CC BY
17
UDC 616.74-007.23:616.71-001.5:616.8-009.1(048.8) https://doi.Org/10.26641/2307-0404.2021.2.234637
V.V. Povoroznyuk, the association of sarcopenia
KV. Dedukh and osteoporosis and their role
MA Bystrytska, in falls and fractures
N.I. Dzerovych,
V.S. Shapovalov
D.F. Chebotarev Institute of Gerontology of the National Academy of Medical Sciences of Ukraine
Vyshhorodska str., 67, Kyiv, 04111, Ukraine
e-mail: ig@geront.kiev.ua
Kyiv City Clinical Emergency Hospital
Bratyslavska str., 3, Kyiv, 02660, Ukraine
e-mail: bsmp@health.kiev.ua
ДУ «1нститут геронтологи iM. Д. Ф. Чеботарьова НАМН Украши»
(дир. - академк НАМН Укра'ши, д. мед. н., проф. В. В. Безруков)
вул. Вишгородська, 67, Ки'в, 04114, Украша
Кшвська MicbKa mmi4Ha лiкарнi швидкоi медичноi допомоги
вiддiлення нейрохiрургii
(голов. лжар - к. мед. н. О.А. Ткаченко)
вул. Братиславська, 3, Ки'в, 02660, Украша
Цитування: Медичш перспективы. 2021. Т. 26, № 2. С. 111-119 Cited: Medicni perspektivi. 2021;26(2):111-119
Key words: sarcopenia, osteosarcopenia, prevalence, metabolic disorders, falls, fractures
Ключовi слова: саркопетя, остеосаркопеня, поширетсть, метаболiчнi порушення, падтня, переломи
Ключевые слова: саркопения, остеосаркопения, распространенность, метаболические нарушения, падения,
переломы
Abstract. The association of sarcopenia and osteoporosis and their role in falls and fractures (literature review). Povoroznyuk V.V., Dedukh N.V., Bystrytska M.A., Dzerovych N.I., Shapovalov V.S. The progressive and generalized loss of skeletal muscle mass and strength leads to sarcopenia in elderly people. A new geriatric syndrome has been revealed - osteosarcopenia (osteosarcoporosis), which combines low bone mineral density with reduced muscle mass, strength and functional activity. The review presents data on the peculiarities of manifestation of these syndromes, the mechanisms of which are multifactorial and continue to be investigated. They are associated with genetic factors, lifestyle - lack of physical activity and malnutrition. The pathogenesis of sarcopenia involves mechanisms of chronic inflammation, changes in endocrine function, disturbance of neuromuscular connections and low reparation level. Sarcopenia correlates with low quality of life, disability, and death. The review analyzes the prevalence of sarcopenia which increases with age. However, there are conflicting results in the populations, which may be related to different clinical conditions, patient area, lifestyle and the use of different assessment criteria. The analysis of sarcopenia prevalence in men and women showed ambiguous results related to the studied population, involvement of different age groups ofpatients, different evaluation methods. Metabolic disorders in muscular and bone tissues were summarized on the basis of the analysis of the cross-influence of regulatory factors and metabolism products of these tissues; a close metabolic and functional association between them was shown. Fat infiltration of atrophied muscles and bone marrow is common in patients with sarcopenia and osteosarcoporosis, which affects muscle and bone tissue. Lipotoxicity and local inflammation stimulate the biosynthesis of pro-inflammatory cytokines. Literature analysis has shown controversial data on the association of sarcopenia and osteosarcopenia with falls and fractures, but based on meta-analysis data, which include an extensive body of information, it should be noted that individuals with sarcopenia and osteosarcopenia are more at risk of falls and fractures and require special special attention. The most common fracture in osteosarcopenia is the hip fracture.
Реферат. Поеднання саркопени та остеопорозу та ix роль при падшнях та переломах (огляд лтратури).
