The Effect of Periconceptional Phthalates Exposure on Couples' Reproductive Health

Tongji Hospital

Status: Unknown

Conditions: Environmental Exposure; Infertility

Study type: Observational

Funder types: Other

Identifiers

NCT03679000

H0425

Details and patient eligibility

About

The study is a prospective cohort study, which is aiming to explore periconceptional phthalates exposure and its potential epigenetic effect on fertility, embryo development, and neonatal outcomes.

Full description

The study is a prospective cohort study, and its subjects are childbearing couples who are seeking assisted reproductive technologies for having a baby in the reproductive center in Tongji Hospital.

1. All enrolled couples will be needed to sign an informed consent and complete a questionnaire for collecting information about demographics, life-style, and medical and reproductive histories.
2. Biological samples will be collected from the participants to measure phthalates metabolites in order to evaluate the exposure of single person or the couple in different time phase.The samples include urine, blood that will be left after the hormones measurement for both spouses. The follicular fluid will be obtained from females on the day of oocyte retrieval. The left sperm samples after sperm analysis will be obtained from men. In the reproductive center of Tongji Hospital, hormone measurement for women and sperm analysis for men are required for the In vitro fertilization and embryo transfer in order to evaluate the fertility of couples.And the blastocyst culture medium will be obtained from couples after blastocyst transfer. All samples will be stored at -80℃ until further analysis.
3. Measurements of phthalates metabolites in the biological samples.
4. Collecting data from electronic medical records and follow-up.The basic information, clinical data and reproductive outcomes of the subjects will be collected by reviewing the electronic medical charts, including the height, weight, basic hormone levels, stimulation protocol and time, insemination protocol, fertilization rate, cleavage rate, excellent embryo rate, blastocyst formation rate, clinical pregnancy rate, as well as live birth rate，the newborns' height, weight, and gestational age, etc.
5. Analyze the miRNA expression profiles of blastocyst culture medium.
6. Statistical analysis. The investigators will analyze the association between the couples' phthalates exposure levels and the reproductive outcomes, and explore the association among periconceptional phthalates exposure, epigenetic changes and reproductive outcomes.

Enrollment: 2,122 estimated patients

Sex: All

Ages: 20 to 45 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

一. Inclusion and exclusion criteria for primary study:

The exclusion of men:

1. Occupational exposures

2. Couples living in separate places

3. Congenital diseases

   • Congenital azoospermia
   • Ejaculation dysfunction
   • Family history of genetic diseases

4. Acquired diseases

   • Genitourinary infections
   • Mumps
   • Endocrine diseases
   • Sexually transmitted diseases
   • Hyperthyroidism
   • Liver failure
   • Renal failure
   • Neurological diseases
   • Paraplegia
   • Acquired testicular injury

5. Patient who have received surgeries：

   • Inguinal hernia surgery
   • Vasectomy
   • Bladder neck surgery
   • Pelvic surgery

6. Patients who have used antitumor drugs and hormone

The exclusion of women:

1. Occupational exposures

2. Couples living in separate places

3. Congenital gonadal dysplasia

   • Genital malformation
   • Chromosomal abnormalities
   • Family history of genetic diseases

4. Endocrine and metabolic diseases

   • Diabetes
   • Hyperprolactinemia
   • Thyroid and adrenal diseases

5. Cardiovascular diseases

   • Dyslipidemia
   • Systemic lupus erythematosus
   • Other rheumatic immune diseases

6. Patients who have received the following treatment:

   • Ovarian surgery
   • Thyroid surgery
   • Pituitary surgery
   • Anti-tumor radiotherapy
   • Chemotherapy

7. Patients with previous history as followed:

   • Endometrial injury
   • Endometrial polyps
   • Endometritis
   • Uterine fibroids
   • Endometriosis

8. Tubal effusion

二. Inclusive and exclusive criteria for blastocyst culture medium collection at the later stage.

Inclusion criteria:

1. Subjects in the primary part of the study

2. ·Normal gender of men and women

   • No genetic diseases or congenital diseases
   • No family genetic history

3. Normal sperm analysis for men

4. Female age <35 years

5. ·Normal Ovarian function for women

   • Normal endocrine function for women
   • No uterine disease or abnormality

6. The causes of infertility :

   • Tubal factors
   • Unexplained

7. The protocol of controlled ovary hyperstimulation :

   • A routine long-term protocol

Exclusion criteria:

1. Subjects with smoking or alcohol abuse in the past 3 months
2. Patients with overweight or obesity (BMI ≥ 25)
3. Embryos with chromosomal abnormalities confirmed by PGS

Trial design

2,122 participants in 1 patient group

The reproductive health of couples

Description:

The study is a prospective cohort study, and its participants are childbearing couples who are seeking assisted reproductive technologies for having a baby in the reproductive center in Tongji Hospital.The study is a observational study.