Thesis related to LSJL

APPLICATION OF QUANTITATIVE ANALYSIS IN TREATMENT OF OSTEOPOROSIS AND OSTEOARTHRITIS

“The math model of osteoporosis reveals a quick response to salubrinal and a delayed
but substantial response to knee loading”<-knee loading=LSJL

“the epiphyses of the proximal tibia and the distal femur are loaded, increasing intramedullary pressure in the adjacent bones. This pressure leads to interstitial fluid flow, which has been
shown to induce bone formation”<-interesting that the intramedullary pressure leads to the fluid flow and dismissing possible effects of the pressure itself.

Osteoperosis study:

C57BL/6 female mice (8 weeks old) were housed four to five mice per cage at the
Indiana University Animal Care Facility and fed with mouse chow and water ad
libitum.

“Loads were applied in the lateral-medial direction for 3 minutes/day at 15Hz, with peak-topeak
force of 0.5 N.”

“knee loading and salubrinal application elevated BMD via sclerostin and phosphorylated eIF2❛ (p-eIF2❛), respectively”

“Under 4-week salubrinal application, the BMD of ovariectomized mice decreased only 13%, with osteoblast activity increasing 136% while osteoclast activity decreased by 48%. After 4 weeks of knee loading, the BMD of ovariectomized mice decreased only 12%, with osteoblast
activity increasing 136% osteoclast decreasing 34%”

” loading’s suppression of p-eIF2❛ did not propagate to ATF4 and NFATc1.”

“ATF4 was modeled to increase the differentiation rate of osteoblast  precursors to active osteoblasts, while NFATc1 was modeled to increase the production of osteoclast precursors.”

” Loading was found to be more effective when applied earlier, as its effects are long term. Salubrinal seems to have a more immediate effect, thus being more advantageous when applied closer to the data collection time.”

Review Of Orthopaedic Surgeon Dr. Dror Paley

1. Dror Paley, MD, FRCSC, Medical Director at Paley Advanced Limb Lengthening Institute, Advanced Orthopedic Institute at St. Mary’s Medical Center

Description: Board-certified, fellowship-trained orthopedic surgeon and is nationally and internationally recognized for his expertise in deformity correction and limb lengthening. (Note: I highly recommend Dr. Paley for his credentials, exposure, and experience.)

901 45th Street – Kimmel Building
West Palm Beach, FL 33407
877-765-4637 (Toll Free)
Office – (561) 844-5255   Fax – (561) 844-5245
Email address: dpaley@lengthening.us

Website: Paley Institute

Wikipedia Article About Dr. Paley

My Review: There is not doubt and question that Dr. Paley is a world expert at his chosen field of Practice. He has developed some revolutionary surgical techniques for limb deformity treatment and if you were to desire to gain extra height, Dr. Paley is the person to do it. However, it seems that he is a little bit inattentive, hard to reach, and doesn’t focus much of his time on connecting to the patient. That is understandable given his schedule and his work. Some things that were brought up in the reviews is that it seems Paley may be involved in some immoral medical practices in getting cheaper rates for external fixators. I don’t know anything about this claim.

From Vitals.com 

Dr. Dror Paley, MD is a male with 29 years of medical experience and practices in Orthopaedic Surgery.

Saint Mary’s Medical Center

901 45th St
West Palm Beach, FL

See all of Dr. Paley’s practice locations

Hospital affiliation
Hospital affiliation

 Patient Ratings & Comments
The Overall Average Patient Rating of Dr. Dror Paley, MD when asked is Good.
Dr. Paley has been reviewed by 17 patients. The rating is 3.0 out of 4 stars. Read Reviews
Insurance

Dr. Paley accepts the following insurance plans:

  • 17 United Healthcare Plans
  • 6 Cigna Plans
  • 1 ODS Health Plan
  • 1 USA H & W Network Plan
  • 6 CareFirst Plans
  • 1 United Health Group, Inc. – Americhoice Plan
  • 2 Priority Partners Plans

See additional insurance networks and plans that are accepted.

