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Hossam Zero Holes (HZH) Unravel Osteoporosis Roots and the coincidental Soft Tissue Calcification in the Elderly: Granted US Patent Review

Published in Frontiers (Volume 1, Issue 4)
Received: 10 December 2021    Accepted: 21 December 2021    Published: 29 December 2021
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Abstract

The mineralization of the bone is the most important step in its strengthening & preventing its fracture. Calcium is by far the most important and most predominant mineral inside the bone. There is a wrong concept that blood calcium always has access to the bone. This is the basis of calcium supplementation in the elderly or patients with low bone mineral density (BMD). There is an increasing evidence that low BMD is almost always associated with soft tissue calcification. This is why the precipitating factors predisposing to low BMD may have a role in soft tissue calcification. For the calcium to be fixed in the bone, it needs collaboration from all its components namely, the functional collagen, the apatite chips, and the bone cells. The most fundamental point is the zero holes and the zero channels of the collagen bundles. Other factors that could modulate bone mineralization are outside the bone. These extra-osseous parameters act as adjuvants or co-factors that can modify the process of bone mineralization. By the same token, these co-factors may lead to soft tissue calcification. These adjuvant co-factors include hormonal status, visceral fat, hyperinsulinemia, and some minerals in the serum other than calcium itself. If these co-factors are not in an optimal condition for the bone, they would induce low BMD. Therefore, calcium supplementation is not always the right choice in cases of low BMD. This is because it may exaggerate the consequential soft tissue calcification. The US patent (US9801905) suggests that calcium can be supplemented in low BMD only if the bone is prepared to accept the calcium. The molecular mechanics of the zero holes and the orientation of the apatite chips help in the better understanding of the mechanism of bone mineralization & the associated soft tissue calcification

Published in Frontiers (Volume 1, Issue 4)
DOI 10.11648/j.frontiers.20210104.18
Page(s) 112-120
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Zero Holes, Virtual Gate, DEXA, BMD, Zero Channels, Apatite Chips

References
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[2] Kun Zhu. 2012. Calcium and Bone. Clinic Biochem. 45 (12): 936-42.
[3] Rinaldo Florencio-Silva. 2015. Biology of Bone Tissue: Structure, Function, and Factors That Influence Bone Cells. Biomedical research international. 421746.
[4] Andrew J. Spiro. 2019. ARTIFACTS AFFECTING DUAL-ENERGY X-RAY ABSORPTIOMETRY MEASUREMENTS. AACE clinical case Reports. 5 (4): e263–e266.
[5] FriedaFeldman. 1986. Soft tissue mineralization: Roentgen analysis. Current problems in diagnostic radiology. Volume 15, Issue 3. Pages 166-240.
[6] Dimitrios J Hadjidakis, 2006. Bone Remodeling. Women's Health and Disease: Gynecologic, Endocrine, and Reproductive. Volume 1092, Issue 1. Pages 385-396.
[7] Stuart H Ralston. 2015. Diagnosis and Management of osteoporosis. Practitioner. 259 (1788): 15-9, 2.
[8] E. Legrand. 1999. Bone Mineral Density and Vertebral Fractures in Men. Osteoporosis International. 10, pages 265–270.
[9] Hossam Mohamed. 2017. Use of organic sulphur, antioxidants, and amino acids in conjunction with exercise and electromagnetic stimulation to treat osteoporosis. US patent. US9801905. https://patents.google.com/patent/US9801905B2/en.
[10] Hossam Mohamed. 2021. Hossam Osteonic Circulation (HOC) Deciphers the Root Causes of osteoporosis & Reveals the Hidden Secrets of the Physiological Lines of Its Treatment: US Patent Review. Frontiers. Volume 1, Issue 4, December 2021, Pages: 89-99.
[11] R G Paul. 1996. Glycation of collagen: the basis of its central role in the late complications of ageing and diabetes. The International Journal of Biochemistry & Cell Biology. Volume 28, Issue 12, Pages 1297-1310.
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[17] Daniel D. Bikle. 2012. Vitamin D and Bone. Current Osteoporosis Reports volume 10, pages 151–159.
[18] Chen-Yuan Hsiao, 2020. Calcitonin Induces Bone Formation by Increasing Expression of Wnt10b in Osteoclasts in Ovariectomy-Induced Osteoporotic Rats. Frontiers Endocrinology. Volume 11. Article 613.
[19] G Lombardi. 2011. The roles of parathyroid hormone in bone remodeling: prospects for novel therapeutics. J Endocrinol Invest vol 34 (7 Suppl): 18-22.
[20] Yahtyng Sheu. 2014. The Role of Bone Marrow and Visceral Fat on Bone Metabolism. Curr Osteoporos Rep. 9 (2): 67–75.
[21] Kaisa K Ivaska. 2015. The effects of acute hyperinsulinemia on bone metabolism. Endocrinal Connections. Vol 4 (3): 155–162.
[22] Sara Castiglioni. 2013. Magnesium and Osteoporosis: Current State of Knowledge and Future Research Directions. Nutrients. 5 (8): 3022–3033.
[23] J. Patrick O’Connor. 2020. Zinc as a Therapeutic Agent in Bone Regeneration. Materials (Basel). vol. 13 (10): 2211.
[24] Xinhua Qu. 2018. Serum copper levels are associated with bone mineral density and total fracture. J Orthopedic Translation. 14: 34–44.
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[27] Hossam Mohamed, 2017. Use of organic sulphur, antioxidants, and amino acids in conjunction with exercise and electromagnetic stimulation to treat osteoporosis. https://pubchem.ncbi.nlm.nih.gov/patent/US9801905.
Cite This Article
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    Hossam Mohamed, Houda Almansour, Dalal Alsaadoun, Mariam Almansour, Sulaiman Alnassera. (2021). Hossam Zero Holes (HZH) Unravel Osteoporosis Roots and the coincidental Soft Tissue Calcification in the Elderly: Granted US Patent Review. Frontiers, 1(4), 112-120. https://doi.org/10.11648/j.frontiers.20210104.18

