Senile Osteoporosis: the Involvement of Differentiation and Senescence of Bone Marrow Stromal Cells

Total Page:16

File Type:pdf, Size:1020Kb

Senile Osteoporosis: the Involvement of Differentiation and Senescence of Bone Marrow Stromal Cells International Journal of Molecular Sciences Review Senile Osteoporosis: The Involvement of Differentiation and Senescence of Bone Marrow Stromal Cells Abdul Qadir 1,2,3, Shujing Liang 1,2,3, Zixiang Wu 1,2,3, Zhihao Chen 1,2,3, Lifang Hu 1,2,3,* and Airong Qian 1,2,3,* 1 Laboratory for Bone Metabolism, Key Laboratory for Space Biosciences and Biotechnology, School of Life Sciences, Northwestern Polytechnical University, Xi’an 710072, China; [email protected] (A.Q.); [email protected] (S.L.); [email protected] (Z.W.); [email protected] (Z.C.) 2 Research Center for Special Medicine and Health Systems Engineering, School of Life Sciences, Northwestern Polytechnical University, Xi’an 710072, China 3 NPU-UAB Joint Laboratory for Bone Metabolism, School of Life Sciences, Northwestern Polytechnical University, Xi’an 710072, China * Correspondence: [email protected] (L.H.); [email protected] (A.Q.); Tel.: +86-29-88491840 (A.Q.) Received: 13 December 2019; Accepted: 31 December 2019; Published: 5 January 2020 Abstract: Senile osteoporosis has become a worldwide bone disease with the aging of the world population. It increases the risk of bone fracture and seriously affects human health. Unlike postmenopausal osteoporosis which is linked to menopause in women, senile osteoporosis is due to aging, hence, affecting both men and women. It is commonly found in people with more than their 70s. Evidence has shown that with age increase, bone marrow stromal cells (BMSCs) differentiate into more adipocytes rather than osteoblasts and undergo senescence, which leads to decreased bone formation and contributes to senile osteoporosis. Therefore, it is necessary to uncover the molecular mechanisms underlying the functional changes of BMSCs. It will benefit not only for understanding the senile osteoporosis development, but also for finding new therapies to treat senile osteoporosis. Here, we review the recent advances of the functional alterations of BMSCs and the related mechanisms during senile osteoporosis development. Moreover, the treatment of senile osteoporosis by aiming at BMSCs is introduced. Keywords: senile osteoporosis; bone marrow stromal cells; differentiation; senescence; treatment 1. Introduction The word “osteoporosis” means “porous bone”, which is actually a worldwide metabolic bone disorder with high incidence. It is characterized by decreased bone mass, increased bone fragility and deteriorated microstructural bone tissues [1]. It occurs due to the imbalance between bone formation and bone resorption [2]. Although it has been observed in all races, gender and age groups, but more commonly found in women and older people [3]. It remains hidden until being revealed as a disorder through bone fractures, due to minor strokes [4]. It is considered amongst the most common human diseases associated with bone fractures and other severe secondary major health problems. According to the recent report of National Osteoporosis Foundation (NOF), every second woman and fourth man worldwide over the age of 50 years will encounter bone fracture, due to osteoporosis in their remaining lives. Osteoporosis is generally divided into two forms, primary osteoporosis and secondary osteoporosis. The primary osteoporosis mainly contains three categories, juvenile, postmenopausal, and senile Int. J. Mol. Sci. 2020, 21, 349; doi:10.3390/ijms21010349 www.mdpi.com/journal/ijms Int. J. Mol. Sci. 2020, 21, 349 2 of 23 osteoporosis, while the secondary osteoporosis is mainly caused by a large number of diseases and medications [5]. The primary osteoporosis is more common than the second one, and the senile osteoporosis has become one significant health concern of the world as it is an age-related disorder that occursInt. J. Mol. in Sci. people’s 2019, 20, x 70s,FOR PEER leading REVIEW to the attenuation of both the cortical and trabecular bones2 of 22 [6 ]. Besidesthe senile the osteoporosis imbalance has between become boneone significant formation health conducted concern of by the osteoblasts world as it and is an bone age-related resorption conducteddisorder by that osteoclasts, occurs in evidence people’s demonstrates70s, leading to thatthe changesattenuation in numberof both the and cortical function and of trabecular bone marrow stromalbones cells [6]. (BMSCs) are also one key cause for senile osteoporosis [7]. Study shows that BMSCs normallyBesides differentiate the imbalance in a proper between manner bone into formation osteoblast, conducted chondrocytes by osteoblasts and and adipocytes, bone resorption but during old ages,conducted there isby comparatively osteoclasts, evidence less di ffdemonstrateserentiation ofthat BMSCs changes into in osteoblast number and than function adipocytes. of bone Such a shift inmarrow cell di stromalfferentiation cells (BMSCs) of BMSCs are also results one inkey reduced cause for bone senile formation, osteoporosis which [7]. Study contributes shows that to senile osteoporosisBMSCs normally (Figure 1differentiate)[ 8]. The underlyingin a proper manner mechanism into osteoblast, behind this chondrocytes abnormal and decision adipocytes, in old but ages is during old ages, there is comparatively less differentiation of BMSCs into osteoblast than adipocytes. still under investigation. However, some achievements have been made in the form of identification Such a shift in cell differentiation of BMSCs results in reduced bone formation, which contributes to of peroxisome proliferator-activated receptor γ (PPARγ) and core binding factor α1 (CEBPα/β/δ) as senile osteoporosis (Figure 1) [8]. The underlying mechanism behind this abnormal decision in old masterages regulators is still under of di ffinvestigation.erentiation toward However, adipogenesis, some achievements while Osterix have been and runt-relatedmade in the transcriptionform of factoridentification 2 (Runx2) toward of peroxisome osteogenesis proliferator-activated [9]. In addition, receptor recent evidence γ (PPARγ demonstrates) and core binding that the factor senescence α1 of BMSCs(CEBP isα/ alsoβ/δ) oneas master important regulators cause of of differentiation senile osteoporosis toward adipogenesis, (Figure1). Cellular while Osterix senescence and runt- was first discoveredrelated bytranscription Hayflick in factor the 1960s, 2 (Runx2) which istoward a phenomenon osteogenesis where [9]. theIn cellsaddition, halt torecent divide evidence in response to variousdemonstrates stresses that causing the senescence DNA damage, of BMSCs and is begin also one to secreteimportant chemokines, cause of senile cytokines, osteoporosis and extracellular (Figure matrix1). proteins,Cellular senescence creating a was toxic first microenvironment discovered by Hayflick called in senescence-associatedthe 1960s, which is a phenomenon secretory phenotypewhere (SASP)the [ 10cells]. Suchhalt to toxicity divide ofin SASPresponse affects to various neighboring stresses normal causing cells, DNA resulting damage, inand further begin senescentto secrete cells chemokines, cytokines, and extracellular matrix proteins, creating a toxic microenvironment called accumulation, and thus, damage the residing tissue [11]. The expression of senescence biomarker senescence-associated secretory phenotype (SASP) [10]. Such toxicity of SASP affects neighboring p16Ink4anormal is cells, also resulting enhanced in [further12]. Cellular senescent senescence cells accumulation, has been and demonstrated thus, damage the to playresiding a crucial tissue role in age-related[11]. The expression pathologies, of senescence such as biomarker atherosclerosis, p16Ink4a type is also II diabetes,enhanced Alzheimer’s,[12]. Cellular senescence and Parkinson’s has diseasesbeen [ 13demonstrated]. Like the to senescence play a crucial of otherrole in cells age-related associated pathologies, with age-related such as atherosclerosis, pathologies, type the II exact mechanismdiabetes, behind Alzheimer’s, BMSCs and senescence Parkinson’s during diseases senile [13]. osteoporosis Like the senescence is still unclear.of other However,cells associated telomere shortening,with age-related oxidative stresspathologies, and some the geneticexact mechan and epigeneticism behind regulations BMSCs havesenescence been foundduring to senile contribute to BMSCsosteoporosis senescence is still during unclear. senile However, osteoporosis telomere shortening, [14]. Therefore, oxidative both stress abnormal and some diff erentiationgenetic and and senescenceepigenetic of BMSCs regulations lead have to the been reduced found to number contribute of osteoblaststo BMSCs senescence in old ages, during which senile result osteoporosis in decreased bone[14]. formation, Therefore, thus, both cause abnormal senile differentiation osteoporosis. and senescence of BMSCs lead to the reduced number of