Hair Loss InformationThe Hair on the Sides of My Head Started Thinning at 17 Years Old – Hair Loss Information – Balding Blog

Hello Dr. Rassman

I have a question about a condition I’ve had since the age of 17. During school i first noticed that the hair on the sides of my head started to thin, i then noticed general thinning of my entire scalp hair, i noticed the thinnest hair coming from the crown. as a few years pasted i noticed slight recession on both sides of my hairline.

What i find bizarre is that I’m now approaching 26 and still have pretty good coverage, the only thing I’ve noticed in the last 3 years is 2-3 tiny bald spots in random locations across the scalp (no conventional pattern) my crown thinning has not to my knowledge progressed

What i can tell you is that i am a male, my mother also has entire scalp thinning, but even thinner than mine but no slight recession. i always remember my mother having hair like this.

My father who’s 69 has still got quite a lot of hair, in fact he only started losing a bit of hair around his early 60’s.

If i do in fact have DUPA what does the future hold for me in terms of further hairloss?

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I do not know what you have, but if you have diffuse unpatterned alopecia (DUPA), then in the future you will have diffuse thinning in no particular pattern. I have no way to know how much more you will lose hair though, as everyone is different.

There is a cosmetic treatment for DUPA patients, called Scalp MicroPigmentation (SMP). It is not a cure by any means, but it can make you look fuller. In any event, you should see a doctor and get a diagnosis.

Hair Loss InformationStudy – Isolated Crown Balding and the Risk of Prostate Cancer – Hair Loss Information – Balding Blog

Snippet from the abstract:

Androgenetic alopecia (AGA) is a genetically determined skin condition strongly age dependent and androgens are assumed to play an important role in its development. A link between AGA and prostate cancer has been hypothesized because of their similar risk factors.

We sought to systematically review the evidence available on the association between AGA and risk of prostate cancer.

We searched the electronic databases MEDLINE and Cochrane for studies examining the association between AGA and risk of prostate cancer. We estimated pooled odds ratios (OR) and 95% confidence intervals. We also analyzed the OR for individual hair loss patterns, as defined by the Hamilton scale.

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Read the rest — Androgenetic alopecia and risk of prostate cancer: A systematic review and meta-analysis

Although many authors have investigated a possible association between androgenetic alopecia (AGA) and prostate cancer, there is not yet a definitive answer. Patients with any pattern genetic balding did not have an increased risk of prostate cancer, but patients with just vertex pattern AGA (crown balding without balding in other areas) had a significantly increased risk of prostate cancer versus control subjects. Vertex pattern AGA may be associated with an increased risk of prostate cancer.

In another publication, there was a higher risk of heart disease in patients with pure crown balding.

Erectile Dysfunction Can Possibly be Treated with Lifestyle Modifications – Hair Loss Information – Balding Blog

In the first journal of the International Society for Sexual Medicine, an article appeared titled, “The Incidence, Prevalence, and Natural History of Erectile Dysfunction“. The article (from Department of Urology, St. James University Hospital, Leeds, UK) covered some important points worth sharing with our readers:

1. “The varying methodologies, definitions, and populations make comparison difficult, but in high-quality studies there is a consistent association with age, and analytical studies suggest an association with cardiovascular risk factors, depression, and lower urinary tract symptoms. There is emerging evidence of a link with smoking and obesity.”

2. “Remission was commoner in younger men, suggesting that in these men psychological and lifestyle factors might be the cause of temporary self-limiting ED.”

3. “These studies also suggest that lifestyle modifications might be helpful in the prevention and treatment of ED.”

Read the full study abstract here.

I Was Diagnosed with Lichen Planopilaris – Hair Loss Information – Balding Blog

Hi,

I recently went to a dermatologist to be diagnosed with AGA despite no family history (even 3 generations back). I am a 29 year old male, who has been overweight for a few years (~50-60 lbs)and generalized anxiety disorder. I was prescribed “Valium” and a beta blocker called “Propranolol” in December 2009. Sometime in 2011, my head began to itch, sometimes more, sometimes less. By February 2012, I noticed suddenly that there was a thinning patch on my crown and my scalp looked red and inflamed and itched more often.

The dermatologist also took two 4 mm punch biopsies from two sites on my vertex and pathology sent them back as AGA w/ active “Lichen Planopilaris”! I had never even heard of this before. My research just shows me it’s extremely rare, is incurable and for the most part will ruin my life unless I enjoy being bald. What am I supposed to do? Everyone else is calm about the situation, and my derm says he doesn’t yet “buy it” that it’s lichen due to my clinical presentation (Are transverse biopsies ever wrong?)

