Impact of Metabolic Health on Sperm Epigenetic Marks in Humans

Type 2 Diabetes Mellitus Clinical Trial

Official title:

Impact of Metabolic Health on Sperm Epigenetic Marks in Humans

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03860558
• Other study ID #: 2015-40
• Status: Recruiting
• Phase: N/A
• Start date: May 1, 2018
• Est. completion date: July 1, 2024

Study information

• Verified date: August 2023
• Source: Joslin Diabetes Center
• Contact: Mary E Patti, MD
• Phone: 6173092635
• Email: mary.elizabeth.patti[@]joslin.harvard.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study is designed to evaluate whether epigenetic markers in overweight men with type 1 diabetes (T1D) or type 2 diabetes (T2D) can be improved with a 3 month lifestyle intervention or program focused in glycemic intervention.

Description:

Parental history of diabetes confers substantial individual risk for development of obesity and diabetes. Obesity risk can be transmitted across generations, from parents or grandparents to children. Genomic variation explains only a portion of this risk. Epigenetic modulation through DNA methylation, histone modification, or by noncoding RNAs, provide mechanisms to regulate gene activity independent of DNA sequence by determining which genes are turned on or off in response to environment or disease. Epigenetic changes can be stable over the lifespan providing a mechanism through which environmental exposures may impart long-term effects on gene expression and phenotypic outcome.

The maternal intrauterine environment is now well recognized to modify obesity and T2D disease risk of offspring. Fetuses carried by women who are obese, have diabetes, or suffer from suboptimal nutrition are at increased risk of insulin resistance, obesity, T2D, and cardiovascular disease risk as adults. Studies in rodents also show that the health, metabolism, and prior environmental exposures of the male can also influence health of his offspring. Existing data provide powerful support for the hypothesis that current glucose levels and overall metabolic health of males can alter epigenetic marks in sperm and suggest a novel modifiable mechanism of transmission. However, much less is known about how human sperm epigenetic patterns change with nutritional and metabolic health, and whether these may ultimately impart differences in health of future generations. Thus, we are studying the impact of both type 1 and type 2 diabetes, and elevations in glucose common to both conditions, on human reproductive health and the sperm epigenome.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 40
• Est. completion date: July 1, 2024
• Est. primary completion date: July 1, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Male, age 18-65 years

• Willing and able to provide informed consent and follow all study procedures, including providing sperm specimens 3 months apart.

• Type 1 or type 2 diabetes diagnosis confirmed by an endocrinologist (for participants in the diabetes groups)

• HbA1c > 7% (for participants in the diabetes groups)

• Overweight (BMI > 25 kg/m2) (for all groups, to ensure groups are similar)

Exclusion Criteria:

• Chronic kidney disease stage 4 or 5 (including end-stage renal disease);

• Hepatic disease, including serum alanine transaminase (ALT) or aspartate aminotransferase (AST) greater than or equal to 3 times the upper limit of normal; hepatic synthetic insufficiency as defined as serum albumin < 3.0 g/dL; or serum bilirubin > 2.0;

• Severe diabetic retinopathy;

• Congestive heart failure, New York Heart Association (NYHA) class II, III or IV;

• History of myocardial infarction, unstable angina or revascularization within the past 6 months;

• Active genitourinary infection;

• Testicular volume <12 mL (assessed using Prader orchidometer);

• Hypogonadism, defined as total testosterone <250 ng/dl;

• Hyperprolactinemia, defined as prolactin >18 ng/ml;

• Hyperestrogenism, defined as estradiol >42 pg/ml;

• Cryptorchidism;

• Cigarette smoking;

• Active alcohol abuse or substance abuse;

• Cancer (except localized non-melanoma skin cancers) or use of chemotherapy agents within 5 years;

• Use of nitrates or guanylate cyclase stimulators;

• Use of steroid hormones (including testosterone), other than inhalers for reactive airway disease

Related Conditions & MeSH terms

• Diabetes Mellitus
• Diabetes Mellitus, Type 1
• Diabetes Mellitus, Type 2
• Overweight
• Type 1 Diabetes Mellitus
• Type 2 Diabetes Mellitus

Intervention

Other:
• Lifestyle Intervention
Participants will undergo a 12-week multidisciplinary program for weight control and intensive diabetes management. The program includes adjustments to diabetes medications to enhance weight reduction and improve glycemia, dietary modification, and activity instructions.
• No Intervention
Participants will not undergo an intervention.

Locations

Country	Name	City	State
United States	Joslin Diabetes Center	Boston	Massachusetts

Sponsors (1)

Lead Sponsor	Collaborator
Joslin Diabetes Center

Country where clinical trial is conducted

United States, 

References & Publications (1)

Sales VM, Ferguson-Smith AC, Patti ME. Epigenetic Mechanisms of Transmission of Metabolic Disease across Generations. Cell Metab. 2017 Mar 7;25(3):559-571. doi: 10.1016/j.cmet.2017.02.016. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Spermatozoa concentration	Sperm will be assessed for concentration, reported as total yield (millions per ml)	1 year
Secondary	Sperm DNA methylation, reported as genomic location of regions with methylation altered in response to intervention	We will utilize purified DNA (1.5 µg), sheared by sonication to obtain 200-700 bp fragments for subsequent library preparation for methylation-dependent immunoprecipitation and sequencing. Differentially methylated regions (DMR) are identified using methylated DNA immunoprecipitation coupled with next-generation sequencing (MEDIPS). DNA methylation is assessed using sliding windows (500 bp size, 200 bp shift). Regions with read ratios >1.5 or <0.67 and binomial p<0.0001 in independent biologically replicated comparisons are designated as DMR.	1 year
Secondary	RNA Sequencing	RNA will be isolated from sperm samples and subjected to RNA sequencing to analyze the content of both of large messenger ribonucleic acid (mRNA)/noncoding RNA and small RNAs. Data will be analyzed to identify those species altered in response to intervention.	1 year