Поворознюк В.В., Дедух Н.В., Бистрицька М.А., Дзерович Н.1., Шаповалов В.С. Прогресуюча втрата скелетноi м'язовоi маси й сили призводить до розвитку саркопени в людей похилого вiку. Виявлено новий герiатричний синдром - остеосаркопешя (остеосаркопороз), в якому поеднуються низька мiнеральна щшьтсть кiстковоi тканини зi зниженою м'язовою масою, силою i функщональною активтстю. В оглядi представлен данi про особливостi проявiв цих синдромiв, багатофакторнi мехатзми котрих знаходяться в стадИ розширених до^джень. !х пов'язують з генетичними факторами та способом життя - не-достатньою фiзичною активнктю та неповноцiнним харчуванням. У патогенезi саркопенП залученi мехашзми хротчного запалення, змти ендокринноi функци, порушення нейром 'язових зв 'язюв i низький рiвень репарацп. Саркопетя т^но корелюе з низькою яюстю життя, iнвалiднiстю, смертю. В оглядi проаналiзовано показники поширеностi саркопенП, яю збыьшуються з вком. Однаку рiзних популяцiях отримаш суперечливi результати, ят можуть бути пов'язанi з рiзноманiтними клiнiчними умовами, регiоном проживання пацiентiв, способом
21/ Том XXVI/ 2
111
життя i використанням рьзних критерИв оцтки. Анализ поширеностi саркопени в чоловтв i жток показав неоднозначш результати, зумовленi до^джуваною популящею, залученням пацieнтiв ргзних вкових груп i неоднаковими методами о^нки. Метаболiчнi порушення в м'язовт i юстковш тканинах узагальненi на основi анализу перехресного впливу регуляторних факторiв i продуктiв метабол1зму цих тканин, показано ткний метаболiчний та функцюнальний зв'язокмiж ними. У пацieнтiв 1з саркопетею й остеосаркопорозом поширена жирова iнфiльтрацiя атрофованих м ^в i юсткового мозку, що впливае на метаболизм м 'язовог i юстковог тканин. Лтотоксичтсть i мiсцеве запалення стимулюють бюсинтез прозапальних цитоютв. Анализ лiтератури показав суперечливi дан про асоцiацiю саркопени й остеосаркопенИ з падiннями i переломами, однак Трунтуючись на даних метааналЫв, як включають великий масив тформацИ, ^д зазначити, що особи з саркопенieю й остеосаркопенieю бшьш схильнi до ризику падть, переломiв i вимагають особливог уваги. Найбыьш тяжким переломом при остеосаркопени е перелом проксимального вiддiлу стегновог юстки.
I.H. Rosenberg first described sarcopenia as a loss of skeletal muscle mass with age [32]. In 2016, sarcopenia was included in the International Classification of Diseases (10th edition, code M62.84) [5, 13]. This pathology is characterized by progressive generalized skeletal muscle mass and strength loss, which is reflected in their function, manifested by general weakness, increased risk of falls, fractures, disability and increased mortality.
The diagnostic criteria for sarcopenia were proposed by the European Working Group on Sarcopenia (EGSOP) [36]. These include hand-grip dynamometry, gait speed and muscle mass. The most commonly used questionnaires for diagnosis are SarQol (Sarcopenia and Quality of Life) and SARC-F (Strength, Assistance with walking, Rise from a chair, Climb stairs and Falls).
Epidemiology
Prevalence. The number of older people around the world are steadily increasing and sarcopenia is the leading disease at this age, although it may also manifest itself at younger ages. Sarcopenia is considered to be a skeletal muscle pathology, including osteoporosis, and also develops with neoplasms, chronic obstructive pulmonary disease, chronic renal failure, etc.
The development of sarcopenia is facilitated by many factors affecting the loss of muscle mass and strength at any age, such as lack of physical activity, poor nutrition, endocrine system and metabolic disorders, chronic inflammation, as well as genetic factors [2]. With age, the biosynthesis of muscle proteins and regulatory factors decreases, which slows down reparative processes in muscle tissue.