I’ve read you can’t even restore your hair with HT if Lichen is there because it will just destroy that hair too. How does this Lichen disease come about? I’ve read beta blockers can cause lichen planus, and i’ve been on a low dose for 4-5 years now. I’m not sure what to do, I don’t know why I’d have LPP or where it came into existence from. If its me reacting to the drug, would my hair restore itself if I came off of it after years?

Does LPP also cause miniaturization of hairs because that’s apparently happening as well. How statistically unlucky does one have to be to have both AGA with no famiily history + some rare LPP disease that will scar my head for life?

I’m lost and confused and so far no one has begun any treatments for anything. I know I can’t take propecia, and I know steroids won’t be tolerated well in my body if I have this lichen disease of unknown origin.

Have I received a death sentence for my scalp? The crown/vertex is thinning and a small thinning keeps developing down the parting of my hair. My hairline itself hasn’t receded at all since puberty… The top of my scalp is generally pink/reddish at all times with a little red itchy bump scattered sporadically around my whole scalp.

Thank you for reading my desperate post. I’ve gone from the extremely thick course hair I’ve had my entire life and model with, to losing what feels like 70% of it in the course of 15 months at age 28-29. It is imperative that I restore my hair to its previous glory. I do have pictures if you are interested.

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Unfortunately, much of what you said is true. Transplanting hair into an area of active disease will kill the hair grafts. Most doctors will not do a surgery like a hair transplant where the odds are against the success of the procedure. I don’t know the specific statistics for those that have lichen planopilaris, as it is a rare scarring alopecia and difficult to treat.

There are some options: hair pieces, Scalp MicroPigmentation / SMP (which requires you to shave your head for best results), and topical concealers like Toppik.

Could the Atkins Diet or My Ankle Injury Have Caused My Rapid Hair Loss at 21 Years Old? – Balding Blog

I have really learned a lot reading your articles.

I am a 21 year old college student. About a year and a half ago I gained thirty pounds and in the last eight months lost 45 pounds, the bulk of which I lost the in the first four months through the Atkins Diet and intense working out. I also had a bad ankle sprain in the middle.

The past four months I have been experiencing shedding, rapid hair loss and a receding hairline. The front scalp has become very thin while the middle is still thick and grows normally. The right hairline has receded about one centimeter further than the left and I can also feel a bald spot, about the size of a nickel, on the right side of the back of my head. The scalp is very itchy and I find that after I itch that there is a white residue on my finger nails.

I feel like I am still young to have lost so much hair.

I still have relatively thick hair but it looks unnatural and frays to the left. Can this be tied to my weight loss, ankle injury or increased stress?

Acute weight loss can cause or accelerate hair loss. I would doubt your ankle injury had anything to do with your hair loss. It’s also possible that these things occurred coincidentally timed to your genetic predisposition.

As far as your nickle size bald spot at the back of your head, you need to see a doctor for this as there are many causes for such a problem. Without good pictures and an opportunity to examine you, there is little more I can say here.




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Balding Forum - Hair Loss Discussion

Temperament Change from Taking Propecia Reminds Me of Taking Antidepressants – Hair Loss Information – Balding Blog

I am now about five weeks into taking Propecia and think that it has affected my temperament. (It reminds me a bit of taking SSRI anti-depressants some time ago.) I little wish to lose my hair and will in a little while decide whether or not I continue with this medication which I gather takes about three months to have a noticeable effect.

What interests me is knowing whether or not this sex hormone pharmaceutical is more or less severe in its side-effects than the female contraceptive pill which it reminds me of (I am a medical layman) in its operation?

Hope that you do not mind a question from outside the United States!

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There are mental side effects reported in a small group of individuals, much as you described. I’ve written about this many times before, including here, here, and here.

In one study, finasteride has been found to inhibit hippocampal neurogenesis in mice, which is related to emotional behavior. There are reports in humans with the higher dose (5mg) used to treat the prostate, and Wikipedia lists a few very tiny studies from at least 6-10 years ago that might point to a link between depression and finasteride in humans. This preliminary study from nearly 7 years ago suggests that patients with a high risk of depression should be prescribed finasteride with caution.

A Few Hairs Are Weak and Wavy in My Otherwise Straight Hair – Hair Loss Information – Balding Blog

Hi,

I’ve noticed that a few of the hairs at my hairline have become ‘wavy’ where as most of my hairs stand straight. Is it the case that these hairs are miniaturising?

They don’t appear to be thinner in diameter than the hairs next to them…but also don’t seem to grow as strong (i.e. they ‘fall down’ rather than grow straight up).