Need health insurance? It’s more affordable than you think! Get an INSTANT quote!

Education Summary
Dr. Paley graduated from University Of Toronto Faculty Of Medicine.
Learn more about Dr. Paley’s medical training.
Hospital Affiliation
See all hospital affiliations.
Publications
Review specific publication excerpts.
Awards & Distinctions

America’s Leading Experts recognizes the top 15% of physicians who are proficient publishers on a specific disease, disorder or medical condition. Dr. Paley of West Palm Beach, FL recognition highlights his research proficiency in Orthopaedic Surgery.

Castle Connolly Top Doctors™ are specialists and primary care physicians who are highly recommended by their peers and other healthcare professionals. This recognition identifies the top physicians who possess a high level of medical skill and expertise. Dr. Paley of West Palm Beach, FL has been recognized in 2012, 2011, 2010, 2009.

Read more about other awards, appointments and associations.

Board Certification, Specialty and Expertise

Dr. Dror Paley, MD has obtained board certification from the member board for Orthopaedic Surgery.

In addition to the specialty of Orthopaedic Surgery, Dr. Dror Paley, MD has expertise in 21 areas. This includes Pediatric Orthopaedic Surgery, Acquired Joint Deformities, Broken Bones Bone Fractures plus others.
View ABMS Certification

Licenses
A medical license is required for a doctor to receive a NPI number and practice in any given state. Requirements vary by state but most require, at a minimum, post-graduate training in the doctor’s specific specialty. Dr. Dror Paley is confirmed to have a license in FL and MD.
Where does Dr. Dror Frcsc Paley practice?
Dr. Dror Paley practices Orthopaedic Surgery near West Palm Beach, FL.
Additional practice locations include: Baltimore, MD
See other West Palm Beach Surgeons and West Palm Beach Orthopedic Surgeons.

Overall Patient Rating    

Based on 17 ratings (see all)

Overall Rating

The Overall Average Patient Rating of Dr. Dror Paley, MD is Good. Dr. Paley has been reviewed by 17 patients. The rating is 3.0 out of 4 stars.

Wait Time
The average wait time to see Dr. Paley according to patient reviews, is 55 minutes. By comparison, patients wait a national average of 21 minutes before seeing a doctor.

Patient Ratings
Dr. Paley is rated “GOOD” in the following areas:

Ease of Appointment — 3.1
Courteous Staff — 2.6
Accurate Diagnosis — 2.9
Bedside Manner — 2.5
Spends Time with Me — 2.5
Follow Up — 2.5

Dr. Paley is rated “FAIR” in the following areas:

