Inspired, by Clara Vinter

Hi, I’m Clara Vinter -a registered nurse from Sweden with a deep curiosity for how our genes shape the way we live, feel, and move through the world.

Last year, I took a genetic test, in search for a grandparent gone, mostly out of curiosity. 

What I discovered sparked a deeper interest in how our genes may influence everything from how we metabolize nutrients to how we handle stress or respond to different environments. What started as a personal interest quickly grew into a deeper fascination with how our DNA might influence everything.

Please know that nothing I write should be taken as medical advice. I’m not a doctor, and genetic research is evolving fast. My aim is to inspire reflection, not diagnosis.

If you're curious about your own biology, love learning about health in a holistic way, or simply want to follow someone who’s exploring the same questions  -you’re warmly invited to join me on this journey.

 

Let’s stay curious together.
- Clara

The blog from Clara Vinter
-Trapped Behind Glass: How Our Genes Shape the Feeling of Being Excluded?

 

By Clara Vinter, RN, writer, 8 min read

2025-04-30

“Love is always the answer.”

Disclaimer: I am a registered nurse, from Sweden, not a physician or licensed geneticist. The information provided in this article is for educational purposes only and is not intended to diagnose, treat, or prevent any disease. Always consult with a qualified healthcare professional before making any medical decisions or changes to your treatment plan based on genetic information.

 

Ever Felt Like You’re Behind an Invisible Wall?

You’re physically there, in the room, part of the group.
But emotionally, it’s like watching everything happen behind soundproof glass.

Conversations feel distant.
Laughter doesn’t quite reach you.
A sense of exclusion settles in, even when no one’s intentionally pushing you away.

If this resonates, you’re not alone -and you’re not imagining it. New insights from genetic research are beginning to shed light on why some people experience social distance more acutely than others. One key player? A gene called OXTR.

The OXTR Gene: Rewiring How We Feel Connection

The OXTR gene encodes the oxytocin receptor, which is like a lock that opens in response to oxytocin, the hormone often nicknamed the “love hormone.”

Oxytocin influences:

  • Social bonding
  • Trust and empathy
  • Emotional regulation
  • Sensitivity to social cues

One variation in this gene, known as rs53576, has been linked to how we respond to social experiences.

  • People with the GG genotype may be more emotionally resilient, socially confident, and trusting.
  • Those with AG or AA genotypes tend to be more sensitive to social stress and more reactive to feelings of exclusion or rejection.

But this sensitivity is not a weakness -it’s a feature. In safe, supportive environments, it can make someone more empathic, perceptive, and caring. In hostile or emotionally cold settings, it can make someone feel deeply alone.

 

 

feeling like in a bubble?

Other Genes That May Influence Social Sensitivity

OXTR doesn’t act in isolation. Our experience of the social world is shaped by a network of genes interacting with our environment. Some others worth mentioning:

🧬 SLC6A4 -The Serotonin Transporter Gene

  • Variant: 5-HTTLPR (short allele)
  • Linked to: increased sensitivity to social rejection, anxiety, and depression
  • Known for shaping how we respond to emotional challenges and perceived threats

🧬 COMT, Catechol-O-Methyltransferase

  • Variant: Val158Met (Met/Met genotype)
  • Influences: how quickly dopamine is cleared from the brain
  • Associated with deeper emotional processing and slower recovery from stress or conflict

🧬 DRD4 / DRD2, Dopamine Receptor Genes

  • Involved in: motivation, reward, novelty-seeking
  • Variants may influence how rewarding social interaction feels -or how uncomfortable unpredictability is

🧬 AVPR1A -Vasopressin Receptor

  • Affects social bonding, especially attachment and monogamous behavior in some species
  • Human studies suggest a potential role in emotional closeness and pair bonding

Together, these genes may predispose some of us to feel more deeply, connect more cautiously, or struggle more with rejection, even if outwardly, everything seems “fine.”

You’re Not Broken, You’re Tuned Differently

Let’s get one thing clear: genetics is not destiny.

Having a certain variant doesn’t doom you to loneliness or anxiety. But it might help explain why you feel the way you do, and reduce the shame that often comes with it.

Think of a highly sensitive nervous system as a smoke detector set to “high alert.” It’s useful in dangerous environments. But in a safe room, it can become overwhelming.

Learning how your brain and body are wired can:

  • Reduce self-blame
  • Inform your self-care choices
  • Guide you to environments and people who support your well-being

 

Practical Steps for the Socially Sensitive

If you’re beginning to see yourself in this story, here are some gentle steps to explore:

1. Validate your experience.

Just because others don’t feel it doesn’t mean it’s not real. Trust your internal signals.

