Zinc-AA Supplementation During Pregnancy & Lactation to Assess Effects on ASD Prevalence in Offspring
Primary Purpose
Autism Spectrum Disorder, Zinc Deficiency, Pregnancy Related
Status
Suspended
Phase
Not Applicable
Locations
Mexico
Study Type
Interventional
Intervention
Zn-AA
Sponsored by
About this trial
This is an interventional prevention trial for Autism Spectrum Disorder focused on measuring Zinc supplementation, Pregnancy
Eligibility Criteria
Inclusion Criteria:
- Women from 18 to 35 years of age, pregnant, within the 12th and 20th week (Primary study) or with the intention to get pregnant in the following six months (Secondary study)
- Hemoglobin over 8 g/dL
- Accepting to be included in a standard pediatric physical and neurobehavioral follow-up program from birth and to at least 18 months of age.
- Accepting to receive the Zinc supplement (or placebo) and to ingest it daily from the inclusion to the study and up to the sixth postnatal month
- Agreement to read and sign the Informed Consent Document
Exclusion Criteria:
- Women who do not accept to deliver in a hospital setting, or without immediate access to a proper facility
- Women with self-reported alcohol or drug addiction
- Women with a sero positivity to HIV, even if under treatment
- Women with a pregnancy resulted from assisted or in vitro fertilization techniques
- Women with an active severe acute respiratory syndrome-Coronavirus (SARS-CoV2) infection
Sites / Locations
- Centro Universitario en Salud
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Orange
Green
Arm Description
Zinc-AA, Tablet, 30 mg. PO, Once Daily for up to one year
Placebo, Tablet, 30 mg. PO, Once Daily for up to one year.
Outcomes
Primary Outcome Measures
Autism spectrum disorder
Positive identification of any component of the Autism Spectrum Disorder (ASD) through the Autism Diagnosis Observation Schedule, 2nd edition (ADOS-2) specialized battery of tests, which provide a standardized set of tests that offer as output a set of ranges of concern reflecting the extent to which a child demonstrates behaviors associated with ASD.
Secondary Outcome Measures
Microbiota modification associated to maternal zinc supplementation or placebo during pregnancy
Comparative analysis of the microbiome composition (Type and relative quantity of micro-organisms) in a subset of the supplemented and the un-supplemented groups, at birth, and also at the end of the first six months of lactation
Immune phenotype
Comparison of the Immune phenotype (Type and quantity of main Interleukines and Cytokines in peripheral blood, and characterization of Leucocyte population and subpopulation, also in peripheral blood) in a subset of the supplemented and the un-supplemented groups, at birth, and also at the end of the first six months of lactation
Full Information
NCT ID
NCT04983667
First Posted
July 11, 2021
Last Updated
February 27, 2023
Sponsor
Instituto Tecnologico y de Estudios Superiores de Monterey
1. Study Identification
Unique Protocol Identification Number
NCT04983667
Brief Title
Zinc-AA Supplementation During Pregnancy & Lactation to Assess Effects on ASD Prevalence in Offspring
Official Title
Supplementation of Zinc-AA Complexes in Women During Pregnancy and Lactation, to Assess Effects on Autism Spectrum Disorder (ASD), Immune Status and Gut Microbiota in Offspring
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Suspended
Why Stopped
A funding agreement could not be secured with the primary funding organizations
Study Start Date
May 27, 2021 (Actual)
Primary Completion Date
December 31, 2022 (Actual)
Study Completion Date
December 31, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Instituto Tecnologico y de Estudios Superiores de Monterey
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Autism and associated entities, grouped under the Autism Spectrum Disorders (ASD) is the fastest growing intellectual disability in the world, statistics signal for a 1 to 3% prevalence on infants. The cause is unknown, although some data suggest that zinc deficiency during pregnancy may have an important role in its presentation. This study seeks to supplement the nutrition of randomly selected prospective and actually pregnant women with a zinc-Amino-acid complex (Zn-AA), during pregnancy and early lactation, and compare the rate of ASD in their offspring with the rate in a similar and also randomly selected cohort of non supplemented women, to assess if Zn-AA supplementation during pregnancy has any effect on this outcome
Detailed Description
Autism and associated disorders (Autism Spectrum Disorders, ASD) is the fastest growing disability in the world, statistics indicate a prevalence of between 1 and 3%. This entity is the one that generates more stress in families, four times more than in a neuro-typical family and twice more than in a family with any other disability. Besides, this condition increases health spending for the family, the state and the country.
By not knowing the cause, and witnessing the growth of this disability, with the prevalence described, and the births reported in 2019 in Mexico (2,092,214), we expect between 20,922 and 62,766 new cases in our country each year. In Nuevo León, a state in the northeast of Mexico, the average birth rate per year from 2017 to 2019 (latest official data available) is 91,484, which makes us estimate an incidence of 915 to 2744, for the same period. ASD is also a family stressful disability, associated to a high rate of separations, social isolation and divorces, which leads to social problems of alarming dimensions. In the United States, for 2025 the cost of Autism is projected at 1 trillion dollars, associated with medications, interventions and educational expenses.
In Mexico, the lack of universal diagnostic screening, detection and intervention programs before the age of three years makes those affected to require important support throughout their lives, since the benefits of early intervention are lost.
