TNF (Tumor Necrosis Factor Alpha) and TNF-dependent Chemokines (MCP1, MIP-1beta and IP10) in Breast Milk of Women With IBD and Healthy Controls by Multiplex AssayEarly-lactation MCP-3NA pg/ml
Comparison: Milk TNF levels at EARLY LACTATION PERIOD were compared between non-IBD control and women with IBD. Our hypothesis was that women with IBD have higher TNF in milk due to the underlying inflammatory condition (IBD).p-value: 0.89Wilcoxon (Mann-Whitney)
Comparison: Milk TNF at the EARLY LACTATION PERIOD was compared among the 3 groups: non-IBD control, IBD subgroup On TNFmAb and IBD subgroup Off TNFmAb. We hypothesized that the use of TNFmAb decreases milk TNF. Nonparametric comparison of 3 groups was done with one-way ANOVA on ranks (Kruskal-Wallis test), followed by multiplicity-adjusted pairwise comparisons with Dunn's test.p-value: 0.024Kruskal-Wallis
Comparison: Milk MCP1 levels (TNF dependent chemokine) at the EARLY LACTATION PERIOD were compared between non-IBD control and IBD group to see if there is a difference.p-value: 0.7Wilcoxon (Mann-Whitney)
Comparison: Milk levels of MIP-1 beta (TNF dependent chemokine) at the EARLY LACTATION PERIOD were compared between non-IBD control and IBD group to see if there is a difference.p-value: 0.93Wilcoxon (Mann-Whitney)
Comparison: Milk IP10 levels (one of the TNF dependent chemokines) at EARLY LACTATION PERIOD were compared between non-IBD control and IBD group to see if there is a difference.p-value: 0.12Wilcoxon (Mann-Whitney)
Comparison: Milk levels of TNF-dependent chemokine, MCP1, at the EARLY LACTATION PERIOD was compared among the 3 groups: non-IBD control and the 2 IBD subgroups. We hypothesized that the use of TNFmAb decreases milk TNF and TNF-dependent chemokine including MCP1. Nonparametric comparison of the 3 groups was done with one-way ANOVA on ranks (Kruskal-Wallis test), followed by multiplicity-adjusted pairwise comparisons with Dunn's test.p-value: 0.12Kruskal-Wallis
Comparison: Milk MIP-1beta at the EARLY LACTATION PERIOD was compared among the 3 groups: non-IBD control, IBD subgroup On TNFmAb and IBD subgroup Off TNFmAb. We hypothesized that the use of TNFmAb decreases milk TNF and TNF-dependent chemokine including MIP-1beta. Nonparametric comparison of 3 groups was done with one-way ANOVA on ranks (Kruskal-Wallis test), followed by multiplicity-adjusted pairwise comparisons with Dunn's test.p-value: 0.051Kruskal-Wallis
Comparison: Milk IP10 at the EARLY LACTATION PERIOD was compared among the 3 groups: non-IBD control, IBD subgroup On TNFmAb and IBD subgroup Off TNFmAb. We hypothesized that the use of TNFmAb decreases milk TNF and TNF-dependent chemokine including IP10. Nonparametric comparison of 3 groups was done with one-way ANOVA on ranks (Kruskal-Wallis test), followed by multiplicity-adjusted pairwise comparisons with Dunn's test.p-value: 0.0046Kruskal-Wallis
Comparison: Comparison of milk TNF level at the MID LACTATION POINT between non-IBD control and IBD group. The same analytical framework as the early lactation, but this is based on data at the mid-lactation point (13-14 postpartum weeks). Our hypothesis is the same as for the early-lactation point.p-value: 0.35Wilcoxon (Mann-Whitney)
Comparison: Milk TNF at MID LACTATION POINT was compared among the 3 groups: non-IBD control, IBD subgroup On TNFmAb and IBD subgroup Off TNFmAb. Hypothesis is the same as for the early lactation point. Nonparametric comparison of 3 groups was done with one-way ANOVA on ranks (Kruskal-Wallis test), followed by multiplicity-adjusted pairwise comparisons with Dunn's test.p-value: 0.11Kruskal-Wallis
Comparison: Milk MCP1 level comparison between non-IBD control and IBD group at the MID LACTATION POINT(13-14 postpartum weeks). Our hypothesis is the same as for the early-lactation point.p-value: 0.26Wilcoxon (Mann-Whitney)
Comparison: Milk MIP-1beta level comparison between non-IBD control and IBD group at the MID LACTATION POINT (13-14 postpartum weeks). Our hypothesis is the same as for the early-lactation point.p-value: 0.15Wilcoxon (Mann-Whitney)