2. Explore genetic testing, if you feel ready.

Services like X or X can provide raw data. Tools like X or X can help interpret it (note: always do this cautiously and never in isolation).

3. Create a supportive environment.

That might mean fewer large gatherings, more meaningful one-on-one connections, or time alone to recharge. You don’t need to apologize for how you’re wired.

4. Practice radical self-compassion.

Feelings of exclusion hurt. But if you know they arise more easily in your system, you can begin to meet yourself with understanding instead of self-judgment.

 

Why I Wrote This

As a nurse, I’ve witnessed how invisible emotional wounds shape people’s lives. I’ve also sometimes wrestled with these feelings myself. For years, I thought I just “wasn’t trying hard enough, or, maybe they don´t like me?” in social situations, until I discovered that my biology was playing a role.

Neither is inherently better. It depends entirely on the context, environment, and what kind of life or relationships a person values.

Here’s a comparison to clarify:

🔹 Higher Sensitivity (e.g., OXTR AA/AG)

Pros:

Deep empathy and attunement to others

Strong intuition about emotional dynamics

Greater social awareness and caution

Likely to notice when others are distressed or excluded

Cons:

More vulnerable to social rejection and criticism

Higher risk for anxiety, depression, and emotional burnout

May struggle in high-conflict or emotionally chaotic environments

🔹 Lower Sensitivity (e.g., OXTR GG)

Pros:

Emotionally resilient and socially confident

Less affected by negative social feedback

Often good leaders or initiators in group settings

Thrive in competitive or unpredictable environments

Cons:

May miss subtle emotional cues

Risk of seeming emotionally distant or insensitive

Less likely to notice or respond to others’ emotional needs

The Bottom Line:

  • In a nurturing, emotionally rich environment, higher sensitivity can be a superpower.
  • In a harsh, fast-paced, or emotionally cold environment, lower sensitivity can be protective.

So the key is self-awareness: knowing how you’re wired and shaping your environment, relationships, and self-care to match your biology.

Sensitivity & Social Genetics: What’s Better?

Trait

Higher Sensitivity (OXTR AA/AG)

Lower Sensitivity (OXTR GG)

Empathy

Deep, intuitive, emotionally attuned

Present but less intense, more cognitive

Social Awareness

Highly tuned to others’ moods and cues

May miss subtle signals

Emotional Resilience

Lower, feels rejection deeply

Higher, brushes off social stress

Trust in Others

More cautious, can take time

Generally more trusting

Stress Response

More reactive, especially to conflict

More stable under pressure

Strengths

Empathy, intuition, emotional depth

Confidence, leadership, adaptability

Challenges

Risk of overwhelm, anxiety, withdrawal

Risk of insensitivity, missing nuance

 

 

🌱 There’s No One “Best” -Only What’s Best for You

Whether you’re highly sensitive or more resilient by nature, the goal isn’t to fix yourself, it’s to understand yourself. That’s where growth begins.

This article is not about pathologizing sensitivity, it’s about honoring it. Understanding how we’re wired can be a powerful tool for healing, connection, and even personal empowerment.

And when in doubt?

Love is always the answer.

- Clara Vinter, RN

#Genetics #Neurodiversity #MentalHealth #SocialConnection #OXTR #Genes #ClaraVinterWriter #ClaraVinterWellness

The blog from Clara Vinter

Ozempic, Wegovy, Zepbound, and the Future of Health: A Scandinavian Nurse’s Perspective

 Ozempic, and the Future of Health: A Scandinavian Nurse’s Perspective

Ozempic, Wegovy, Zepbound, and the Future of Health: A Scandinavian Nurse’s Perspective

Clara Vinter

2025-04-26

By Clara Vinter, Swedish nurse and writer

 

As a nurse from Sweden, I’ve had a front-row seat to one of the most fascinating health phenomena of our time: the global rise of Ozempic, and now Wegovy and Zepbound (Tirzepatid), medications reshaping the conversation around weight management and metabolic health.

Have I tried it? I might have!?

Developed by the Danish company Novo Nordisk, Ozempic (semaglutide) was originally designed to help people with type 2 diabetes manage their blood sugar. But its unexpected side effect, significant weight loss, captured worldwide attention, from Hollywood to health clinics across Europe.
Now, its sibling drug Wegovy (also semaglutide but at a higher dose) is specifically approved for chronic weight management. Meanwhile, Eli Lilly’s Zepbound (tirzepatide), recently approved in the U.S. and expanding globally, offers a new generation of multi-pathway treatments targeting both GLP-1 and GIP receptors.

