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Sleep, Lipids, Insulin & Exercise: A New Brain-Health Model

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Manage episode 521954812 series 2993661
内容由Dung Trinh提供。所有播客内容(包括剧集、图形和播客描述)均由 Dung Trinh 或其播客平台合作伙伴直接上传和提供。如果您认为有人在未经您许可的情况下使用您的受版权保护的作品,您可以按照此处概述的流程进行操作https://zh.player.fm/legal

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This episode reframes Alzheimer’s disease by tracing how the plaque-first narrative emerged from rare genetic mutations—and why most age-related cognitive decline is actually driven by systemic metabolic and microvascular health. We break down the evidence across neurodegenerative diseases, highlight what truly predicts risk, and outline four powerful levers that individuals can control today: sleep, lipid management, insulin sensitivity, and exercise.

We begin by mapping the spectrum of Alzheimer’s, Lewy body, Parkinson’s, and vascular dementia, explaining why these conditions often lead to death through complications like aspiration and infection. We clarify the difference between APOE isoforms as probabilistic risk versus deterministic genes such as APP, PSEN1, and PSEN2, which drive rare early-onset disease. We revisit the rise—and unraveling—of the amyloid hypothesis, including failed trials and the controversy that reshaped the field.

Then we turn to what the data supports: cardiology’s APOB as a model biomarker, the role of microvascular injury in the brain, insulin resistance as a driver of neuroinflammation, and the metabolic underpinnings of long-term cognitive decline. We present the four proven pillars of brain protection and outline a practical three-hour weekly plan built around strength training, intervals, and BDNF-boosting movement.

High-volume keywords used: Alzheimer’s prevention, brain health, metabolic health, microvascular disease, insulin resistance, APOE, exercise, dementia risk

Listener Takeaways

  • Why most cognitive decline is metabolic and microvascular—not amyloid-first
  • The difference between APOE risk and deterministic Alzheimer’s genes
  • How sleep, lipids, insulin sensitivity, and exercise protect the brain
  • The role of APOB, glymphatic clearance, and insulin resistance in decline
  • A practical three-hour weekly training plan to lower lifetime risk

Follow for daily longevity and wellness episodes.

This podcast is created by Ai for educational and entertainment purposes only and does not constitute professional medical or health advice. Please talk to your healthcare team for medical advice.

Never miss an episode—subscribe on your favorite podcast app!

  continue reading

章节

1. Setting The Mission (00:00:00)

2. Mapping Neurodegenerative Diseases (00:00:20)

3. How These Diseases Kill (00:02:11)

4. Genetics And APOE Risk (00:03:25)

5. Deterministic Genes And Amyloid (00:06:03)

6. The Amyloid Crisis And Scandal (00:07:28)

7. Cardiometabolic Biomarkers Vs Brain Markers (00:08:38)

8. The Four Modifiable Pillars (00:09:35)

9. Sleep And The Glymphatic Flush (00:11:05)

10. Lipids, APOB, And Brain Vessels (00:12:05)

11. Insulin Sensitivity And Type 3 Diabetes (00:13:10)

12. Exercise, BDNF, And A Three‑Hour Plan (00:14:10)

313集单集

Artwork
icon分享
 
Manage episode 521954812 series 2993661
内容由Dung Trinh提供。所有播客内容(包括剧集、图形和播客描述)均由 Dung Trinh 或其播客平台合作伙伴直接上传和提供。如果您认为有人在未经您许可的情况下使用您的受版权保护的作品,您可以按照此处概述的流程进行操作https://zh.player.fm/legal

Send us a text

This episode reframes Alzheimer’s disease by tracing how the plaque-first narrative emerged from rare genetic mutations—and why most age-related cognitive decline is actually driven by systemic metabolic and microvascular health. We break down the evidence across neurodegenerative diseases, highlight what truly predicts risk, and outline four powerful levers that individuals can control today: sleep, lipid management, insulin sensitivity, and exercise.

We begin by mapping the spectrum of Alzheimer’s, Lewy body, Parkinson’s, and vascular dementia, explaining why these conditions often lead to death through complications like aspiration and infection. We clarify the difference between APOE isoforms as probabilistic risk versus deterministic genes such as APP, PSEN1, and PSEN2, which drive rare early-onset disease. We revisit the rise—and unraveling—of the amyloid hypothesis, including failed trials and the controversy that reshaped the field.

Then we turn to what the data supports: cardiology’s APOB as a model biomarker, the role of microvascular injury in the brain, insulin resistance as a driver of neuroinflammation, and the metabolic underpinnings of long-term cognitive decline. We present the four proven pillars of brain protection and outline a practical three-hour weekly plan built around strength training, intervals, and BDNF-boosting movement.

High-volume keywords used: Alzheimer’s prevention, brain health, metabolic health, microvascular disease, insulin resistance, APOE, exercise, dementia risk

Listener Takeaways

  • Why most cognitive decline is metabolic and microvascular—not amyloid-first
  • The difference between APOE risk and deterministic Alzheimer’s genes
  • How sleep, lipids, insulin sensitivity, and exercise protect the brain
  • The role of APOB, glymphatic clearance, and insulin resistance in decline
  • A practical three-hour weekly training plan to lower lifetime risk

Follow for daily longevity and wellness episodes.

This podcast is created by Ai for educational and entertainment purposes only and does not constitute professional medical or health advice. Please talk to your healthcare team for medical advice.

Never miss an episode—subscribe on your favorite podcast app!

  continue reading

章节

1. Setting The Mission (00:00:00)

2. Mapping Neurodegenerative Diseases (00:00:20)

3. How These Diseases Kill (00:02:11)

4. Genetics And APOE Risk (00:03:25)

5. Deterministic Genes And Amyloid (00:06:03)

6. The Amyloid Crisis And Scandal (00:07:28)

7. Cardiometabolic Biomarkers Vs Brain Markers (00:08:38)

8. The Four Modifiable Pillars (00:09:35)

9. Sleep And The Glymphatic Flush (00:11:05)

10. Lipids, APOB, And Brain Vessels (00:12:05)

11. Insulin Sensitivity And Type 3 Diabetes (00:13:10)

12. Exercise, BDNF, And A Three‑Hour Plan (00:14:10)

313集单集

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