Library:Bone Density: First Do No Harm
A Ray Peat newsletter, 2006-08-13.
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No topic can be understood in isolation. People frequently ask me what they should do about their diagnosed osteoporosis/osteopenia, and when they mention “computer controlled” and “dual photon x-ray” bone density tests, my attention tends to jump past their bones, their diet, and their hormones, to the way they must perceive themselves and their place in the world. Are they aware that this is an x-ray that's powerful enough to differentiate very opaque bones from less opaque bones? The soft tissues aren't being studied, so they are allowed to be “overexposed” until they appear black on the film. If a thick area like the thigh or hip is to be measured, are they aware that the x-ray dose received at the surface where the radiation enters might be 20 times more intense than the radiation that reaches the film, and that the 90 or 95% of the missing energy has been absorbed by the person's cells? If I limited my response to answering the question they thought they had asked me, I would feel that I had joined a conspiracy against them. My answer has to assume that they are really asking about their health, rather than about a particular medical diagnosis.
Neurologists are famous for making exquisitely erudite diagnoses of problems that they can't do anything to remedy. The owners of expensive dual photon x-ray absorptiometer diagnostic machines are in a very different position. The remedies for osteoporosis are things that everyone should be doing, anyway, so diagnosis makes no difference in what the physician should recommend to the patient.
Most often, estrogen is prescribed for osteoporosis, and if the doctors didn't have their bone density tests, they would probably prescribe estrogen anyway, “to protect the heart,” or “to prevent Alzheimer's disease.” Since I have already written about estrogen and those problems, there's no need to say more about it here, except that estrogen is the cause of a variety of tissue atrophies, including the suppression of bone formation.[1]
General Electric, a major advocate of x-ray screening for osteoporosis and breast cancer, has advertised that 91% of breast cancers could be cured if everyone used their technology. Breast cancer has not decreased despite the massive application of the technology, though the U.S. government and others (using crudely deceptive statistics) claim that the War on Cancer is being won. Similarly, during the last decades when the “high technology” x-ray machines have been more widely used, the age-specific incidence of osteoporosis has increased tremendously. This apparently includes a higher rate of shortening of stature with aging than in earlier generations.[2]
I think there are several reasons for avoiding x-ray tests of bone density, besides the simple one that everyone should eat a bone-protective diet, regardless of the present density of their bones.
Even seemingly identical x-ray machines, or the same machine at a different time, can give very different estimates of bone density.[3][4][5][6][7][8][9][10] Radiologists evaluating the same images often reach very different conclusions.[11] Changes in the tissue water and fat content can make large differences in apparent bone density,[12] and estrogen, which affects those, could appear to cause improved bone density, when it is merely causing a generalized inflammatory condition, with edema. A machine that is accurate when measuring an aluminum model, won't necessarily give meaningful results when the composition of the tissue, including the bone marrow, has changed. Calcification of soft tissues can create the impression of increased bone density.[13] Studies of large groups of people show such small annual losses of bone density (around 1%), especially in the neck of the femur (which is important in hip fractures) that the common technical errors of measurement in an individual seem very large.- Ultrasound devices can do an extremely good job of evaluating both bone density and strength,[14][15][16] rather than just density.- Ultrasound stimulates bone repair.- X-rays accelerate the rate of bone loss.- X-rays do their harm at any dose; there is no threshold at which the harm begins.
X-ray damage is not limited to the area being investigated. Deflected x-rays affect adjacent areas, and toxins produced by irradiated cells travel in the bloodstream, causing systemic effects. Dental x-rays cause thyroid cancer and eye cancer. Recent experiments have shown that low doses of radiation cause delayed death of brain cells. The action of x-rays produces tissue inflammation, and diseases as different as Alzheimer's disease and heart disease result from prolonged inflammatory processes.
I have never known a physician who knew, or cared, what dose of radiation his patients were receiving. I have never known a patient who could get that information from their doctors.