Promptness — 1.8

From RateMDs.com

Dr. Dror Paley
Doctor
  • Location:
  • WEST PALM BEACH, FL
  • Gender:
  • M
  • Specialty:
  • Orthopedic Surgeon
  • Webpage:
  • lifebridgehealth.or… External Link
  • Practice:
  • Hospital:
  • Sinai Hospital Of Baltimore
  • Answers Email:
  • N
  • Online Appt. Scheduling:
  • N
  • Accepting New Patients:
  • Y
  • Phone:
  • 410-601-4200
  • Med. School:
  • Grad. Year:
  • 1979
Rating: 3.9 out of 5, based on 6 reviews.
Dr. Paley has a good overall rating, based on 6 helpfulness and knowledge ratings of this doctor.
Date Staff Punctual Helpful Knowledge Comments
1649251
Click to report rating
12/1/11 1 1 1 1 Does anyone realize Dr. Paley, was dismissed from his hospital that he was practicing in while in Maryland. He was fee splitting money from the representive who was supplying the frames he uses at the hospital. Plus, the representive was his girlfriend. Needless to say, he was dismissed from the hospital he was at. Read the responses to this rating
1508235
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8/9/11 5 2 5 5 Although you may have to wait for Dr. Paley for hours, it is well worth it. He doesn’t send anyone home without seeing you and has been in the office as late as 10:30 pm to ensure that everyone is seen. My son broke his leg last week and his PA sent him the xrays via email on his Iphone and Dr. Paley responded within minutes all the way from Sicily. How many doctors would do that? Dr. Paley is the best surgeon and is the only surgeon I would trust to operate on my son’s deformities (TAR Syndrome). I can’t say enough great things about him and his entire staff.
Insurance: Aetna
Logged in users can respond to this rating
1194037
Click to report rating
6/22/10 5 3 5 5 Dr. Paley is unquestionably the most competent orthopedic surgeon in the US, and possibly the world in the field of leg lenghtening and handling complex orthopedic cases, particularly pediatric. My 14 year old son has had 16 surgeries, 3 with Dr. Paley, and is nw walking with a kneed that bends after 4 prior surgeons recommended amputation or fusion. To be treated by the best surgeon to receive the gift of mobility and limb functionality is worth every hour of waiting time.
Insurance: Blue Cross / Blue Shield
Logged in users can respond to this rating
1160573
Click to report rating
4/30/10 1 1 2 5 Dr. Paley made me feel like I did not matter. At all. I never saw him post-op, and whenever I had problems with my fixator (such as a strut popping off!) I could not reach him for several days. To me, even if this was a matter of personality conflict, it was extremely unprofessional and really cost me in terms of fighting spirit. After all, if the doctor isn’t behind you, who is? In my case, everyone else, I guess. I wouldn’t go back to the office. Logged in users can respond to this rating
45346
Click to report rating
9/14/06 2 5 5 He may be overbooked and time delayed, but he is the most incredible doctor I have ever known. He is the #1 doctor in the nation and internationally for limb deformity. He saved my leg when 3 other orthopaedic doctors wanted to amputate. I walk today unassisted,on my own two feet. The time I have had to wait was a small price to pay to have both of my legs and feet. As for bedside manner, he is honest, caring, and to the point. You may have to wait to see him, but the rewards are priceless. He never has short changed me on time, or attention to my medical needs when I am in his office. He gives everyone the time necessary to treat, answer questions, and provide what is needed for each patient. Logged in users can respond to this rating
42531
Click to report rating
8/26/06 1 3 5 Dr. Paley is technically the best in his field. I trust hom completely in terms of medical decisions. Unfortunatley he is so busy that you must often wait hours – 3-5 hours – to see him past your scheduled appointment. His bedside manner is also rather lacking. Unless you have a specific questions ready to ask him he will be in and out of the room in a matter of minutes.

Review Of Orthopaedic Surgeon Dr. Amar Sarin

2. Dr. Amar Sarin, Orthopaedic Consultant and Restorative Surgeon

Description: Dr. Sarin has worked at Institute for Invalids & Reconstructive Surgeries Ukraine Region, Vinnitssa Medical Institute Hospital Vinnitssa U.S.S.R. for Reconstructive Surgeries, Rehabilitative Surgeries and Illizarov Technique of Bone remodeling. In 20 years he has performed more than 3000 Ilizarov surgeries.

Website: Dr. Amar Sarin, Orthopaedic Consultant and Restorative Surgeon 

Address: Clinic Address: A-136, Super Mart 1 , DLF Phase 4, Gurgaon, India

Practice Location: B L Kapur Mqemorial Hospital, Action Cancer Institute, Nova Surgical Center

My Review: There is a major problem in reviewing Dr. Sarin and it is because he is based in New Delhi, India. If he was based in the US there would be at least 4-5 medical database resources where previous patients have been able to give their opinions and reviews on him. However his New Delhi clinic seems to mean that few of his patients have been able to post their reviews online. From his profile on his website, I would say that he is credible and if you could only get surgery in India without leaving the country, then Dr. Sarin would be an appropriate choice. I had expected that he would be located in the USA with many reviews but there seems to be none at all, at least that I have found. 

There is one post on the Make Me Taller forums HERE which criticizes the Dr. but most people on the forums trust the doctor in his abilities. 