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    ACS Style

    Hossam Mohamed; Houda Almansour; Dalal Alsaadoun; Mariam Almansour; Sulaiman Alnassera. Hossam Zero Holes (HZH) Unravel Osteoporosis Roots and the coincidental Soft Tissue Calcification in the Elderly: Granted US Patent Review. Frontiers. 2021, 1(4), 112-120. doi: 10.11648/j.frontiers.20210104.18

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    AMA Style

    Hossam Mohamed, Houda Almansour, Dalal Alsaadoun, Mariam Almansour, Sulaiman Alnassera. Hossam Zero Holes (HZH) Unravel Osteoporosis Roots and the coincidental Soft Tissue Calcification in the Elderly: Granted US Patent Review. Frontiers. 2021;1(4):112-120. doi: 10.11648/j.frontiers.20210104.18

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  • @article{10.11648/j.frontiers.20210104.18,
      author = {Hossam Mohamed and Houda Almansour and Dalal Alsaadoun and Mariam Almansour and Sulaiman Alnassera},
      title = {Hossam Zero Holes (HZH) Unravel Osteoporosis Roots and the coincidental Soft Tissue Calcification in the Elderly: Granted US Patent Review},
      journal = {Frontiers},
      volume = {1},
      number = {4},
      pages = {112-120},
      doi = {10.11648/j.frontiers.20210104.18},
      url = {https://doi.org/10.11648/j.frontiers.20210104.18},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.frontiers.20210104.18},
      abstract = {The mineralization of the bone is the most important step in its strengthening & preventing its fracture. Calcium is by far the most important and most predominant mineral inside the bone. There is a wrong concept that blood calcium always has access to the bone. This is the basis of calcium supplementation in the elderly or patients with low bone mineral density (BMD). There is an increasing evidence that low BMD is almost always associated with soft tissue calcification. This is why the precipitating factors predisposing to low BMD may have a role in soft tissue calcification. For the calcium to be fixed in the bone, it needs collaboration from all its components namely, the functional collagen, the apatite chips, and the bone cells. The most fundamental point is the zero holes and the zero channels of the collagen bundles. Other factors that could modulate bone mineralization are outside the bone. These extra-osseous parameters act as adjuvants or co-factors that can modify the process of bone mineralization. By the same token, these co-factors may lead to soft tissue calcification. These adjuvant co-factors include hormonal status, visceral fat, hyperinsulinemia, and some minerals in the serum other than calcium itself. If these co-factors are not in an optimal condition for the bone, they would induce low BMD. Therefore, calcium supplementation is not always the right choice in cases of low BMD. This is because it may exaggerate the consequential soft tissue calcification. The US patent (US9801905) suggests that calcium can be supplemented in low BMD only if the bone is prepared to accept the calcium. The molecular mechanics of the zero holes and the orientation of the apatite chips help in the better understanding of the mechanism of bone mineralization & the associated soft tissue calcification},
     year = {2021}
    }
    

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    AB  - The mineralization of the bone is the most important step in its strengthening & preventing its fracture. Calcium is by far the most important and most predominant mineral inside the bone. There is a wrong concept that blood calcium always has access to the bone. This is the basis of calcium supplementation in the elderly or patients with low bone mineral density (BMD). There is an increasing evidence that low BMD is almost always associated with soft tissue calcification. This is why the precipitating factors predisposing to low BMD may have a role in soft tissue calcification. For the calcium to be fixed in the bone, it needs collaboration from all its components namely, the functional collagen, the apatite chips, and the bone cells. The most fundamental point is the zero holes and the zero channels of the collagen bundles. Other factors that could modulate bone mineralization are outside the bone. These extra-osseous parameters act as adjuvants or co-factors that can modify the process of bone mineralization. By the same token, these co-factors may lead to soft tissue calcification. These adjuvant co-factors include hormonal status, visceral fat, hyperinsulinemia, and some minerals in the serum other than calcium itself. If these co-factors are not in an optimal condition for the bone, they would induce low BMD. Therefore, calcium supplementation is not always the right choice in cases of low BMD. This is because it may exaggerate the consequential soft tissue calcification. The US patent (US9801905) suggests that calcium can be supplemented in low BMD only if the bone is prepared to accept the calcium. The molecular mechanics of the zero holes and the orientation of the apatite chips help in the better understanding of the mechanism of bone mineralization & the associated soft tissue calcification
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Author Information
  • Medical & Research Department, Huda Health INC, Ottawa, Canada

  • Medical & Research Department, Huda Health INC, Ottawa, Canada

  • Internal Medicine Department, College of Medicine, King Faisal University, Alahsa, Saudi Arabia

  • Department of Endocrinology, AlFaisalia Hospital, Alhafouf City, Saudi Arabia

  • Department of Pharmacology and Toxicology, Unaizah College of Pharmacy, Qassim University, Buraydah, Saudi Arabia

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