The radiation exposure used to measure bone density may be higher (especially when the thigh and hip are x-rayed) than the exposure in dental x-rays, but dental x-rays are known to increase the incidence of cancer. Often, dentists have their receptionists do the x-rays, which probably doesn't matter, since the dentist is usually no more concerned than the receptionist about understanding, and minimizing, the dose. Even radiological specialists seldom are interested in the doses they use diagnostically.
It was only after a multitude of dentists had a finger amputated that it became standard practice to ask the patient to hold the film, while the dentist stood safely back away from the rays.
Just after the beginning of the century, Thomas Edison was helping to popularize x-rays, but the horrible death of his chief technician turned Edison into an enemy of the technology. By the 1940s, the dangers of radiation were coming to be understood by the general public, and it was only the intervention of the U.S. government, to popularize atomic bombs and nuclear power, that was able to reverse the trend.
In 1956 and 1957, Linus Pauling was the only well known scientist who opposed the government's policies. The government took away his passport, and his opportunities to write and speak were limited by a boycott imposed by a variety of institutions, but instigated by the nuclear industry and its agent, the Atomic Energy Commission. The government which considered Pauling a threat to national security, had placed thousands of German and Hungarian “ex”-Nazis in high positions in industry and government agencies, after protecting them from prosecution as war criminals. The official government policy, directed by the financier Admiral Strauss who controlled the Atomic Energy Commission, was to tell the public that radiation was good. Their extreme secrecy regarding their radiation experiments on Americans, however, indicated that they were aware of the malignant nature of their activities; many of the records were simply destroyed, so that no one could ever know what had been done. Scientists who worked for the government, Willard Libby, John Goffman, and many others, were working to convince the public that they shouldn't worry. Of the multitude of scientists who served the government during that time, only a few ever came to oppose those policies, and those who did were unable to keep their jobs or research grants. Gofman has become the leader in the movement to protect the public against radiation, especially, since 1971, through the Committee for Nuclear Responsibility.
Gofman has said: “I was stupid in those days. In 1955, '56, people like Linus Pauling were saying that the bomb fallout would cause all this trouble. I thought, We're not sure. If you're not sure, don't stand in the way of progress. I could not have thought anything more stupid in my life.”
“The big moment in my life happened while I was giving a health lecture to nuclear engineers. In the middle of my talk it hit me! What the hell am I saying? If you don't know whether low doses are safe or not, going ahead is exactly wrong. At that moment, I changed my position entirely.”[17]
In 1979, Gofman said: “There is no way I can justify my failure to help sound an alarm over these activities many years sooner than I did. I feel that at least several hundred scientists trained in the biomedical aspect of atomic energy—myself definitely included—are candidates for Nuremberg-type trials for crimes against humanity for our gross negligence and irresponsibility. Now that we know the hazard of low-dose radiation, the crime is not experimentation—it's murder.” [18]
Many ordinary people were making exactly that argument in the 1950s, but government censorship kept the most incriminating evidence from the public. The climate of intimidation spread throughout the culture, so that teachers who spoke about the dangers of radiation were called disloyal, and were fired. Now, people who don't want x-rays are treated as crackpots. Probably because of this cultural situation, Gofman's recommendations are very mild—simply for doctors to use good technology and to know what they are doing, which could lead to ten-fold or even hundred-fold dose reduction. Even with such mild restraint in the use of diagnostic x-rays, Gofman's well founded estimate is that 250,000 deaths caused by radiation could be prevented annually. I believe many more deaths would be prevented if ultrasound and MRI were used consistently instead of x-rays. Using Gofman's estimate, I think we can blame at least ten million deaths on just the medical x-rays that have been used inappropriately because of the policies of the U.S. government in the last half century. That wouldn't include the deaths caused by radioactive fallout from bomb tests and leaks from nuclear power plants, or the vast numbers of people mentally impaired by all sorts of toxic radiation.
Although nearly all the people who committed the radiation crimes of the 1950s and 1960s have died or retired, the culture they created remains in the mass media and scientific journals, and in the medical and academic professions.
