I wanted to start a thread on plasmalogens, as they are particularly interesting when it comes to both general health and specific health conditions. They have been mentioned in this thread: Health Protocol for Mandatory Coronavirus Vaccination
It should also be noted that the natural production of them declines with age, may be reduced in some due to genetic conditions, and can (most promisingly) hold off things like dementia/Alzheimer's and Parkinson's disease.
Here's an AI overview to start with - although it doesn't cover some of the more interesting aspects. For those who have an understanding of biology the parts I've highlighted should stand out:
Before getting into the details, I've been taking plasmalogens (specifically Mind+ as they are liposomal, and digestion will otherwise break them down) as both a general experiment (and because dementia runs in my family) for over a month now.
My observations are as follows:
I suspect that the improvement to cellular membranes has allowed the TTFD to transfer to cells more easily and improved it's effectiveness/potential.
Better communication and transport of molecules in/out of cells is going to have a profound impact in all aspects of health.
So after observing all that I've dug into some of the data. First an overview of some of the more interesting scientific studies:
AI summary:
That the synapses of the brain need flexible cellular membranes (characterised by enough plasmalogens) in order to properly release acetylcholine is of interest. It would suggest that this could be linked to other learning and memory disorders. And perhaps a similar mechanism for other neurotransmitters and hormones in general.
As well as cellular membranes, plasmalogens seem to protect mitochondrial membrane fluidity as well.
A very detailed summary from Oct 2021 on plasmalogens covering most known pathologies is available here:
www.frontiersin.org
It should also be noted that the natural production of them declines with age, may be reduced in some due to genetic conditions, and can (most promisingly) hold off things like dementia/Alzheimer's and Parkinson's disease.
Here's an AI overview to start with - although it doesn't cover some of the more interesting aspects. For those who have an understanding of biology the parts I've highlighted should stand out:
Plasmalogens are a subclass of phospholipids found in cell membranes, characterized by a vinyl ether bond at the sn-1 position of the glycerol backbone. They are particularly abundant in certain tissues like the brain, heart, and kidneys. Plasmalogens play roles in membrane integrity, signaling, and protecting against oxidative stress.
Key Characteristics:
Biological Functions:
- Vinyl Ether Bond:
The defining feature of plasmalogens is a vinyl ether bond at the sn-1 position of the glycerol backbone, unlike conventional phospholipids which have acyl bonds in that position.
- Broad Distribution:
Plasmalogens are found in various organisms, including bacteria, protozoa, invertebrates, and vertebrates. They are particularly abundant in anaerobic bacteria and certain mammalian tissues.
- Membrane Component:
They are a significant component of cell membranes, contributing to their structure and function.
- Antioxidant Properties:
Plasmalogens have been shown to protect cells from damage caused by reactive oxygen species and may play a role in protecting other lipids and lipoproteins from oxidative stress.
- Signaling and Membrane Dynamics:
They have been implicated in cellular signaling pathways and modulating membrane dynamics.
- Association with Disease:
Research suggests that plasmalogen levels may be associated with various diseases, including neurodegenerative disorders, and that their deficiency can contribute to certain metabolic and inflammatory conditions.
Clinical Significance:
- Membrane Integrity:
Plasmalogens contribute to the structure and stability of cell membranes.
- Oxidative Stress Protection:
They can protect cells from damage caused by reactive oxygen species and oxidative stress.
- Signaling and Membrane Dynamics:
They may be involved in signaling pathways and modulating membrane fluidity.
- Potential Therapeutic Target:
Research suggests that plasmalogens may have therapeutic potential for certain diseases, including neurodegenerative disorders.
- Deficiency in Peroxisomal Disorders:
Deficiency of plasmalogens can occur in peroxisomal disorders like Zellweger syndrome and Rhizomelic chondrodysplasia punctata.
- Association with Alzheimer's Disease:
Some studies suggest that lower plasmalogen levels in the brain may be associated with Alzheimer's disease, and that plasmalogen supplementation may have some cognitive benefits.
- Potential Therapeutic Use:
Oral administration of plasmalogens has been proposed as a potential treatment for certain diseases, including Alzheimer's disease.
Before getting into the details, I've been taking plasmalogens (specifically Mind+ as they are liposomal, and digestion will otherwise break them down) as both a general experiment (and because dementia runs in my family) for over a month now.