Thanks in advance.

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The weaker hairs you’re seeing could be miniaturizing, or it could just be that you’re seeing hairs in different parts of the hair cycle. Without seeing you, I have no way to know.

If you want to know if you have started the balding process, looking at one hair at a time is not the way to go. See a doctor who will measure your hair bulk in different parts of the scalp. Balding people (even in the early part of the process where you can not see any thinning) will always show a reduction in hair bulk.

I Have Seborrhoeic Dermatitis, Chronic Telogen Effluvium, and Possibly MPB! – Hair Loss Information – Balding Blog

Hello,

I am 25 and have been gradually losing my hair for a couple for years now. In addition to what I would confidently call MPB, I also suffer from seborrhoeic dermatitis and chronic telogen effluvium.

1. Is the chronic TE linked to MPB or seb derm? I’ve suffered from TE for over a year and a half now and always assumed that losing hairs in this way was part of MPB. It constantly gets me down as I am constantly shedding hairs. A small pinch from anywhere from the top of my scalp can produce up to 20 plus hairs. It’s as if 50% of my hair isn’t even attached to my scalp. Several websites state that chronic TE is due to illness, whilst others say that it is the early stages of MPB.

2. Will the seb derm cause any hair loss if left untreated? Even though the seb derm is quite bad (thick yellow, oily scales all over my scalp), the condition is not yet visible to others and causes me no discomfort. I am worried about washing my hair every day with the recommended treatments because I lose so many hairs due to the TE.

Please help me! I’ve seen two doctors regarding my MPB and both told me that nothing could be done. I only discovered propecia etc. through google. I have been taking it for nearly 4 months now.

Many thanks for an enlightening website

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We are not, I suspect, one of the two doctors you have seen. I have no real experience in doing transplants on someone who has a pull test like you reported as evidence of chronic telogen effluvium. I am actually surprised that this has not come before me at an earlier time.

The seborrhea will not produce hair loss as long as you do not scratch or pick in involved areas. Transplants may be contra-indicated with a chronic telogen effluvium.

My Doctor Said I Wasn’t Programmed to Have Crown Loss, So Propecia Wasn’t Necessary – Hair Loss Information – Balding Blog

First, I can’t thank you enough for maintaining this resource–it’s alleviated a lot of my anxiety about hair loss simply by giving my a place to find answers to my questions.

I recently had a consultation with a surgeon about reshaping my temples. I’m 29, and probably a NW2-3. (I’ve had relatively high temples since high school, though the spaces have expanded slowly since though then.) He ultimately recommended 1100 grafts to fill in my temples and create a relatively straight hairline.

I have two questions:

1. He told me that diet has a significant impact on hair loss, second to genetics. He advised a vitamin regimen of L-Lysine, Vitamin E, Saw Palmetto, MSM, Glucosamine, Chondroitin Sulfate, and Ester-C. In addition, he recommended that I stop consuming creatine, and eat a sulphite/nitrite-free diet that’s rich in antioxidants and low in refined sugar and bleached flour. I realize that much of this might be good health advice generally, but does it have any non-negligible connection to hair loss? I appreciate interest in my general welfare, but this had me a tad skeptical.

2. After examining the entirety of my hair, he told me that I’m “programmed” for hair loss not beyond a NW3. He did not conduct a miniaturization study; this was a “naked eyeball” examination. Because he didn’t think I’m “programmed” for any crown-area loss, he said Propecia wouldn’t be necessary. Should I take this pronouncement with a grain of salt, or could he accurately reach that conclusion via the type of examination he made?

Many thanks, and all the best. If it’s at all relevant, he did not recommend any type of hairline lowering, but simply filling in the temples and leaving the forelock as is.

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While it is possible that you won’t advance beyond a Norwood class 3 hairline, I don’t trust doctors who give eyeball opinions for predicting hair loss. There are some good tests (miniaturization mapping and better yet, bulk analysis) that will tell you with some certainty if you are balding.

The decision to take drugs like finasteride should be based upon clinical evidence of balding. You might want to consider getting a second opinion, hopefully from a doctor that can give you a more thorough analysis of your hair. If you aren’t balding, Propecia isn’t necessary (though you should consider it to prevent shock loss from any hair transplant you may have). If you do have early balding, now would be the best time to start the medication.

As for the recommended vitamins, I am not a nutritionist, so your doctor’s suggestions may be good ones for your overall health. I wouldn’t expect to see lush hair growth upon taking them, though. None of those have satisfactory evidence linking them to treating genetic hair loss.