osteoblasts in old ages, which result in decreased bone formation, thus, cause senile osteoporosis. Figure 1. Schematic diagram of differentiation and senescence of bone marrow stromal cells (BMSCs) Figure 1. Schematic diagram of differentiation and senescence of bone marrow stromal cells (BMSCs) during senile osteoporosis. during senile osteoporosis. Int. J. Mol. Sci. 2020, 21, 349 3 of 23 To date, numerous medicines have been used to treat senile osteoporosis, but there are still some limitations, due to their side effects [15–19]. Therefore, in order to find out proper treatments, it is the focus of new era cell-based therapy research to uncover the molecular mechanisms behind the differentiation and senescence of BMSCs. Here, we
Recommended publications
  • Clinico-Biochemical Study on Senile Osteoporosis
    Nagoya ]. med. Sci. 28: 110-125, 1965 CLINICO-BIOCHEMICAL STUDY ON SENILE OSTEOPOROSIS MAsAsHr NAKAGAWA, RErsuKE NATSUME, ToHRU YosHIDA, MrTsUNOBU SaroNO, OsAMU KmA, HrsASHI IwATA, AND HrsASHI HrRAKOH Department of Orthopedic Surgery, Nagoya University School of Medicine (Director: Prof. Masashi Nakagawa) KEIICHI KASAHARA Department of Orthopedic Surgery, Wakayama Medical College Osteoporosis, except that occurring secondarily to known pathogenesis, is termed senile or postmenopausal osteoporosis and arises from a still unknown cause. Primary osteoporosis may occur as a result of adrenal-gonadal imbalance or of calcium deficiency. However since these pathogenetical views are· disagreed with by many other investigators, the cause remains unproven and this clinical diagnosis lacks objective basis. At this stage, determination as to whether senile osteoporosis represents only one aspect of the physiological aging process or is independent pathological entity seems to be of definite clinical interest. In this study total serum hexosamine content in normal subjects was found to increase with advancing age. Especially, the ratio by weight of glucosamine to galactosamine in the sera decreases with increasing age until fourty-nine years of age, but beyond this age limit the ratio significantly increased. On the other hand the ratio of the serum glucosamine to galactosamine was shown to be significantly low in patients with senile osteoporosis as compared with the ratio in normal group of identical age. Also, increased urinary hydroxyproline excretion in senile osteo­ porosis as evidenced in this study appeared to suggest collagen degradation. The present study has found evidences of abnormal mucopolysaccharide metabolism and collagen degradation in osteoporotic patients. These observations suggest that senile osteoporosis, whatever the true cause may be, is an independent pathological entity rather than a simple result of senile metabolic decay.
    [Show full text]
  • Family Practice Grand Rounds Postmenopausal
    Family Practice Grand Rounds Postmenopausal Osteoporosis and Estrogen Therapy: Who Should Be Treated? Lombardo F. Palma, MD Salt Lake City, Utah DR. LOMBARDO F. PALMA (Robert Wood It is estimated that 25 percent of white women Johnson Foundation Fellow, Department of Fam­ by the age of 65 years and 50 percent by the age of ily and Community Medicine): The objective of 75 years will have vertebral fractures, by far the Grand Rounds today is to discuss the cognitive most common complication in osteoporotic post­ process by which the family physician can make a menopausal women. Hip fractures have also been rational decision about estrogen therapy in post­ related to osteoporosis, and they are at least two menopausal women. I will briefly present some times more frequent in women than in men, de­ facts about osteoporosis, the physiology of meno­ pending on the age group.1 In the United States pause and subsequent bone demineralization, the there are about 200,000 hip fractures a year at an characteristics of women at risk of developing estimated cost of over one billion dollars, and 75 osteoporosis, and the therapeutic alternatives, as percent of those are probably due to osteoporosis. well as their risks and benefits. Then we will open Hip fractures are related to a high death rate in the the discussion. elderly (16 percent die within six months).1 This is a public health issue, as there are about four mil­ lion women in the United States who are sympto­ matic from osteoporotic fractures. From the Department of Family and Community Medicine, Menopause is the result of a sharp decline in the University of Utah Medical Center, Salt Lake City, Utah.
