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The Damage Starts Before the First Breath

BD

Dr. Barry Dublin, MD

June 5, 2026

The Damage Starts Before the First Breath

The Mitochondrial Decline | Part 2 of 5

In Part 1, we introduced the mitochondrion — the power plant inside every cell — and why it matters so much. We described what happens when those power plants start to fail: a slow, cascading energy crisis that affects the brain, the heart, the muscles, the immune system, and nearly every organ in the body. We introduced the idea that the modern chemical environment is stressing these power plants in ways the human body never evolved to handle.

Now we need to ask the harder question: how early does this start?

The answer, supported by a growing body of research, is: before birth.

Microplastics in Every Placenta Tested

In 2024, a study published in Environment International tested human placentas for the presence of microplastics — tiny fragments of plastic, often invisible to the naked eye, that break off from food packaging, water bottles, synthetic clothing, and thousands of other everyday products. The result was not that some placentas contained microplastics. It was that every single one did. One hundred percent of samples tested positive.

Research Finding

"100% of human placentas tested contained microplastics. The barrier between mother and fetus is no longer a barrier."

— Environment International, 2024[1]

This means that the developing fetus — during the most sensitive window of organ formation, brain development, and mitochondrial replication — is already bathing in plastic-derived chemistry. The barrier between mother and fetus, which was once assumed to filter out most environmental contaminants, is no longer functioning as a barrier for these compounds.

PFAS in Cord Blood

PFAS — per- and polyfluoroalkyl substances, often called "forever chemicals" because they do not break down in the environment or in the body — are now detectable in the cord blood of newborns. A 2023 study found that maternal and neonatal PFAS concentrations are closely correlated, meaning that whatever the mother has accumulated, the baby inherits a significant share of it at birth.[2]

PFAS are known endocrine disruptors. They interfere with thyroid function, immune development, and lipid metabolism. But the piece that matters most for this series is what they do to mitochondria.

Measuring Mitochondrial Damage Before Birth

Mitochondrial DNA copy number — the number of mitochondrial genomes per cell — is one of the most reliable biomarkers of mitochondrial health. When cells are under stress, they often increase mtDNA copy number as a compensatory response, trying to maintain energy output from damaged power plants. Think of it as a factory running extra shifts because its machines are breaking down. Later, when the damage becomes severe enough, copy number drops — the factory can no longer keep up.

A 2023 study found that prenatal PFAS exposure was associated with altered mitochondrial DNA copy number in newborns.[3] A separate study found that prenatal air pollution exposure produced similar changes in cord blood mtDNA copy number.[4] A 2024 pediatric study found that PFAS exposure in children was associated with reduced mtDNA copy number.[5] A 2025 mediation study found that PFAS exposure was linked to altered triglycerides through changes in mtDNA copy number — meaning the mitochondrial damage was mediating the metabolic consequences.[6]

The Pattern

PFAS, air pollution, and heavy metals all produce the same measurable biomarker change in newborns: altered mitochondrial DNA copy number. The damage is real, it is measurable, and it is happening before the first breath.

A 2023 study found that exposure to mixtures of heavy metals in children was also associated with altered mtDNA copy number.[7] The pattern is consistent: different toxicants, same mitochondrial target.

The Columbia University Kraków Comparison

One of the most striking bodies of evidence comes from the Columbia Center for Children's Environmental Health, which has been running parallel birth cohort studies in New York City and Kraków, Poland, for over two decades. Both cities had significant air pollution. Both had populations of pregnant women whose exposures could be measured and whose children could be followed over time.