The number of patients in Europe is expected to increase from 20 to 32.3 million by 2045 [39]. In the USA 12-14% of people have sarcopenia (about 50 million people) and a doubling of number of patients by 2050 is predicted. As reported in 2014 by of the European Working Group on Sarcopenia in Older People (EWGSOP) and International Working Group on Sarcopenia (IWGS) prevalence of sarco-penia was registered in 1-29% of those in community-dwelling populations of older adults, 14-
33% in long-term care institutions and 10% in the acute hospital-care population [28]. The prevalence of sarcopenia was 19.2% in males and 8.6% in females aged >65 [38]. Other studies have shown that sarcopenia prevalence was from 2% to 37% in communities [31, 41]. A high percentage of sar-copenia (32.8%), of which 68% were men, was found among people aged 70 years and living in communities. The disease was registered in 50% of people aged > 80 years [36].
Prevalence of sarcopenia among apparently healthy Ukrainian women, as shown for other populations, increases with age. Sarcopenia indicatots were 4.1% among 50-59 years old (y/|o), 3.7% - 6069 y/o, 18.4% - 70-79 y/o, 30.8% - 80-89 y/o [1]. In estimating the prevalence of sarcopenia in men and women, there are controversial results, which may be related to the studied population and different age groups [31].
Falls and fractures in sarcopenia. Sarcopenia also affects a person's tendency to fall, which in some cases ends in a fracture [3, 33]. An imbalance is a strong risk factor for falling. The ability to maintain balance requires the interaction of the motor (muscular), nervous and sensory systems, the functions of which decrease with age. In a cross-sectional study in Australia in 2015 involving 680 elderly people with sarcopenia, falls were recorded in 40% of individuals [27]. Meta-analysis data, which included 2,771 literature sources are presented [33]. Individuals with sarcopenia were found to have a higher risk of falling (OR 1.60; 95% CI 1.37-1.86, P<0.001, I2=34%) and fractures (OR 1.84; 95% CI 1.30-2.62, P=0.001, I2=91%) compared to patients without sarcopenia.
The ilSIRENTE study evaluated the relationship between sarcopenia and 2-year risk of falling among 260 persons aged 80 and over [34]. Sarcopenia was found in 66 participants (25.4%), 18 of whom (27.3%) reported falling incidents during the 2-year observation period. It was found that persons with sarcopenia were more than three times prone to falling.
A survey of a group of 2000 men in the community aged >65 found that sarcopenia was
associated with an increased risk of fractures (OR 1.87; 95% CI 1.26-2.79) regardless of bone mineral density (BMD) and other clinical risk factors [45]. Another study based on meta-analysis has shown that sarcopenia is a risk factor for falling among older people living in communities (OR=1.52, CI: 1.32-1.77) [14].
However, there are sporadic studies that do not show a connection between sarcopenia, falls and fractures. In a study of 498 adult men and women, a weak association between sarcopenia and falls was shown and no connection with fractures was found [37]. Another study also showed no correlation between sarcopenia and fracture in the distal end of the forearm bones, but found a strong correlation with BMD [20].
That is, sarcopenia's association with falls is presented in a variety of ways, but based on meta-analyses that include a vast array of information, it should be noted that people with sarcopenia are more likely to fall and fracture.
At the same time, the development of sarcopenia may also be associated with a previous fracture. A review has been carried out on the PubMed and Cochrane databases to analyze and generalize data on the prevalence of sarcopenia in low-energy fracture patients and to identify fracture risk factors in sarcopenia patients [43]. The prevalence of sarcopenia after fracture ranged from 12.4% to 95% in men and from 18.3% to 64% in women. Two studies have shown that sarcopenia was a significant risk factor for low-trauma fracture at low BMD, but only in men. The authors believe that there is an urgent need for further research into the relationship between sarcopenia and low-energy fracture risk, in order to better understand its pathophysiological mechanisms.
In a Spanish study, sarcopenia incidence in patients with low-energy hip fracture was 17.1% (12.4% in men, 18.3% in women) [30]. The prevalence of sarcopenia in patients with hip fracture in the Chinese population was 73.6% in males and 67.7% in females, and 20.8% and 12.4%, respectively, as defined by the Asian Sarcopenia Working Group [29]. In the Taiwanese population of 139 patients with hip fracture, 70 (50.3%) had sarcopenia [40]. Sarcopenia has also been associated with an increased risk of vertebral fractures [11]. These data suggest that fractures in old age can be considered a risk factor for sarcopenia.