    [Show full text]
  • Current and Potential Future Drug Treatments for Osteoporosis
    700 Annals ofthe Rheumatic Diseases 1996;55:700-714 REVIEW Ann Rheum Dis: first published as 10.1136/ard.55.10.700 on 1 October 1996. Downloaded from Current and potential future drug treatments for osteoporosis Sanjeev Patel Osteoporosis is the most common metabolic ture risk increases by a factor of 1.5 to 3.0.6 bone disease in the developed world and is Other determinants of osteoporotic fracture increasingly recognised as an important public are shown in table 1. health problem.' There is marked worldwide Drugs active on bone can be simplistically variation in its incidence. It is predicted that classified as those that inhibit bone resorption the incidence of hip fractures caused by or those that stimulate bone formation (table osteoporosis will increase, particularly in 2). The effects of these drugs on bone mineral developing countries.2 The human burden of density are summarised in fig 1. Drugs that osteoporosis is considerable, with increased stimulate bone formation lead to a direct morbidity and mortality, especially following increase in bone mineral density, whereas those osteoporotic hip fractures.' The current finan- that inhibit bone resorption result in limited cial burden is substantial, with estimated yearly increases in bone mineral density by costs of £750 million in the UK,' $10 billion in uncoupling bone turnover and allowing forma- the USA, and FF3.7 billion in France.3 The tion to continue in excess of resorption. This ability to measure bone mineral density and leads to an increase in bone mineral density thereby monitor response to intervention has due to filling in of the remodelling space (the been vital in the development ofpharmacologi- remodelling transient).7 It has been suggested cal treatments.
    [Show full text]
  • Bone Health in Estrogen-Free Contraception
    Osteoporosis International (2019) 30:2391–2400 https://doi.org/10.1007/s00198-019-05103-6 REVIEW Bone health in estrogen-free contraception P. Hadji1,2 & E. Colli3 & P.-A. Regidor 4 Received: 11 May 2019 /Accepted: 18 July 2019 /Published online: 24 August 2019 # International Osteoporosis Foundation and National Osteoporosis Foundation 2019 Abstract Estrogens and progestogens influence the bone. The major physiological effect of estrogen is the inhibition of bone resorption whereas progestogens exert activity through binding to specific progesterone receptors. New estrogen-free contraceptive and its possible implication on bone turnover are discussed in this review. Insufficient bone acquisition during development and/or accelerated bone loss after attainment of peak bone mass (PBM) are 2 processes that may predispose to fragility fractures in later life. The relative importance of bone acquisition during growth versus bone loss during adulthood for fracture risk has been explored by examining the variability of areal bone mineral density (BMD) (aBMD) values in relation to age. Bone mass acquired at the end of the growth period appears to be more important than bone loss occurring during adult life. The major physiological effect of estrogen is the inhibition of bone resorption. When estrogen transcription possesses binds to the receptors, various genes are activated, and a variety modified. Interleukin 6 (IL-6) stimulates bone resorption, and estrogen blocks osteoblast synthesis of IL- 6. Estrogen may also antagonize the IL-6 receptors. Additionally, estrogen inhibits bone resorption by inducing small but cumu- lative changes in multiple estrogen-dependent regulatory factors including TNF-α and the OPG/RANKL/RANK system.
    [Show full text]
  • Management of Chronic Pain in Osteoporosis: Challenges and Solutions
    Journal of Pain Research Dovepress open access to scientific and medical research Open Access Full Text Article REVIEW Management of chronic pain in osteoporosis: challenges and solutions Teresa Paolucci* Abstract: Osteoporosis (OP) is a pathological condition that manifests clinically as pain, Vincenzo Maria Saraceni fractures, and physical disability, resulting in the loss of independence and the need for long- Giulia Piccinini* term care. Chronic pain is a multidimensional experience with sensory, affective, and cognitive aspects. Age can affect each of these dimensions and the pain that is experienced. In OP, chronic Physical Medicine and Rehabilitation Unit, Azienda Policlinico Umberto I, pain appears to have sensory characteristics and properties of nociceptive and neuropathic pain. Rome, Italy Its evaluation and treatment thus require a holistic approach that focuses on the specific character- *These authors contributed equally to istics of this population. Pain management must therefore include pharmacological approaches, this work physiotherapy interventions, educational measures, and, in rare cases, surgical treatment. Most rehabilitative treatments in the management of patients with OP do not evaluate pain or physi- For personal use only. cal function, and there is no consensus on the effects of rehabilitation therapy on back pain or quality of life in women with OP. Pharmacological treatment of pain in patients with OP is usually insufficient. The management of chronic pain in patients with OP is complicated with regard to its diagnosis, the search for reversible secondary causes, the efficacy and duration of oral bisphosphonates, and the function of calcium and vitamin D. The aim of this review is to discuss the most appropriate solutions in the management of chronic pain in OP.