There is one main review of Dr. Sarin from the Grow Taller forums HERE and the person who met him seems to have mostly a positive experience with him. I would recommend Dr. Sarin but any patient should still always do their research to make sure that the person who is about to operate on them has the skills and credibility. From the forums, the cost was approximately this for about 8 cm of height increase through tibia lengthening. 

Cost break down:Surgery:  $10,000
Stay:  $1000 per month (inclusive of food, medications, etc.)
Plane tickets:  $1200 two way (600 per trip).  Studentuniverse.com     has the cheapest flights to India but idk if you need to be a student per se.
Emergency cash: ~ $500.


From his website HERE.

Surgeon’s Profile of :

Dr. Amar Sarin joined as senior consultant at B L Kapur Hospital a Super Specialty Hospital 2 years back. Prior to this Dr. Sarin was associated with Action Medical Institute and was instrumental in creating the department of Illizarov surgery at Jaipur Golden Hospital served a period of seven years with the institute, steering it to newer milestones.

Dr. Sarin has a vast experience of doing advanced Illizarov procedures. He has performed advanced Illizarov over more than 3000 patients in the past 20 years.

He has also trained surgeons from other countries in basic and advance Illizarov and Ortho-oncology surgeries.

Previous Appointment:

Jaipur Golden Hospital, New Delhi
Action Medical Institute, Paschim Vihar New Delhi

Educational Training:

Medical School
M S Ramaiah Medical college Bangalore
Vinitssa Medical Institute Ukraine U.S.S.R.

Basic Illizarov Training
Vinnitssa Medical Institute, Ukraine

Advanced Ilizarov Training
Institute for Invalids & Reconstructive Surgeries
Ukraine Region, Vinnitssa USSR

Memberships and Fellowships:

Indian Orthopaedic Association

Special Interests:

Revision Illizarov Surgeries
Designing custom made prosthesis
Height Gain Surgeries

Hobbies:

Off-road driving

An Immortal Animal Turritopsis Nutricula And How To Apply It For Height Increase

Maybe 2 years ago I came across an article that talked about the only creature that human scientists know that can actually reverse the senescence process. This animal is the Turritopsis nutricula, a type of Jellyfish.

The wikipedia article on the Nutricula HERE

Turritopsis nutricula, the immortal jellyfish, is a hydrozoan whose medusa, or jellyfish, form can revert to the polyp stage after becoming sexually mature. It is the only known case of a metazoan capable of reverting completely to a sexually immature, colonial stage after having reached sexual maturity as a solitary stage.[2][3] It does this through the cell development process of transdifferentiation. Cell transdifferentiation is when the jellyfish “alters the differentiated state of the cell and transforms it into a new cell”. In this process the medusa of the immortal jellyfish is transformed into the polyps of a new polyp colony. First, the umbrella reverts itself and then the tentacles and mesoglea get resorbed. The reverted medusa then attaches itself to the substrate by the end that had been at the opposite end of the umbrella and starts giving rise to new polyps to form the new colony. Theoretically, this process can go on indefinitely, effectively rendering the jellyfish biologically immortal,[3][4] although in nature, mostTurritopsis, like other medusae, are likely to succumb to predation or disease in the plankton stage, without reverting to the polyp form.[5] No single specimen has been observed for any extended period, so it is not currently possible to estimate the age of an individual, and so even if this species has the potential for immortality, there is no laboratory evidence of many generations surviving from any individual.

The medusa of Turritopsis nutricula is bell-shaped, with a maximum diameter of about 4.5 millimetres (0.18 in) and is about as tall as it is wide.[6][7] The jelly in the walls of the bell is uniformly thin, except for some thickening at the apex. The relatively large stomach is bright red and has a cruciform shape in cross section. Young specimens 1 mm in diameter have only eight tentacles evenly spaced out along the edge, while adult specimens have 80-90 tentacles. The medusa (jellyfish) is free-living in the plankton.[edit]Description

Turritopsis nutricula also has a bottom-living polyp form, or hydroid, which consists of stolons that run along the substrate, and upright branches with feeding polyps that can produce medusa buds.[8] These polyps develop over a few days into tiny 1 mm medusae, which are liberated and swim free from the parent hydroid colony.