My observations are as follows:
- Dreams that indicate higher melatonin (or being more sensitive to melatonin).
- Not smoking as much which would indicate higher acetylcholine (or more sensitivity to acetylcholine).
- More mood stabilisation during the day and night - specifically not rushing into fight/flight in nightmares (so maybe serotonin? and/or better vagal control, so acetylcholine).
- A change in dream 'flavour' (which I didn't get with just melatonin when I took that some time ago) - dreams are in more green/outdoor locations/more expansive as well as being more vivid.
- Apparently a small loss of visceral body fat (according to my scales which measure that)/reduced belly size.
- At the gym I've noticed quite a large improvement in aerobic capacity.
I suspect that the improvement to cellular membranes has allowed the TTFD to transfer to cells more easily and improved it's effectiveness/potential.
Better communication and transport of molecules in/out of cells is going to have a profound impact in all aspects of health.
So after observing all that I've dug into some of the data. First an overview of some of the more interesting scientific studies:
AI summary:
Plasmalogen Webinar Summary
Introduction to Plasmalogens
Plasmalogens are essential but little-known cellular building blocks crucial for health. They play a fundamental role in maintaining healthy cells, which underpin the entire body’s function. Cells contain organelles like peroxisomes and mitochondria for processing materials, and their membranes—composed of fats and proteins—regulate cellular entry and exit. Healthy cell membranes ensure overall cell health, underscoring plasmalogens’ importance in brain, nerve, heart, kidney, and eye function. Plasmalogen levels decline with age due to reduced peroxisome activity.
Role in Brain Health and Neurological Protection
Plasmalogens are vital for brain function, especially in protecting white and gray matter. Experimental models mimicking multiple sclerosis (via cuprizone) and Parkinson’s disease (via MPTP) demonstrate that plasmalogen supplementation prevents damage and aids recovery. This highlights their protective role against neurodegeneration. Cognitive diseases such as Alzheimer’s dementia are associated with plasmalogen deficiency, with studies indicating boosting plasmalogen reserves could reduce Alzheimer’s incidence by 75%. Plasmalogens modulate immune and inflammatory responses within the brain, particularly calming microglial activation.
Alzheimer’s Disease and Genetic Factors
Alzheimer’s dementia risk is heavily influenced by genetic factors (e.g., APOE4 genotype), but plasmalogen levels profoundly modify disease progression. Research shows that maintaining or increasing phospholipid and plasmalogen levels can prevent or delay cognitive decline, demonstrating a causative link between deficiency and dementia. Plasmalogens derived from different fatty acids (including DHA and EPA) affect brain health differently, emphasizing the importance of both precursor availability and cellular conversion mechanisms.
Cholesterol and Cardiovascular Implications
Plasmalogens influence cholesterol metabolism by enhancing cholesterol export from cells, thus lowering circulating cholesterol and plaque build-up. Studies from institutions like the Baker Institute show plasmalogen supplementation dramatically reduces cholesterol plaques, which were long considered irreversible. Plasmalogens’ impact extends to metabolic conditions such as fatty liver disease, with ongoing research focused on reversal using plasmalogen therapy.
Supplementation Challenges and Strategies
Dietary plasmalogen consumption is inefficient because the stomach digests them readily. The only known natural source with effective plasmalogen content is shark liver oil, which is not widely recommended. Instead, synthetic or bioavailable plasmalogen-boosting supplements can elevate blood and membrane plasmalogen levels effectively. Clinical trials in Alzheimer’s patients show cognitive and mobility improvements after several months of supplementation, supporting the potential for therapeutic use. Optimal strategies involve an initial loading phase at higher doses followed by maintenance dosing.
Cell Membrane Structure and Function
Plasmalogens contain a unique vinyl ether bond that contributes to cell membrane fluidity and elasticity, critical for regulating molecular traffic and protecting membrane fats from oxidative damage. This membrane flexibility facilitates neurotransmitter release, notably acetylcholine, essential for memory and cognitive function. Deficiency in plasmalogens leads to rigid membranes, impaired neurotransmitter transmission, and cognitive deficits consistent with dementia.