Medical journals describe ways to minimize diagnostic x-ray exposure, and they advocate many seemingly effective treatments for osteoporosis, giving an impression that progress is being made in “managing” osteoporosis, but the real situation is very different. Fractures resulting from osteoporosis are increasing, and osteoporosis is affecting younger and younger people. I think it would be reasonable to say that a woman with osteoporosis is usually better off when it's not diagnosed, because of the dangerous things prescribed for it. Estrogen has become the main “treatment” for osteoporosis, but many of the other ways of “managing” osteoporosis are both ineffective and unsafe.
Many women are told to stop taking a thyroid supplement when osteoporosis is diagnosed, but hypothyroidism often leads to hyperprolactinema and hypercortisolemia, which are two of the most clearly established causes of osteoporosis. Calcitonin, vitamin D-active metabolite, and estrogen-“HRT” treatments can cause respiratory alkalosis (relative hyperventilation),[19][20][21][22][23][24] and hypothyroidism produces a predisposition to hyperventilation.[25] Hyperventilation tends to cause calcium loss. In respiratory alkalosis, CO2 (and sometimes bicarbonate) are decreased, impairing calcium retention, and in “metabolic alkalosis,” with increased bicarbonate, calcium is retained more efficiently and bone formation is stimulated, and its dissolution is suppressed.
Other women are told to reduce their protein consumption, or to take fluoride or whatever drug has been most recently promoted. A protein deficiency is a clear cause of osteoporosis, and bone density corresponds to the amount of protein consumed. Milk protein, especially, protects against osteoporosis, independently of milk's other important nutrients. Too much fluoride clearly increases the risk of bone fractures,[26] and the side effects of other drugs haven't been properly studied in humans, while they often have dangerous effects in animals.
Calcium, magnesium, vitamin A, vitamin B6, vitamin K, and vitamin D are important for the development and maintenance of bones. For example, a vitamin A deficiency limits the synthesis of progesterone and proteins. In calcium deficiency, parathyroid hormone is increased, and tends to cause the typical changes of aging, shifting calcium from hard tissues to soft, and decreasing the ratio of extracellular to intracellular (excitatory) calcium.
Polyunsaturated fats are converted to prostaglandins (especially under the influence of estrogen), and several prostaglandins have toxic effects on bone. Those fats also suppress the formation of thyroid hormone and progesterone. The increased use of the unsaturated oils has coincided with the increase of osteoporosis.
The oxidation of proteins caused by free radicals is increased with aging and by the use of unsaturated fats, and it contributes to tissue atrophy, including the age-related shrinkage of the bones. In animal studies, “adequate” dietary protein, 13.8% of the diet (equivalent to about 80 g/text for a person) is associated with more oxidative damage to tissue proteins than the very high protein diets, 25.7% or 51.3%, that would be equivalent to about 150 or 300 g of protein daily for a person.[27] Yet, many physicians recommend a low protein diet to protect against osteoporosis.
Avoiding fluoridated water and the polyunsaturated oils, and drinking two quarts of milk daily (which will provide only 66 g of protein), and using some other nutrient-rich foods such as eggs and fruits, are probably the basic things to protect the bones. For vitamins, especially K, occasional liver can be helpful. Meats, fruits, leaves, and coffee are rich in magnesium.
Some people have argued that the acidity of urine produced by eating meat causes calcium loss. However, a high protein diet also improves the absorption of calcium by the intestine. Another overlooked function of dietary protein is that it stimulates insulin secretion, and insulin is anabolic for bone.[28]
The same diet that protects against osteoporosis, i.e., plenty of protein and calcium, etc., also protects against kidney stones and other abnormal calcifications.