Images of both the medusa and polyp of the closely related species Turritopsis rubra from New Zealand can be found online.[9] Until a recent genetic study, it was thought that Turritopsis rubra and Turritopsis nutricula were the same. It is not known whether or not T. rubra medusae can also transform back into polyps.

Distribution and range

Turritopsis is believed to have originated in the Caribbean but has spread all over the world, and has speciated into several populations that are easy to distinguish morphologically, but whose species distinctions have recently been verified by a study and comparison of mitochondrial ribosomal gene sequences. Turritopsis are found in temperate to tropical regions in all of the world’s oceans.Turritopsis is believed to be spreading across the world as ships are discharging ballast water in ports. Since the species is immortal, the number of individuals could be rising fast. “We are looking at a worldwide silent invasion” said Smithsonian Tropical Marine Institute scientist Dr. Maria Pia Miglietta.

Life cycle

The eggs develop in gonads of female medusae, which are located in the walls of the manubrium (stomach). Mature eggs are presumably spawned and fertilized in the sea by sperm produced and released by male medusae, as is the case for most hydromedusae, although the related species Turritopsis rubra seems to retain fertilized eggs until the planula stage.[9] Fertilized eggs develop into planula larvae, which settle onto the sea floor (or even the rich marine communities that live on floating docks), and develop into polyp colonies (hydroids). The hydroids bud new jellyfishes, which are released at about 1 mm in size and then grow and feed in the plankton, becoming sexually mature after a few weeks (the exact duration depends on the ocean temperature; at 20 °C (68 °F) it is 25 to 30 days and at 22 °C (72 °F) it is 18 to 22 days).[3]

Biological immortality

Most jellyfish species have a relatively fixed life span, which varies by species from hours to many months (long-lived mature jellyfish spawn every day or night; the time is also fairly fixed and species-specific). The medusa of Turritopsis nutricula is the only form known to have developed the ability to return to a polyp state, by a specific transformation process that requires the presence of certain cell types (tissue from both the jellyfish bell surface and the circulatory canal system). Careful laboratory experiments have revealed that all stages of the medusae, from newly released to fully mature individuals, can transform back into polyps. The transforming medusa is characterized first by deterioration of the bell and tentacles, with subsequent growth of a perisarc sheet and stolons, and finally feeding polyps. Polyps further multiply by growing additional stolons, branches and then polyps, to form colonial hydroids. This ability to reverse the life cycle (in response to adverse conditions) is probably unique in the animal kingdom, and allows the jellyfish to bypass death, rendering Turritopsis nutricula potentially biologically immortal. Studies in the laboratory showed that 100% of specimens could revert to the polyp stage, but so far the process has not been observed in nature, in part because the process is quite rapid and field observations at the right moment in time are unlikely. In spite of this remarkable ability, mostTurritopsis medusae are likely to fall victim to the general hazards of life as plankton, including being eaten by other animals, or succumbing to disease.

Benefits for humans

The Turritopsis nutricula’s cell development method of transdifferentiation has inspired scientists to find a way to make stem cells use this process for renewing damaged or dead tissue in humans.

From Discovery News website …

‘IMMORTAL’ ANIMALS REVEAL ANTI-AGING SECRETS

Analysis by Jennifer Viegas 
Thu Apr 21, 2011 12:56 PM ET 

Some animals and plants that reproduce asexually “can in principle achieve essentially eternal life,” according to a University of Gothenburg press release.

Scientists at the university are studying such species to find out how they avoid aging. So far, one chemical appears to be key: telomerase. This is an enzyme that protects DNA. It is more active in the longest-lived people, so its benefits likely extend throughout the animal kingdom.

The animals that can possibly achieve immortality under ideal conditions, such as sea squirts, certain corals, Hydra, and Turritopsis nutricula (the immortal jellyfish), often activate telomerase. Helen Nilsson Sköld of the Department of Marine Ecology, University of Gothenburg, and colleague Matthias Obst are studying sea squirts and starfish to learn more about how these marine creatures seem to ward off aging.