Being Scandinavian, I find it particularly inspiring that breakthroughs like these come from our region, especially Denmark, just across the Öresund Bridge. It reminds us that even smaller countries can lead global health innovation.

But beyond the headlines, a deeper question intrigues me:
Are our genes playing a role in how we respond to these new medications?
And what could that mean for the future of personalized health?

What We Know About GLP-1 Drugs and Genetics So Far

Ozempic, Wegovy, and Zepbound work primarily by mimicking natural hormones (GLP-1, and in Zepbound’s case, also GIP) that regulate appetite, blood sugar, and metabolism.
They slow gastric emptying, promote feelings of fullness, and improve insulin sensitivity.

This mechanism is highly effective for many people, but not for everyone?

You hear? Not for everyone, and, not all the time…

Early research suggests that genetic differences could influence how individuals respond to GLP-1 and GIP-based medications.
Some key insights:

GLP1R Gene Variants: Differences in the GLP1R gene (which codes for the GLP-1 receptor) can affect how well people respond to GLP-1 agonists like Ozempic and Wegovy.

Appetite Regulation Genes: Variants in genes like MC4R and FTO, known to affect hunger and weight regulation, may also modulate how effective GLP-1 therapies are.

Metabolic Genes: Research into GIPR gene variations could shed light on why some individuals may respond especially well to dual-acting drugs like Zepbound.

A 2020 study published in Nature Communications highlighted how individual genetic profiles could impact the effectiveness of GLP-1 receptor agonists for weight loss and metabolic improvement.
Similarly, research from the University of Copenhagen showed that certain gene variants influence weight regain after stopping GLP-1 therapy, suggesting genetics matter for both immediate and long-term outcomes.

Why This Matters: The Dawn of Personalized Medication

For example, I have genes that make me more sensitive to medications, meaning, that in many cases, I need smaller doses. Should this mean I should be considered for tailored dosages for every medication I’m prescribed, based on my genetic profile? Or am I left with a constant trial-and-error process when it comes to finding the right treatment for me personally?

Personalized medicine based on genetic insights is what I look forward to.

A future where treatments are tailored to each individual, reducing guesswork and improving overall well-being.

Understanding how genetics interacts with medications like Ozempic, Wegovy, and Zepbound could unlock the future of truly personalized medicine.
Instead of a “one-size-fits-all” approach, we may soon predict:

  • Who will be “super-responders”
  • Who may require higher doses or different medications
  • How best to support long-term weight maintenance or other wanted effects.

As a nurse, I see huge potential in moving away from trial-and-error medicine to something more personalized, efficient, and humane for patients. Something other than standard SSRIs for everyone, -for everything.

This vision aligns beautifully with Scandinavia’s tradition of leading healthcare innovation — from our personalized cancer treatments to cutting-edge genomics research.

Scandinavian Innovation Beyond Ozempic

It’s not just Denmark making waves. Across Scandinavia, biotech and research communities are deeply involved in metabolic health and precision medicine:

Sweden: Karolinska Institutet researchers are exploring genetic predictors for obesity, diabetes treatment response, and metabolic disorders.

Norway: Scientists at the University of Oslo are studying how gut microbiome differences (partly genetically influenced) affect weight loss and medication response.

Finland: The groundbreaking FinnGen project is mapping how genetic variation influences everything from metabolism to cardiovascular risk -a treasure trove for future drug development.

There’s a growing belief here: Understanding individual biology will transform how we treat disease, not only in diabetes and obesity, but across all of medicine.

Looking Ahead: A Healthier, Smarter Future?

Do you have personal experience you’d like to share? Please do.

Ozempic, Wegovy, and Zepbound represent powerful tools.

-Well, they’re also a reminder: no medication is magic.
Our unique genetic makeup, lifestyle, environment, and social factors all weave together to determine outcomes.

Imagine a future where your DNA guides your treatment plan, helping you avoid unnecessary medications and giving you the best possible chance to thrive.

As a nurse, and as someone endlessly curious about human biology -I believe we are just at the beginning of this new era of precision health.
And seeing how Scandinavian research and innovation are helping to lead the way makes me incredibly hopeful, for all of us.

Written by Clara Vinter
Nurse, lifelong learner, and explorer of the intersections between genetics, innovation, and human health. claravinter.writer@gmail.com

Disclaimer:
This article is based on personal observations and publicly available research. It is for educational purposes only and is not intended as medical advice. I am not a medical doctor. Always consult a qualified healthcare provider before making any health decisions.

Ozempic

Wegovy

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The blog from Clara Vinter

Are You Fast (and Euphoric) Because of Your Genes?