    [Show full text]
  • Changes of the Quality-Of-Life Under the Treatment of Severe Senile Osteoporosis with Teriparatide
    Archives of Gerontology and Geriatrics 49 (2009) 35–38 Contents lists available at ScienceDirect Archives of Gerontology and Geriatrics journal homepage: www.elsevier.com/locate/archger Changes of the quality-of-life under the treatment of severe senile osteoporosis with teriparatide Domenico Maugeri a,*, Enzo Russo b, Salvatore Luca a, Carmelo Leotta a, Grazia Mamazza a, Rosaria Sorace a, Maurizio Rizzotto a, Sara Manuele a, Valentina Fiore a, Giuseppe Taverna a, Biagio Castiglia a, Michele Calitro c a Department of Aging, Urological and Neurological Sciences, University of Catania, Cannizzaro Hospital, Via Messina 829, I-95126 Catania, Italy b Unita` Operativa Complessa di Geriatria e Lungodegenza di Patti, Via Mazzini, I-98066 Patti (Messina), Italy c Unita` Operativa Complessa di Geriatria, Ospedale Civile Caduti il Guerra Via Bovio, I-70053 Canosa di Puglia (Bari), Italy ARTICLE INFO ABSTRACT Article history: Despite being treated with antiresorptive drugs, the severe osteoporosis (SO) is being considered as a Received 12 December 2007 condition in which patients are still subject to one or more vertebral or femoral fractures, or non- Received in revised form 18 April 2008 vertebral or non-femoral fractures, i.e., of other parts of the body such as the wrist, shoulder, tibia, ribs or Accepted 22 April 2008 hip. These patients are defined as non-responders (NRs) to the antiresorptive therapy, and recent Available online 13 June 2008 research has shown that they represent 10–25% of all SO patients. During the last almost 3 years a new drug has become available in Italy, called teriparatide (rh-PTH-1-34), produced in Escherichia coli using Keywords: the recombinant-DNA technique.
    [Show full text]
  • Osteoporosis: It’S More Than Calcium
    J. Freeman & L Turner / Californian Journal of Health Promotion 2004, Volume 2, Issue 3, 12-29 Osteoporosis: It’s More Than Calcium Jeanne Freeman1 and Lori Turner2 1California State University, Chico 2University of Arkansas Abstract Osteoporosis is a major public health concern with millions of Americans being affected. This painful and oftentimes crippling disease is multifactorial in nature. Therefore, the development of osteoporosis is related to more issues than a person’s intake of calcium. As a result, osteoporosis is not age or gender dependent. Risk factors for osteoporosis include proper nutrition including calcium intake, heredity, age, gender, physical inactivity, smoking, excessive alcohol use, and the use of several medications. With such a variety of risk factors, everyone should assume risk for disease development and thus take steps for the prevention of this bone fragility disease. © 2004 Californian Journal of Health Promotion. All rights reserved. Keywords: osteoporosis, women’s health, health education, calcium intake Osteoporosis is a major public health concern in loss of function (Lappe, 1994; Turner, Taylor, & the United States. An estimated 28 million Hunt, 1998; Ullom-Minnich, 1999). The Americans are already afflicted with this disease financial costs associated with osteoporotic and approximately 1.5 million new fractures fractures include direct medical charges, occur each year (Barefield, 1996; Boughton, rehabilitation, and extended treatment facilities. 1999; Krall & Dawson-Hughes, 1999; National Osteoporosis-related hip fractures alone result in Institutes of Health (NIH), 2000). In addition to estimated costs of $12.8 billion to $17.8 billion those already afflicted, another 18 million per year. Rehabilitation and institutionalization Americans have low bone density, placing them account for approximately 40% of these costs at risk for this disorder (NIH, 2000).