Comparison: Milk IP10 level comparison between non-IBD control and IBD group at the MID LACTATION POINT (13-14 postpartum weeks). Our hypothesis is the same as for the early-lactation point.p-value: 0.31Wilcoxon (Mann-Whitney)
Comparison: Milk MCP-1 at the MID LACTATION PERIOD was compared among the 3 groups: non-IBD control, IBD subgroup On TNFmAb and IBD subgroup Off TNFmAb. The hypothesis is the same as that for the early-lactation period. Nonparametric comparison of 3 groups was done with one-way ANOVA on ranks (Kruskal-Wallis test), followed by multiplicity-adjusted pairwise comparisons with Dunn's test.p-value: 0.21Kruskal-Wallis
Comparison: Milk MIP-1beta at the MID LACTATION POINT was compared among the 3 groups: non-IBD control, IBD subgroup On TNFmAb and IBD subgroup Off TNFmAb. The hypothesis is the same as that for the early-lactation period. Nonparametric comparison of 3 groups was done with one-way ANOVA on ranks (Kruskal-Wallis test), followed by multiplicity-adjusted pairwise comparisons with Dunn's test.p-value: 0.12Kruskal-Wallis
Comparison: Milk IP10 at the MID LACTATION POINT was compared among the 3 groups: non-IBD control, IBD subgroup On TNFmAb and IBD subgroup Off TNFmAb. The same hypothesis as that for the early-lactation period. Nonparametric comparison of 3 groups was done with one-way ANOVA on ranks (Kruskal-Wallis test), followed by multiplicity-adjusted pairwise comparisons with Dunn's test.p-value: 0.29Kruskal-Wallis
Comparison: Using the pooled data of all participants at the EARLY LACTATION, we analyzed correlation between milk TNF and chemokine MCP1 to see if they are positively correlated. This is to show supportive evidence for TNF dependency of chemokine MCP1.p-value: <0.000195% CI: [0.5647, 0.8303]Spearman rank correlation
Comparison: Using the pooled data of all participants at the EARLY LACTATION, we analyzed correlation between milk TNF and chemokine MIP-1beta to see if they are positively correlated. This is to show supportive evidence for TNF dependency of chemokine MIP-1beta.p-value: <0.000195% CI: [0.5088, 0.8042]Spearman rank correlation
Comparison: Using the pooled data of all participants at the EARLY LACTATION, we analyzed correlation between milk TNF and chemokine IP10 to see if they are positively correlated. This is to show supportive evidence for TNF dependency of chemokine IP10.p-value: <0.000195% CI: [0.4377, 0.7693]Spearman rank correlation
Comparison: Using the pooled data of all participants at the MID LACTATION POINT, we analyzed correlation between milk TNF and MCP1 to see of they are positively correlated.p-value: <0.000195% CI: [0.3445, 0.736]Spearman rank correlation
Comparison: Using the pooled data of all participants at the MID LACTATION POINT, we analyzed correlation between milk TNF and MIP-1beta to see of they are positively correlated.p-value: <0.000195% CI: [0.6022, 0.8562]Spearman rank correlation
Comparison: Using the pooled data of all participants at the MID LACTATION POINT, we analyzed correlation between milk TNF and IP10 to see of they are positively correlated.p-value: 0.022795% CI: [0.03869, 0.552]Spearman rank correlation
Comparison: Using the pooled data of all participants, we assessed temporal tracking of milk TNF between early and mid-lactation points.p-value: 0.000195% CI: [0.2727, 0.6975]Spearman rank correlation
Comparison: Using the pooled data of all participants, we assessed temporal tracking of milk MCP1 between early and mid-lactation points.p-value: 0.000595% CI: [0.2181, 0.6664]Spearman rank correlation
Comparison: Using the pooled data of all participants, we assessed temporal tracking of milk MIP-1beta between early and mid-lactation points.p-value: 0.0195% CI: [0.0802, 0.5803]Spearman rank correlation
Comparison: Using the pooled data of all participants, we assessed temporal tracking of milk IP10 between early and mid-lactation points.p-value: <0.000195% CI: [0.467, 0.7964]Spearman rank correlation
Secondary