Clara Vinter

5 min read

2025-04-23

 

by Clara Vinter writer

In my twenties, I loved running. I ran 3-4 times a week for about 15 years, and on top of that, I biked to and from work and picked up the kids from daycare.

 

-Not because I was training for a race, but because it became my regular routine. Running was something I could always do with ease, -just put on my shoes and head out the door.

There were days when the run felt light and effortless, as if my legs had their own rhythm. And then there were days when every step felt heavy. I often asked myself: is this just in my head, or is there something deeper? Something in my biology that affects how we move?

As a nurse, I’ve always been curious about the connection between the body and our lived experience. Over the past few years, my interest in genetics has grown, not just in terms of illness, but in everyday things, like why some people are naturally quick on their feet while others are steady and enduring.

A Closer Look at ACTN3

One gene that keeps coming up in the research is ACTN3. It influences the production of a protein found in fast-twitch muscle fibers, the type responsible for explosive power, like sprinting. Some people have a version of the gene (the R-variant) that helps their muscles work efficiently in short bursts. Others have a different version (the X-variant), which is associated with better endurance.

Neither version is “better,” but they do seem to set the stage for different kinds of physical strengths.

This may help explain why some of us felt at home on the school track while others preferred long walks or team sports, or why some runners lean toward marathons, while others excel at the 100 meters.

The Power of BDKRB2

Another fascinating gene is BDKRB2, which plays a role in controlling blood pressure and blood flow. This gene impacts how well your muscles can get oxygen during physical activity, influencing endurance.

Research has found that certain variations of this gene are linked to better aerobic capacity, meaning people with these variations may be able to run longer without tiring, or recover from strenuous activity more quickly. If you’ve ever found yourself wondering how some people can push through long workouts with ease, this gene could be one reason why.

MTHFR, -More Than Just Folate

MTHFR, a gene involved in the processing of folate and homocysteine, may not directly affect speed, but it has broader implications for physical health. Variants of this gene can impact how well your body manages inflammation and oxidative stress, both of which are key to muscle function and recovery. For those with certain MTHFR variations, the body may struggle more with these processes, potentially leading to quicker fatigue or longer recovery times after exercise. It’s a reminder that genetics plays a role in both how we perform and how we recover.

Nuance: The link between MTHFR variants and athletic performance is less direct than for ACTN3 or BDKRB2. Poor MTHFR function can affect overall health (e.g., cardiovascular health, fatigue), but its impact on muscle recovery or exercise performance is not as well-established. Lifestyle factors like diet (folate intake) and supplementation can mitigate effects.

The Euphoric Running Gene? DRD4

A year ago, I found something that made me laugh and think, “Is this me?!” There’s a gene called DRD4, associated with dopamine regulation, the neurotransmitter linked to reward and motivation. Some variations of this gene have been connected to increased feelings of excitement, reward, and even euphoria when engaging in physical activity. I couldn’t help but smile when I read about it. It made so much sense! I had always felt a kind of “euphoria” when I was running, -that burst of joy and energy that made the run feel almost effortless, like a natural high. I told my kids about it, and we had a good laugh, thinking that my ‘euphoric running’ was probably linked to this gene. Curious as ever, I looked into it more…-and sure enough, there it was: a genetic link to that feeling I’d always loved during my runs.

Nuance: While DRD4 may play a minor role in exercise reward, FAAH (anandamide regulation) and OPRM1 (endorphin signaling) are the most likely genes to influence euphoria during running, with DRD2, COMT, and SLC6A4 contributing to reward and mood. The runner’s high is a complex, multifactorial phenomenon, and no single gene fully accounts for it.

Beyond Speed: The Influence of COMT

Speed isn’t only about muscles; it’s also about your brain’s response to stress and effort. The COMT gene plays a role in the breakdown of dopamine, the neurotransmitter that affects mood and motivation. If you carry the Val variant of the gene, you might feel more driven, more focused during physical exertion, which could enhance performance in sports or challenging tasks. On the other hand, the Met variant might lead to quicker burnout under stress, which could influence how long you can sustain intense physical activity.

I’ll revisit this gene in a later blog post to dive deeper into its influence.

It’s Never Just One Gene

Of course, ACTN3, BDKRB2, MTHFR, DRD4, and COMT are just pieces of a much larger puzzle. Dozens of other genes influence things like your metabolism, muscle recovery, and how your brain processes physical effort. Your environment, your diet, stress levels, sleep patterns, and overall lifestyle -also shapes how your genetic traits come to life. It’s a complex, beautiful interaction between what’s in your DNA and what you experience in your daily life.