    [Show full text]
  • Low-Level Laser Irradiation on Senile Osteoporosis in Rats
    European Review for Medical and Pharmacological Sciences 2017; 21: 5230-5238 Beneficial effects of low-level laser irradiation on senile osteoporosis in rats C.-T. ZHU1, T. LI2, P. ZHANG3, M. ZOU4, Q. GUO2, X.-W. QU1 1Laser Medical Center, The First People’s Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, Kunming, China 2Faculty of Medcine, Kunming University of Science and Technology, Department of Gastroenterology, The First People’s Hospital of Yunnan Province, Kunming, China 3The First Department of General Surgery, The First People’s Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, Kunming, China 4Department of Urology, The First People’s Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, Kunming, China Chongtao Zhu and Ting Li contributed equally to this work Abstract. – OBJECTIVE: To investigate the ef- strength of the femur in the old group; the bio- fect of low-level laser irradiation (LLLI) on bone chemical analysis showed that LLLI could sig- mineral density (BMD), bone structures, bone nificantly reduce Ca and P losses and elevate biomechanical properties and bone metabolism the levels of serum BAP and OCN; the bone in senile osteoporosis, and to explore a relative- histomorphology analysis results indicated that ly more secure and effective way to prevent and LLLI could increase BFR and mineral apposition treat osteoporosis. rate (MAR), increase the number of osteoblasts MATERIALS AND METHODS: Sprague-Daw- and decrease the number of adipocytes in the ley (SD) male rats at different age stages (4 bone marrow in the old group.
    [Show full text]
  • Treatment of Postmenopausal Osteoporosis
    OSTEOPOROSIS IV Osteoporosis IV Treatment of postmenopausal osteoporosis Pierre D Delmas The aim of treatment of postmenopausal osteoporosis is to reduce the frequency of vertebral and non-vertebral fractures (especially at the hip), which are responsible for morbidity associated with the disease. Results of large placebo controlled trials have shown that alendronate, raloxifene, risedronate, the 1-34 fragment of parathyroid hormone, and nasal calcitonin, greatly reduce the risk of vertebral fractures. Furthermore, a large reduction of non-vertebral fractures has been shown for alendronate, risedronate, and the 1-34 fragment of parathyroid hormone. Calcium and vitamin D supplementation is not sufficient to treat individuals with osteoporosis but is useful, especially in elderly women in care homes. Hormone replacement therapy remains a valuable option for the prevention of osteoporosis in early postmenopausal women. Choice of treatment depends on age, the presence or absence of prevalent fractures, especially at the spine, and the degree of bone mineral density measured at the spine and hip. Non-pharmacological interventions include adequate calcium intake and diet, selected exercise programmes, reduction of other risk factors for osteoporotic fractures, and reduction of the risk of falls in elderly individuals. Osteoporosis is a worldwide health issue, with a high form of dairy products is as effective as calcium prevalence of disease not only in western countries but also supplements, supplements are necessary in most countries in Asia and Latin America. Of various fragility fractures, to achieve an adequate calcium intake. Calcium slows the which represent the major complication of the disease, rate of bone loss, especially in elderly women and in those vertebral and hip fractures are associated with pronounced with a low calcium intake.
    [Show full text]
  • Generalized Osteoporosis Inold
    Ann Rheum Dis: first published as 10.1136/ard.6.3.146 on 1 January 1947. Downloaded from GENERALIZED OSTEOPOROSIS IN OLD AGE BY C. M. KESSON, NOAH MORRIS*, and A. McCUTCHEON From the University Medical Clinic, Stobhill Hospital and the Department of Materia Medicq and Therapeutics, University ofGlasgow It is well known that frequently the bones become rarefied in old age and it is commonly believed that this rarefaction or osteoporosis is a physiological process. Generalized osteoporosis, however, occurs in a considerable proportion of the population long before old age is reached. In the pre-senile group many factors have been held responsible for the thinning of bones, and it seems possible that they may also account for osteoporosis in the aged. Attention was drawn to the sulbject of senile osteoporosis by Schmorl (1931), who studied the anatomy of the condition, and more recently by Meulengracht and Meyer (1936), who suggested that the main factor in the origin of the condition was long-standing calcium deficiency. This attractive hypothesis has received copyright. considerable support from Leitch (1936-37), Owen (1939), and Owen and others (1939). If this view is correct, senile osteoporosis must be included among the disorders of calcium metabolism, attention must be paid to the dietary require- ments of old folk, and the possibility considered of calcium metabolism in middle and old age differing from that of younger adults. Hyperparathyroidism (Hunter, 1929) and pituitary basophilism (Frey- 1930), hyperthyroidism (Aub and others, http://ard.bmj.com/ berg and Grant, 1936) have been found to cause generalized osteoporosis at all ages, but it is unlikely that dysfunction of these endocrine glands is responsible for osseous rarefaction in the old.