Out of the animal immortality A-list, sea squirts and starfish have genes that most closely resemble those of humans.

“Animals that clone themselves, in which part of an individual’s body is passed on to the next generations, have particularly interesting conditions related to remaining in good health to persist,” Sköld was quoted as saying in the press release. “This makes it useful to study these animals in order to understand mechanisms of aging in humans.”

“My research has shown that sea squirts rejuvenate themselves by activating the enzyme telomerase, and in this way extending their chromosomes and protecting their DNA,” she added. “They also have a special ability to discard ‘junk’ from their cells. Older parts of the animal are quite simply broken down, and are then partially recycled when new and healthy parts grow out from the adult bodies.”

Starfish are also amazingly immune to problems that affect the rest of us. If they lose a body part, for example, many species can simply grow another one. Reproduction involves tearing apart their bodies, somewhat akin to growing a new plant from a broken off piece of a “mother plant.”

Eternal life, from an evolutionary standpoint, however, has a big drawback. Due to asexual reproduction, the species as a whole retains very low genetic variation. This means they could be particularly vulnerable to climate change and not enjoy immortality after all.

Scientists are therefore rushing to study such species, which may hold the secrets of increasing our own longevity. It would be a colossal human mistake if our pollution, habitat encroachment and other activities erased our chances of learning more about nature’s anti-aging secrets.

Me: This is what the scientists are saying about it’s age reversing powers…”undergo a sort of reverse metamorphosis back to its youthful form as a stalk-like polyp” and “infinite do-overs is a process called transdifferentiation, which turns one type of cell into another. While other animals can undergo limited transdifferentiation to regenerate organs (salamandars can regrow limbs, for example), Turritopsi is the only one that can regenerate its entire body.”

From this scientific article from Science Pub HERE

Transdifferentiation occurs when a non-stem cell turns itself into another type of cell. But, it is not clear if stem cells are involved in this immortality or not. As my opinion, the transdifferentiation in Turritopsis nutricula has related mechanism to stem cell when the life cycle reverted. It is important to reveal the relationship of this Turritopsis nutricula transdifferentiation and stem cell. Transdifferentiation is rare, and when it does occur, it most commonly occurs in parts of the organsism, like in the eye of the salamander. However, the immortal jellyfish has incorporated transdifferentiation into its lifecycle. In the process, all of the old cells are regenerated. At the end of the cycle, the immortal jellyfish is a young polyp, ready to start life anew (Wendy, 2009). 

In the laboratory, 100% of these medusae regularly undergo this change. The cells that accomplish the building of a new stolon are probably those of the exumbrella. However, it is not known whether the sensory cells, myoepithelial cells, and cnidocytes are derived from the exumbrella or the endodermal component. 

Germline stem cell is the cell in the earliest of the cell stage. It is possible to inject the germline stem cell into adult human body to get the eternal life (Ma Hongbao 2007). However, the reveal of the transdifferentiation mechanism of the jellyfish Turritopsis nutricula will offer the chance to explore the possibility of the eternal life for human. 

This is done through a cell change in the external screen, exumbrella. In it’s life cycle, the medusa is transformed into a stolon and the polyps into a hydroid colony. The umbrella turns inside out; middle section and tentacles are reabsorbed before the polyp spawns. Stolons form two days before the polyps differentiate. 

It can do this because it can alter the differentiated state of a cell, transforming it into another cell type, called transdifferentiation, and it is usually seen only when parts of an organ regenerate. 

In this transdifferentiation process, the medusa is transformed into the stolons and polyps of a hydroid colony. First, the umbrella everts and the tentacles and mesoglea are resorbed. The everted medusa attach to the substrate by the end that had been at the opposite end of the umbrella, and spawning occurs shortly thereafter. The cnidarian then secretes a perisarc and stolons. Two days after the stolons are first seen, polyps differentiate. 