Genomic studies (e.g., Rankinen et al., 2016) estimate that over 200 genetic variants contribute to physical performance, with no single gene being dominant.

Knowing, Not Limiting

I don’t believe we should let our genes define us. But understanding them can help us shift from self-criticism to curiosity. Maybe you’re not slow, maybe you’re built for a different kind of strength. Maybe it’s not laziness or lack of effort, but a body that’s wired to perform in its own way, on its own timeline.

Looking back on those 15 years of running 3-4 times a week, I realize just how much I loved it. I wasn’t racing anyone, but I was racing my own body to see just what it was capable of. And even now, I’m still learning how to listen to what it’s saying. Maybe it’s time to start running again. Just for the joy of it, -and to see if that euphoric feeling comes back?

I´ll let you know. I sure will! 👟👟


Clara Vinter
Registered Nurse | Sweden
Writing about genes, the body, and the everyday science of being human

Disclaimer: I am not a doctor, and the information provided here is based on current research and my personal understanding. Gene research is advancing rapidly, and new findings may alter our understanding of genetic influences on health and performance. Always consult a healthcare professional for personalized medical advice or concerns regarding genetics, health conditions, or treatments.

The blog from Clara Vinter

The COMT Gene: How Your DNA Affects Stress, Focus, and Your Coffee Habit

Clara Vinter 2025-04-22

3 min read

By Clara Vinter

Welcome, and thank you for joining me!

Today, we’re talking about a gene that might explain why you handle stress differently than others and how it could even influence your relationship with coffee. That gene is COMT, or catechol-O-methyltransferase, and it plays a crucial role in how our bodies process dopamine 

-a neurotransmitter that affects our mood, focus, and energy.

What is COMT?

COMT is an enzyme that helps break down neurotransmitters like dopamine, epinephrine, and norepinephrine, chemicals that influence how we think, react, and feel. The speed at which this process occurs varies from person to person, which means some people experience stress more intensely, while others handle it with ease. The same goes for how we respond to stimulants like caffeine.

Here’s how your COMT type can impact you:

• Warrior (Val/Val): If you have this version of COMT, you break down dopamine quickly. You’re calm under pressure and tend to thrive in high-stress environments. But, you might struggle to stay focused when the pace slows down, and caffeine likely won’t affect you much, -you can handle multiple cups with no problem.

Example: Think of someone who can manage tight deadlines and chaotic situations without losing focus but finds it difficult to stay motivated with routine tasks. They likely don’t need coffee to power through their day.

• Worrier (Met/Met): If you have this version, you break down dopamine slowly. You might be more sensitive to stress and find it harder to bounce back from intense emotions. Caffeine can make you feel jittery or anxious, as your body processes it more slowly.

Example: You might feel mentally drained after a stressful day and prefer a quiet environment to recharge. A cup of coffee may make you feel anxious or over-stimulated, so you likely choose tea or avoid caffeine altogether.

• Balanced (Val/Met): If you fall into this category, you have a combination of the two. You can handle stress effectively, but you’re not immune to it. You likely enjoy coffee but don’t rely on it to get through your day.

Example: You’re able to manage your workload efficiently, with a good balance of energy and focus. A cup of coffee can help you stay alert without feeling overstimulated.

Why Does It Matter?

Understanding your COMT type can provide valuable insights into how your body responds to stress, focus, and caffeine. If you’re someone who feels easily overwhelmed by stress or finds that caffeine affects you strongly, knowing your COMT type can help explain why. It can also guide you in making better choices about your daily habits, from how you manage your workload to how you fuel your body.

My Personal Connection to COMT

As a nurse with 20 years of experience, I’ve seen firsthand how important it is to understand the role our genes play in our health. Personally, learning about my own COMT type helped me better understand why I react the way I do to stress and why certain habits, like caffeine consumption, impact me.

Like the Vikings, I carry this strength in my genes! This gave ”Vikings” a whole new angle!

The Power of Knowing

Your COMT type is just one part of the puzzle, but it can provide helpful insights into your unique stress-response system. Understanding how your body processes dopamine can help you adjust your daily routine and optimize your well-being.

In future posts, I’ll continue exploring the connection between our genes, daily habits, and health. Your genetics play a big part in shaping your health.

Thank you for reading, and I look forward to sharing more with you in the weeks ahead.

With warmth,

Clara Vinter, Viking by genes

Please note, this is not medical advice, but rather an exploration of how genetics can influence our health and well-being.

Connect: claravinter.writer@gmail.com

 

Gene, Genehealth, Wellness Tips, WellnessJourney , DNA

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