    [Show full text]
  • Prostaglandins and Bone: Potential Risks and Benefits Related to the Use of Nonsteroidal Anti-Inflammatory Drugs in Clinical Dentistry
    247 Journal of Oral Science, Vol. 50, No. 3, 247-252, 2008 Review Prostaglandins and bone: potential risks and benefits related to the use of nonsteroidal anti-inflammatory drugs in clinical dentistry Ricardo N. Fracon, Juliana M. Teófilo, Rafaela B. Satin and Teresa Lamano Department of Morphology, Stomatology and Physiology, Dentistry School of Ribeirão Preto, University of São Paulo, Brazil (Received 14 December 2007 and accepted 6 June 2008) Abstract: In the skeleton, prostaglandins, mainly prolonged treatment with NSAIDs, and which drug PGE2 produced by osteoblasts under COX-2 types are less harmful. (J. Oral Sci. 50, 247-252, 2008) stimulation, play either a stimulatory or an inhibitory role in bone metabolism, depending on the physiological Keywords: bone; prostaglandins; COX-1; COX-2; or pathological conditions. The anabolic effect occurs nonsteroidal anti-inflammatory drugs; largely in response to mechanical forces and in bone NSAIDs. fracture healing, whereas PGE2-mediated resorption contributes significantly to bone loss in inflammatory diseases and in response to prolonged immobilization. Introduction Many reports have shown that conventional The cyclooxygenase enzymes COX-1 and COX-2 nonsteroidal anti-inflammatory drugs (NSAIDs) may catalyze the conversion of arachidonic acid to prosta- delay fracture healing and negatively interfere with glandins (PGs). COX-1 is a constitutive enzyme normally spinal fusion in both humans and other animals, expressed in a variety of tissues and organs, leading to whereas the alleged inhibitory effects of COX-2-selective formation of PGs with physiological functions, such as NSAIDs still lacks experimental and clinical evidence. protection of gastrointestinal mucosa, control of renal Pertaining to clinical dentistry, recent studies have blood flow and homeostasis.
    [Show full text]
  • Senile Osteoporosis Is Associated with Disc Degeneration
    556 Editorial Senile osteoporosis is associated with disc degeneration Yì Xiáng J. Wáng Department of Imaging and Interventional Radiology, Faculty of Medicine, The Chinese University of Hong Kong, New Territories, Hong Kong, China Correspondence to: Dr. Yì Xiáng J. Wáng. Department of Imaging and Interventional Radiology, Faculty of Medicine, The Chinese University of Hong Kong, New Territories, Hong Kong, China. Email: [email protected]. Submitted Jul 10, 2018. Accepted for publication Jul 16, 2018. doi: 10.21037/qims.2018.07.04 View this article at: http://dx.doi.org/10.21037/qims.2018.07.04 Osteoporosis and disc degeneration of the spine are thereof, less likely be graded as having disc degeneration. common conditions that primarily affect the elderly with Another methodological issue is where and how to significant impact on the quality of life. A number of measure BMD. The prevalence of disc degeneration and studies reported that higher lumbar spine bone mineral facet arthrosis increases with aging, such that by 60 years of density (BMD) was associated with disc degeneration age, 60–80% of people have osteophytosis, disc narrowing, (1-5). However, other studies reported that osteoporotic and/or facet joint arthrosis (16). Degenerative changes patients have more severe disc degeneration (6,7). Some lead to artificially higher DAX-based areal lumbar BMD authors suggest that osteoporosis would possibly delay disc measurement due to marginal osteophytosis, trabecular degeneration because of an increase in intradiscal nutrient thickening, subchondral sclerosis, and facet joint arthrosis diffusion and a decreased endplate resistance and decreased (17,18). Narrowed disc spaces can lead to a higher areal intradiscal strain due to the low quality of the bone (8,9).
    [Show full text]