Human Studies on Cognitive Decline and Longevity
Longitudinal human research confirms that higher plasmalogen (particularly DHA-derived) levels correlate with preserved cognition before death and reduced Alzheimer’s pathology post-mortem. The composition of the cell membrane influences amyloid precursor protein processing—flexible membranes favor protective pathways, whereas rigid, cholesterol-rich membranes promote amyloid plaque formation. Moreover, plasmalogen status strongly predicts dementia risk and overall mortality, with high levels associated with enhanced longevity and lower disease risk.
[note here, that this also included reduced all cause mortality/improved longevity in general]
Gut Microbiome and Additional Biomarkers
Plasmalogen metabolism interacts with gut-derived molecules such as gastrointestinal tract acids (GTAs), which reflect mitochondrial health and inflammation. Good microbiome profiles generate beneficial polyunsaturated fatty acids to support plasmalogen synthesis and healthy aging. GTAs may also serve as markers for bowel cancer risk and neurological disease progression, indicating a broader role for plasmalogen-related pathways.
Clinical Applications and Case Studies
Plasmalogen-boosting supplements have practical applications in reducing cholesterol, improving neurocognitive conditions, and potentially alleviating symptoms in neurological disorders like multiple sclerosis, autism spectrum disorders, and Alzheimer’s disease. Anecdotal reports demonstrate remarkable patient improvements, including restored mobility and cognitive functions. Ongoing webinars and global physician collaborations highlight the emerging clinical utility of plasmalogens.
Conclusion and Further Resources
Plasmalogen science, although discovered decades ago, has only recently yielded practical insights into measurement, supplementation, and therapeutic use. The ability to measure plasmalogen levels and modify them presents a novel frontier in preventive and regenerative medicine. For those wishing to explore the topic more deeply, extensive lecture series and research resources by experts like Professor Gooden provide comprehensive scientific background and clinical perspectives.
Overall Summary:
Plasmalogens are critical lipid components of cell membranes that uphold cellular and neurological health, regulate cholesterol metabolism, and influence aging and longevity. Their decline with age and in disease states like Alzheimer’s dementia makes them a promising target for therapeutic intervention. Supplementation strategies to restore plasmalogen levels may drastically reduce dementia incidence, improve cognitive function, and extend healthy lifespan. Advances in testing and clinical application are rapidly evolving, creating new opportunities to address multiple chronic health challenges by targeting cellular membrane composition directly.
That the synapses of the brain need flexible cellular membranes (characterised by enough plasmalogens) in order to properly release acetylcholine is of interest. It would suggest that this could be linked to other learning and memory disorders. And perhaps a similar mechanism for other neurotransmitters and hormones in general.
As well as cellular membranes, plasmalogens seem to protect mitochondrial membrane fluidity as well.
In Barth syndrome (BTHS) mutations in tafazzin leads to changes in both the quantities and the molecular species of cardiolipin (CL), which are the hallmarks of BTHS. Contrary to the well-established alterations in CL associated with BTHS; recently a marked decrease in the plasmalogen levels in Barth specimens has been identified. To restore the plasmalogen levels, the present study reports the effect of promotion of plasmalogen biosynthesis on the lipidome of lymphoblasts derived from Barth patients as well as on cell viability, mitochondria biogenesis, and mitochondrial membrane potential. High resolution 31P NMR phospholipidomic analysis showed an increase in the levels of plasmenylethanolamine (the major plasmalogen in lymphoblasts), which reached values comparable to the control and a compensatory decrease in the levels of its diacyl-PE counterpart. Importantly, 31P NMR showed a significant increase in the levels of CL, while not altering the levels of monolysocardiolipin. Mass spectrometry measurements showed that the promotion of plasmalogen biosynthesis did not change the molecular species profile of targeted phospholipids. In addition, promotion of plasmalogen biosynthesis did not impact on cellular viability, although it significantly decrease mitochondria copy number and restored mitochondrial membrane potential. Overall, the results showed the efficacy of the promotion of plasmalogen biosynthesis on increasing the CL levels in a BTHS cell model and highlight the potential beneficial effect of a diet supplemented with plasmalogen precursors to BTHS patients.
A very detailed summary from Oct 2021 on plasmalogens covering most known pathologies is available here:

Frontiers | Plasmalogens and Chronic Inflammatory Diseases
It is becoming widely acknowledged that lipids play key roles in cellular function, regulating a variety of biological processes. Lately, a subclass of glyce...