Conclusion: For this article post, I wanted to state first that I want to leave all of the talk for the application of human immortality possibilities to other scientists but I wanted to focus on the possibility of using the ability of the Nutricula on height increase. If we can figure out the entire mechanism of transdifferentiation, I would be willing to bet that we can figure out the trigger signals that cause the cells to change into the type that we desire. 

Theoretically, if we can get the right signals triggered, we can get the obsteoblasts and even the osteoclasts in the human bone which are live organisms to revert back into chondrocytes, original mesenchynaml stem cells, and cartilage cells. If we can get the bones cells to use transdifferentiation to revert to cartilage cells, get others to turn into chondrocytes, and get another layer of bone cells into stem cells, we can create growth plate cartilage in places in our body again, and that would lead to natural height increase as before. The hard cortical bone matrix made of collagen and calcium and mineral deposits can be reabsorbed into the body and it is replaced by the cartilage.  

 

The Connection Between Testosterone, Male Penis Size, And Finger Length Ratio

For any of us who has ever taken a college biology course, we might remember the professor stating the study that showed that men who have more testosterone in their bodies have longer ring fingers than their index fingers, relative to the longest finger which is the middle finger.

Well another study came out recently that showed a correlation between the size of the male penis and the person’s finger length ratio, specifically the ringer finger to the index finger. This type of study can be connected to the previous study about testosterone link to ring finger length.

Obviously longer ring finger length, means greater finger ratios, assuming the index finger is kepted constant and don’t change from an increase in testosterone. The would suggest that an increase in the testosterone in a male’s body would increase the size of the male penis.

The study was reported in the Summer of 2011 and ABC News and CBS News (as well as dozens of other news stations) picked up the story. The article is posted below (source HERE).


Penis size linked to finger measurements, say Korean scientists

(CBS) – Despite the rumors, shoe size and hand size won’t predict a man’s size…down there. What can? Researchers at Gachon University in Incheon, South Korea think they’ve found the answer.

They say two fingers can tell the whole tale.

For the study, published in the Asian Journal of Andrology, researchers looked at the relationship between the size of the second digit, or index finger, and that of the fourth digit, the ring finger – in 144 Korean men aged 20 or older. All these men were in the hospital undergoing urological surgery for conditions unrelated to penis length.

After measuring pre-and post-surgery lengths for all three “digits,” the researchers found the average length between the second and fourth finger was 0.38 inches, and ranged from 0.35 to 0.44 inches, according to LiveScience. These measurements may be too small for the naked eye to notice, but when the researchers compared these finger lengths with penis size, they found the lower the digit ratio, the longer the penis was.

What does that mean?

“According to our data…the shorter index finger than ring finger you have, the longer stretched penile length you have,” Dr. Tae Beom Kim, study author and professor of urology at Gachon University in Incheon, South Korea, told Reuters.

Put your hands down, fellas. These findings may serve as fraternity fodder, but what are the medical implications of studying digit size?

Several studies have linked the distance between the second and fourth finger to sperm count and heart attack risk, LiveScience reported. But finger size has also been linked to other deadly diseases.

Dr. Denise Brooks McQuade, professor of biology at Skidmore College in N.Y, wrote in an accompanying commentary to the study, that digit ratio can help doctors gauge how much testosterone a fetus is exposed to in the womb, which has been linked to an increased risk for hormone-driven diseases like prostate cancer.

She points to a 2011 study that found participants that had an “index finger longer than ring finger were significantly less likely to have prostate cancer.” The authors of that study said a high digit ratio might display a protective benefit these patients have against the disease, according to her commentary.

“Digit ratio is non-invasive and easy to measure, yet may provide clues about an individual’s prenatal history.” McQuade told Reuters. “Combined with other information, digit ratio offers the potential for clinical usefulness.”

Maybe size does matter.

Conclusion: The extra testosterone level is stated to be from the womb that the male was in before birth. When we try to somehow use this type of study for our height increase endeavors, we could make the theory that men who have more testosterone are more likely to exhibit alpha male behavior. If they are more likely to exhibit alpha male behavior, I would guess they are more likely to be taller and bigger than average, There have been already studies that disproved the myth of the Napoleon Complex which showed that taller males are more likely to exhibit dominating and violent tendencies than shorter onces, obviously with a clear correlation to testosterone levels. 