This project consists of two parts. The first is the Primary Study. It consists of establishing whether the supplementation of Zinc-AA complexes, in women during pregnancy and lactation, has any effect on the prevalence of Autism and if it favorably modifies the immunological and metabolic status of the mother and the progeny; seeks to confirm the findings that our group of investigators has obtained in published pre-clinical investigations that found that a Zinc deficiency in the mother (mice and human erythrocytes), caused by dietary factors, provokes changes in the morphology of the intestine of the progeny, as well as modifications in the microbiota and increased inflammatory markers in the blood and brain, similar to those reported in people with Autism. In Latin America, the diet is based on cereals, and i so abundant in dietary fiber and phytates. These factors, along supplements usually recommended to mothers who plan to become pregnant (Calcium, Iron and Folic Acid), predispose these women to Zinc deficiency. We are also proposing a Secondary Study, to establish the zinc status and the characteristics of the intestinal microbiome in young, non-pregnant adult women, as a comparative reference standard.
Until now, there are no projects in the world that seek to partially or totally solve the causes of Autism, this is the first study that seeks to prevent the problems associated with autism and could be the first to influence the reduction of the incidence of Autism. This project will involve Mexican researchers from Instituto Tecnologico y de Estudios Superiores de Monterrey (ITESM), as well as researchers from the University of Limerick, Ireland, from the University Clinic of the Autonomous University of Nuevo León, in the northeast of Mexico; as well as the Laboratory of Dr. Fanis Missirlis, of the National Polytechnic Institute, in Mexico City.
This project has the financial support of the International Zinc Association (IZA), managed by Zinpro Corp., represented in Mexico by Elemend Salud, representative Ing. Guillermo Vela Staines (g.vela@zinpro.com).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Autism Spectrum Disorder, Zinc Deficiency, Pregnancy Related
Keywords
Zinc supplementation, Pregnancy
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Parallel 1:1 randomization to one of two interventions, the active compound or the placebo
Masking
ParticipantCare ProviderOutcomes Assessor
Masking Description
Randomized allocation to one of two supplements, one has the active compound, the other is a placebo. Identical containers and labels have been designed. Both groups will receive the customary iron sulfate and folic acid supplementation along pregnancy
Allocation
Randomized
Enrollment
3840 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Orange
Arm Type
Experimental
Arm Description
Zinc-AA, Tablet, 30 mg. PO, Once Daily for up to one year
Arm Title
Green
Arm Type
Placebo Comparator
Arm Description
Placebo, Tablet, 30 mg. PO, Once Daily for up to one year.
Intervention Type
Dietary Supplement
Intervention Name(s)
Zn-AA
Intervention Description
Oral supplementation of either 30 mg daily or Zinc-AA complex or placebo, from the study recruitment during first trimester of pregnancy, all through pregnancy and up to the sixth month after giving birth.
Primary Outcome Measure Information:
Title
Autism spectrum disorder
Description
Positive identification of any component of the Autism Spectrum Disorder (ASD) through the Autism Diagnosis Observation Schedule, 2nd edition (ADOS-2) specialized battery of tests, which provide a standardized set of tests that offer as output a set of ranges of concern reflecting the extent to which a child demonstrates behaviors associated with ASD.
Time Frame
From 16 to 20 months of age
Secondary Outcome Measure Information:
Title
Microbiota modification associated to maternal zinc supplementation or placebo during pregnancy
Description
Comparative analysis of the microbiome composition (Type and relative quantity of micro-organisms) in a subset of the supplemented and the un-supplemented groups, at birth, and also at the end of the first six months of lactation
Time Frame
From birth to six months of age
Title
Immune phenotype
Description
Comparison of the Immune phenotype (Type and quantity of main Interleukines and Cytokines in peripheral blood, and characterization of Leucocyte population and subpopulation, also in peripheral blood) in a subset of the supplemented and the un-supplemented groups, at birth, and also at the end of the first six months of lactation
Time Frame
From birth to six months of age
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Women from 18 to 35 years of age, pregnant, within the 12th and 20th week (Primary study) or with the intention to get pregnant in the following six months (Secondary study)
Hemoglobin over 8 g/dL
Accepting to be included in a standard pediatric physical and neurobehavioral follow-up program from birth and to at least 18 months of age.
Accepting to receive the Zinc supplement (or placebo) and to ingest it daily from the inclusion to the study and up to the sixth postnatal month
Agreement to read and sign the Informed Consent Document
Exclusion Criteria:
Women who do not accept to deliver in a hospital setting, or without immediate access to a proper facility
Women with self-reported alcohol or drug addiction
Women with a sero positivity to HIV, even if under treatment
Women with a pregnancy resulted from assisted or in vitro fertilization techniques
Women with an active severe acute respiratory syndrome-Coronavirus (SARS-CoV2) infection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rebeca Thelma Martínez-Villarreal, M.D., Ph:D.
Organizational Affiliation
Universidad Autónoma de Nuevo León, Centro Universitario de Salud, Campus de la Salud
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centro Universitario en Salud
City
San Nicolás De Los Garza
State/Province
Nuevo Leon
ZIP/Postal Code
64451
Country
Mexico
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Data will be archived in the Institutional Repository
IPD Sharing Time Frame
One year upon completion
IPD Sharing Access Criteria
To qualified health researchers upon request, all data will be anonymized.
Learn more about this trial
Zinc-AA Supplementation During Pregnancy & Lactation to Assess Effects on ASD Prevalence in Offspring
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