Scores on Cognitive Subset of Bayley Scales of Infant and Toddler Development- Third Version (Bayley-III) in Infants of Healthy Controls and Women With IBD

We used Bayley Scales of Infant and Toddler development- Third Version (Bayley-III): which is used widely to measure child's cognitive and language development. In this scale, for both cognitive and language scores, minimum standard score is 45 and maximum standard score is 155: Higher standard scores indicates stronger/better performance. Children of the participating mothers were tested at the age of 12 months and 18 months. The language assessment is also used for comprehensiveness, but this has been added after the study was started. The test is performed as a single-blinded assessment in a controlled environment at the Hospital for Sick Children by a trained psychometrist supervised by a psychologist.

Time frame: At the infant age of 12 months and 18 months

Population: Language test was introduced to the project for completeness after the study had started. This created lower sample numbers at the 12 month point.

ArmMeasureGroupValue (MEAN)Dispersion
Healthy Breastfeeding WomenScores on Cognitive Subset of Bayley Scales of Infant and Toddler Development- Third Version (Bayley-III) in Infants of Healthy Controls and Women With IBDCognitive at 12 month103.0 score on a scaleStandard Deviation 7
Healthy Breastfeeding WomenScores on Cognitive Subset of Bayley Scales of Infant and Toddler Development- Third Version (Bayley-III) in Infants of Healthy Controls and Women With IBDLanguage at 12 month105.4 score on a scaleStandard Deviation 9.7
Healthy Breastfeeding WomenScores on Cognitive Subset of Bayley Scales of Infant and Toddler Development- Third Version (Bayley-III) in Infants of Healthy Controls and Women With IBDCognitive at 18 month108.8 score on a scaleStandard Deviation 8.6
Healthy Breastfeeding WomenScores on Cognitive Subset of Bayley Scales of Infant and Toddler Development- Third Version (Bayley-III) in Infants of Healthy Controls and Women With IBDLanguage at 18 month107.0 score on a scaleStandard Deviation 15.6
Women With IBDScores on Cognitive Subset of Bayley Scales of Infant and Toddler Development- Third Version (Bayley-III) in Infants of Healthy Controls and Women With IBDLanguage at 18 month105.3 score on a scaleStandard Deviation 13
Women With IBDScores on Cognitive Subset of Bayley Scales of Infant and Toddler Development- Third Version (Bayley-III) in Infants of Healthy Controls and Women With IBDCognitive at 12 month107.1 score on a scaleStandard Deviation 8.8
Women With IBDScores on Cognitive Subset of Bayley Scales of Infant and Toddler Development- Third Version (Bayley-III) in Infants of Healthy Controls and Women With IBDCognitive at 18 month114.7 score on a scaleStandard Deviation 10.8
Women With IBDScores on Cognitive Subset of Bayley Scales of Infant and Toddler Development- Third Version (Bayley-III) in Infants of Healthy Controls and Women With IBDLanguage at 12 month107.7 score on a scaleStandard Deviation 8.3
Comparison: Cognitive development at 12 months of age. Animal data suggested that pups receiving milk with lower TNF and TNF-dependent chemokines showed enhanced cognitive development. Because there was no guiding information in humans regarding milk TNF level differences between women with and without IBD, our main goal was to measure milk TNF levels. The infant cognitive/language assessment, therefore, had to be designed as a pilot and exploratory in nature.p-value: 0.12t-test, 2 sided
Comparison: Language development at 12 months of age.p-value: 0.56t-test, 2 sided
Comparison: Cognitive development at 18 months of age.p-value: 0.16t-test, 2 sided
Comparison: Language development at 18 months of agep-value: 0.75t-test, 2 sided
Comparison: Using pooled data of all participants at the early-lactation sample point, correlation between milk TNF levels and 12 month cognitive development was examined to investigate if they were inversely correlated.p-value: 0.085395% CI: [-0.047, 0.5307]Spearman rank correlation
Comparison: Using the pooled data of all participants, correlation analysis between milk TNF at early lactation and 12 month language score was done to see if they were inversely correlated.p-value: 0.0995% CI: [-0.07385, 0.6921]Spearman rank correlation
Other Pre-specified

Milk Sampling Time Point in the Early Lactation Period

This is the early lactation sampling points: one of the two milk sampling time points (post-partum weeks). The milk samples were analyzed for their TNF and chemokine levels.

Time frame: postpartum weeks until 10 weeks.

ArmMeasureValue (MEDIAN)
Healthy Breastfeeding WomenMilk Sampling Time Point in the Early Lactation Period5.3 postpartum weeks
Women With IBDMilk Sampling Time Point in the Early Lactation Period5.5 postpartum weeks
IBD Subgroup On TNFmAb TreatmentMilk Sampling Time Point in the Early Lactation Period6.0 postpartum weeks
IBD Subgroup Off TNFmAb TreatmentMilk Sampling Time Point in the Early Lactation Period5.4 postpartum weeks
Comparison: This is to confirm that the 2 groups are not different for their sampling time points in the early lactation period.p-value: 0.97Wilcoxon (Mann-Whitney)
p-value: 0.96Kruskal-Wallis
Other Pre-specified

Milk Sampling Time Point in the Mid Lactation Period

This is the second milk sampling point corresponding to the mid-lactation period.

Time frame: postpartum weeks of 10-20 weeks.

ArmMeasureValue (MEDIAN)
Healthy Breastfeeding WomenMilk Sampling Time Point in the Mid Lactation Period13.9 postpartum weeks
Women With IBDMilk Sampling Time Point in the Mid Lactation Period13.3 postpartum weeks
IBD Subgroup On TNFmAb TreatmentMilk Sampling Time Point in the Mid Lactation Period13.2 postpartum weeks
IBD Subgroup Off TNFmAb TreatmentMilk Sampling Time Point in the Mid Lactation Period13.5 postpartum weeks
Comparison: This is to confirm that there is no difference in the second sampling time points in the mid-lactation period between the groups.p-value: 0.56Wilcoxon (Mann-Whitney)
p-value: 0.51Kruskal-Wallis
Other Pre-specified

Population Pharmacokinetic Study of Anti-TNF Monoclonal Antibody in Milk

Concentrations of anti-TNF monoclonal antibody in milk will be measured once the method is validated. The data will be analyzed using population pharmacokinetic modeling.

Time frame: 1-2 months

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026