The conclusion I am willing to postulate at is that women who have more testosterone in their systems which reach their male offspring result in the male offspring in being slightly taller than their peers. We know that testosterone in females is linked to slightly stronger sexual drive. This could mean that females who have stronger sexual drives prefer at a instinctual level to mate with taller, more evolutionarily fit men than other women which have lower testosterone levels, who prefer less dominant, alpha male behavior males. 

This could imply that if one desired to have taller and bigger children, it may be better to have a higher testosterone level, whether naturally or through lifestyle changes. 

The Connection Between Noggin Glycoprotein And Height

This will be one of the shorter posts.

It is almost been completely concluded that the glycoprotein Noggin and the gene that creates inhibits longitudinal growth. Mutations in the gene often leads to tall stature.

from the wikipedia article on Noggin (HERE)

Noggin, also known as NOG, is a protein which in humans is encoded by the NOG gene.[1]

Noggin inhibits TGF-β signal transduction by binding to TGF-β family ligands and preventing them from binding to their corresponding receptors. Noggin plays a key role in neural induction by inhibiting BMP4, along with other TGF-β signaling inhibitors such as chordin and follistatin. Mouse knockout experiments have demonstrated that noggin also plays a crucial role in bone development, joint formation, and neural tube fusion

Molecular biology

The secreted polypeptide noggin, encoded by the NOG gene, binds and inactivates members of the transforming growth factor-beta (TGF-beta) superfamily signaling proteins, such as bone morphogenetic protein-4 (BMP4). By diffusing through extracellular matrices more efficiently than members of the TGF-beta superfamily, noggin may have a principal role in creating morphogenic gradients. Noggin appears to have pleiotropic effect, both early in development as well as in later stages. The results of the mouse knockout of noggin suggest that it is involved in numerous developmental processes, such as neural tube fusion and joint formation.

From HeightQuest they also mention that Noggin inhibits the affects of BMPs HERE

From this study HERE

Horm Res. 2008;69(4):221-6. Epub 2008 Jan 21.

Growth and skeletal development in families with NOGGIN gene mutations.

Oxley CD, Rashid R, Goudie DR, Stranks G, Baty DU, Lam W, Kelnar CJ, Ahmed SF.

Source

Department of Paediatric Endocrinology, Royal Hospital for Sick Children, Edinburgh, UK.

Abstract

INTRODUCTION:

There is a scarcity of data on height as well as bone densitometry in humans with NOGGIN mutations.

METHODS:

In 2 families with symphalangism, anthropometry, bone densitometry and genetic analysis of the NOGGIN gene were performed.

RESULTS:

In family A, the height standard deviation scores of the affected father and son were -0.4 and 3.5, respectively. In family B, the height standard deviation scores of the affected father, twin daughters and another daughter were 1.7, 1.8, 2.4 and 1.8, respectively. In the children, percentage predicted bone mineral content (BMC) for height at the appendicular sites (total femur, femoral neck) was lower than at an axial site lumbar spine. In the 2 fathers, median bone mineral density at total femur and femoral neck was -0.3 standard deviation scores (-0.7, 0.2) and at lumbar spine the scores were -0.4 and 0.9. The children had median tibial and radial speed of sound velocities of -2.1 (-0.9 to -6.4) and -1.4 (-0.2 to -4.9), respectively. DNA analysis revealed a novel missense mutation in family A and family B, resulting in a Met190Val substitution and a Pro42Arg substitution, respectively.

CONCLUSION:

Heterozygous gene mutations in NOGGIN are associated with tall stature in children but not necessarily in adults. The appendicular BMC and speed of sound may be low in affected children but normalises by adulthood. However, axial BMC seems normal in childhood and is high in adulthood.

(c) 2008 S. Karger AG, Basel

PMID: 18204269      [PubMed – indexed for MEDLINE]