References
[edit]- ↑ Kassem M.; Okazaki R.; León D. D.; Harris S. A.; Robinson J. A.; Spelsberg T. C.; Conover C. A.; Riggs B. L. Potential Mechanism of Estrogen-Mediated Decrease in Bone Formation: Estrogen Increases Production of Inhibitory Insulin-Like Growth Factor-Binding Protein-4. Proceedings of the Association of American Physicians 108(2), 155–64, 1996. https://pubmed.ncbi.nlm.nih.gov/8705735
- ↑ Galloway A.; Stini W. A.; Fox S. C.; Stein P. Stature Loss among an Older United States Population and Its Relation to Bone Mineral Status. American Journal of Physical Anthropology 83(4), 467–476, 1990. DOI: 10.1002/ajpa.1330830408
- ↑ Andresen R.; Radmer S.; Banzer D.; Felsenberg D.; Wolf K. Quantitative Knochenmineralgehaltsbestimmung (QCT)- Systemvergleich Baugleicher Computertomographen. RöFo- Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren 160(03), 260–265, 1994. DOI: 10.1055/s-2008-1032417
- ↑ Slosman D. O.; Rizzoli R.; Donath A.; Bonjour J. Vertebral Bone Mineral Density Measured Laterally by Dual-Energy X-Ray Absorptiometry. Osteoporosis International 1(1), 23–29, 1990. DOI: 10.1007/bf01880412
- ↑ Slosman D. O.; Rizzoli R.; Buchs B.; Piana F.; Donath A.; Bonjour J. Comparative Study of the Performances of X-Ray and Gadolinium 153 Bone Densitometers at the Level of the Spine, Femoral Neck and Femoral Shaft. European Journal of Nuclear Medicine 17(1-2), 3–9, 1990. DOI: 10.1007/bf00819396
- ↑ Henschel M. G.; Freyschmidt J.; Holland B. R. [Experimental Studies of the Visualization of the Vertebral Body Spongiosa by High-Resolution Computed Tomography]. Rofo: Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin 162(4), 269–73, 1995.
- ↑ Firooznia H.; Golimbu C.; Rafil M.; Schwartz M. S.; Alterman E. R. Quantitative Computed Tomography Assessment of Spinal Trabecular Bone. I. Age-Related Regression in Normal Men and Women. Journal of Computed Tomography 8(2), 91–97, 1984. DOI: 10.1016/0149-936x(84)90091-290091-2)
- ↑ Johnson J.; Dawson-Hughes B. Precision and Stability of Dual-Energy X-Ray Absorptiometry Measurements. Calcified Tissue International 49(3), 174–178, 1991. DOI: 10.1007/bf02556113
- ↑ Whitehouse R. W.; Economou G.; Adams J. E. Influence of Temperature on QCT. Journal of Computer Assisted Tomography 17(6), 945–951, 1993. DOI: 10.1097/00004728-199311000-00017
- ↑ Merritt R. B.; Chenery S. G. Quantitative CT Measurements: The Effect of Scatter Acceptance and Filter Characteristics on the EMI 7070. Physics in Medicine and Biology 31(1), 55–63. DOI: 10.1088/0031-9155/31/1/005
- ↑ Epstein D. M.; Dalinka M. K.; Kaplan F. S.; Aronchick J. M.; Marinelli D. L.; Kundel H. L. Observer Variation in the Detection of Osteopenia. Skel Radiology 15(5), 347–349, 1986. DOI: 10.1007/bf00348859
- ↑ Schneider P.; Reiners C. Changes in Bone Mineral Density in Male Athletes. JAMA 277(1), 23, 1997.
- ↑ Dawson-Hughes B.; Dallal G. E. Effect of Radiographic Abnormalities on Rate of Bone Loss from the Spine. Calcified Tissue International 46(4), 280–281, 1990. DOI: 10.1007/bf02555008
- ↑ Jaworski M.; Lorenc R. S. [Progress in Measurement of the Calcaneus Using Ultrasonic Methods in Children and Adolescents]. Przeglad Lekarski 57(2), 93–9, 2000.