In Kraków, the researchers measured PAH-DNA adducts — molecular evidence that combustion-derived chemicals had physically bound to the DNA of newborns. They found that higher prenatal PAH exposure was associated with reduced head circumference, lower birth weight, and later cognitive deficits in childhood.[8]

In New York City, the same research group found that prenatal exposure to polycyclic aromatic hydrocarbons — from traffic, heating systems, and tobacco smoke — was associated with DNA damage in cord blood, reduced birth weight, smaller head circumference, and later developmental delays and behavioral problems in the children.[9]

The Green Space Data

A 2023 study followed children from birth through age 18 and tracked their mitochondrial DNA copy number over time. The study found that children living in areas with more green space — less traffic pollution, less industrial exposure — maintained healthier mtDNA copy number trajectories throughout childhood and adolescence.[10] The environment the child grows up in continues to shape mitochondrial health long after birth.

The Population-Level Numbers

A 2025 paper in Academic Pediatrics found chronic conditions in American children rose from 22.6 percent in 1999–2000 to over 30.2 percent by 2017–2018 — approximately 130,000 additional affected American children every single year.[11] A 2025 JAMA analysis found chronic conditions rose from 39.9 percent in 2011 to 45.7 percent by 2023.[12] The CDC estimates roughly one in 31 children is on the autism spectrum[13] and more than 7 million have ADHD.[14]

Population Data

Chronic conditions in American children rose from 22.6% to 30.2% in less than two decades — approximately 130,000 additional affected children every single year.

— Academic Pediatrics, 2025[11]

The Shared Biological Fingerprint

A 2024 systematic review found that autism, ADHD, intellectual disability, speech delay, and anxiety in children share a remarkably consistent biological fingerprint: increased oxidative stress, elevated toxic metal burden, decreased methylation capacity, mitochondrial dysfunction, and reduced blood flow to the brain.[16] These appear to be five different expressions of the same underlying cellular energy crisis.

The same biology that can be damaged can also be supported and rebuilt. Mitochondria respond to demand. They respond to clean inputs. They respond to good fuel. They respond to good sleep. The body is not a one-way road into illness. It is a system that listens to what you give it.

In Part 3, we look at the six major doorways through which modern life delivers mitochondrial damage to adults — and what you can do about each one.

Concerned About Your Child's or Your Own Mitochondrial Health?

A discovery call with Dr. Dublin can help you understand what's happening at the cellular level and what practical steps you can take to support mitochondrial function.

Schedule a Discovery Call →

Free Download: The Mitochondrial Toxin Reference Guide

Every toxin category covered in this series — the specific products where each exposure shows up in daily life, practical alternatives, and a structured action guide — in one downloadable reference.

Download Free Guide →

References

1. Microplastics found in every human placenta tested. Environment International. 2024. Link

2. Determinants of maternal and neonatal PFAS concentrations. 2023. Link

3. Prenatal PFAS exposures and newborn mitochondrial DNA copy number. 2023. Link

4. Janssen, B.G. et al. Mitochondrial DNA content in cord blood and prenatal air pollution. Link

5. Pediatric PFAS and mtDNA copy number study. 2024. Link

6. PFAS, triglycerides, and mtDNA copy number mediation study. 2025. Link

7. Metals mixture exposure and mtDNA copy number in children. 2023. Link

8. Columbia Center for Children's Environmental Health. Kraków findings. Link

9. Columbia Center NYC newborn PAH-DNA adduct findings. Link

10. Mitochondrial DNA copy number dynamics in NYC children through age 18. 2023. Link

11. Pediatric-Onset Chronic Conditions 1999–2018. Academic Pediatrics. 2025. Link

12. US Children's Chronic Conditions 2007–2023. JAMA. 2025. Link

13. CDC Autism data. Link

14. CDC ADHD data. Link

15. DOHaD review. Link

16. Mitochondrial dysfunction in neurodevelopmental disorders. Frontiers in Psychiatry. 2024. Link

BD

Dr. Barry Dublin, MD

Physician specializing in metabolic medicine and therapeutic ketosis. Creator of the SKLeTT Protocol — Specific Ketone Level Titration Therapy — and founder of NeuraLift. Over 30 years of clinical experience in brain energy optimization and weight management.