- ↑ He Y. Q.; Fan B.; Hans D.; Li J.; Wu C. Y.; Njeh C. F.; Zhao S.; Lu Y.; Tsuda-Futami E.; Fuerst T.; Genant H. K. Assessment of a New Quantitative Ultrasound Calcaneus Measurement: Precision and Discrimination of Hip Fractures in Elderly Women Compared with Dual X-Ray Absorptiometry. Osteoporosis International 11(4), 354–360. DOI: 10.1007/s001980070125
- ↑ Michalská D.; Zikán V.; Štěpán J.; Weichetová M.; Kubová V.; Krenková J.; Masatová A. [X-Ray Densitometry and Ultrasonography of the Heel Bone–Sensitivity and Comparison with Densitometry of the Axial Skeleton]. Casopis Lekaru Ceskych 139(8), 231–6, 2000. https://pubmed.ncbi.nlm.nih.gov/10916211
- ↑ Terkel S. Gofman, John W. Coming of Age: The Story of Our Century by Those Who've Lived It 401–412, 1995.
- ↑ Gofman J. W. Irrevy: An Irreverent, Illustrated View of Nuclear Power: A Collection of Talks, from Blunderland to Seabrook IV. Committee for Nuclear Responsibility, 1979.
- ↑ Krapf R.; Jaeger P.; Hulter H. N.; Fehlman C.; Takkinen R. Chronic Respiratory Alkalosis Induces Renal PTH-Resistance, Hyperphosphatemia and Hypocalcemia in Humans. Kidney International 42(3), 727–734, 1992. DOI: 10.1038/ki.1992.340
- ↑ Orr-Walker B. J. Hormone Replacement Therapy Causes a Respiratory Alkalosis in Normal Postmenopausal Women. Journal of Clinical Endocrinology Metabolism 84(6), 1997–2001. DOI: 10.1210/jc.84.6.1997
- ↑ Schabel F. M.; Zieglauer H. [Investigations on the Pathogenesis of Distal Renal Tubular Acidosis]. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) 91(9), 304–7, 1979. http://www.hebrewbooks.org/36716
- ↑ Locatto M. E.; Fernandez M. C.; Caferra D. A.; Gimenez M. C.; Vidal M. C.; Puche R. C. Respiratory Alkalosis and Reduced Plasmatic Concentration of Ionized Calcium in Rats Treated with 1,25 Dihydroxycholecalciferol. Calcified Tissue International 36(1), 604–607, 1984. DOI: 10.1007/bf02405374
- ↑ Bushinsky D. A. Metabolic Alkalosis Decreases Bone Calcium Efflux by Suppressing Osteoclasts and Stimulating Osteoblasts. American Journal of Physiology-Renal Physiology 271(1), F216-F222. DOI: 10.1152/ajprenal.1996.271.1.f216
- ↑ Unwin R.; Stidwell R.; Taylor S.; Capasso G. The Effects of Respiratory Alkalosis and Acidosis on Net Bicarbonate Flux along the Rat Loop of Henle in Vivo. American Journal of Physiology-Renal Physiology 273(5), F698-F705. DOI: 10.1152/ajprenal.1997.273.5.f698
- ↑ Lee H. T.; Levine M. Acute Respiratory Alkalosis Associated with Low Minute Ventilation in a Patient with Severe Hypothyroidism. Canadian Journal of Anesthesia/Journal canadien d'anesthésie 46(2), 185–189, 1999. DOI: 10.1007/bf03012556
- ↑ Sowers M. R.; Clerk K. M.; Jannausch M. L.; Wallace R. B. A Prospective Study of Bone Mineral Content and Fracture in Communities with Differential Fluoride Exposure. American Journal of Epidemiology 133(7), 649–660. DOI: 10.1093/oxfordjournals.aje.a115940
- ↑ Petzke K. J.; Elsner A.; Proll J.; Thielecke F.; Metges C. C. Long-Term High Protein Intake Does not Increase Oxidative Stress in Rats. The Journal of Nutrition 130(12), 2889–2896, 2000. DOI: 10.1093/jn/130.12.2889
- ↑ McCarty M. Anabolic Effects of Insulin on Bone Suggest a Role for Chromium Picolinate in Preservation of Bone Density. Medical Hypotheses 45(3), 241–246, 1995. DOI: 10.1016/0306-9877(95)90112-490112-4)