In addition, there is a study showing that after proximal femur fractures, older patients with sar-copenia need more blood for transfusion during the perioperative period and longer postoperative hospitalization [12].
Mechanisms of the interrelation of the bone and muscular systems
The bone and muscular systems are closely linked. Bone remodeling is not only dependent on the gravitational load, but also on the functional activity of the muscles and the close metabolic connection between the two systems. The concept of "musculoskeletal unit" has been developed, which is based on linear relationships at different ages between BMD and muscle mass, and the cross-influence of these tissues.
An association study (GWAS) has shown that some genes are associated with both sarcopenia and osteoporosis. These include polymorphisms of genes encoding myostatin (MSTN), a-actinin 3 (ACTN3), glycine-N-acyltransferase (GLYAT), and methyl-transferase-like protein 21C (METTL21C), coacti-vator of 1-alpha receptor, proliferator-activated by peroxisome proliferators, gamma (PGC-1a) and myocyte enhancer factor 2C (MEF-2C) [18, 23].
Myokines, humoral cytokines and growth factors expressed by skeletal muscles affect bone metabolism. Among them are myostatin, insulin-like growth factor-1 (IGF-1), fibroblast growth factor-2 (FGF-2), interleukins (1, 6, 15), osteoglycin, osteonectin, the family of proteins FAM5C, irisin, transmembrane protein 119 (Tmem 119), matrix metal-loproteinase-2, activin, follistatin, monocyte chemo-attractant protein (MCP)-1, transforming growth factor-p (TGF-P), bone morphogenetic proteins (BMPs), ciliary neurotrophic factor (CNTF) and others. The functions of many of them are not fully understood [21, 22].
Myostatin plays an important role in bone remodeling. It reduces bone formation and stimulates resorption, influencing the proliferation of osteoclasts by stimulating the expression of genes producing the RANKL by osteoblasts, receptor in-tegrin aVp3, dendrocyte expressed seven transmembrane protein (DCSTAMP) and calcitonin receptor.
However, despite the established pathways of myokines' influence on bone metabolism, this direction requires further research, which will contribute to accurate diagnostics and development of methods for treatment of muscle and bone diseases, such as sarcopenia and osteoporosis.
Sarcopenia increases the expression of pro-inflammatory TNF-a and C-reactive protein molecules that directly or indirectly affect muscu-loskeletal metabolism [44]. The state of muscle tissue is affected by mitochondrial dysfunction observed in sarcopenia, associated with increased apoptosis, which is accompanied by low reparative ability [35].
21/ Том XXVI/ 2
113
Growth hormone, sex hormones, and pathological conditions such as excess glucocorticoids and diabetes affect both muscles and bones [21].
There is also a reverse pathway of the influence of bone tissue on muscle tissue through the secretion of osteoblasts and osteocytes of osteokines, among which: prostaglandin E2, sclerostin and osteocalcin [21]. Osteocalcin stimulates the proliferation of P-cells of the pancreas, which secrete insulin, affecting the metabolism of muscle tissue. Myoblasts proliferation is also affected by the secretion of vascular endothelial growth factor (VEGF) by mesenchymal stromal cells of the bone marrow. Protein of the signaling pathway Wnt-3a expressed by bone cells also affects muscle function, but this pathway has not been sufficiently studied.
The effect of vitamin D deficiency on muscle and bone tissue has been studied and evaluated, which is accompanied not only by a decrease in BMD, but also by a decrease in muscle strength, lengthening the relaxation phase of muscle contraction. Vitamin D affects muscle and bone cells both directly through receptor (VDR) and indirectly, affecting calcium homeostasis, phosphate and parathyroid hormone (PTH) secretion [7].
Closely related homeostasis of bone, muscle and adipose tissue is supported through neuro-humoral connections. In patients with sarcopenia and osteoporosis, fat infiltration of atrophied muscles and bone marrow is widespread, affecting muscle and bone tissue. Lipotoxicity and local inflammation stimulate biosynthesis of proinflammatory cytokines, among which are interleukin-6 (IL-6) and tumor necrosis factor alpha (TNF-a) [18]. In clinical practice, sarcopenia in combination with osteopenia/osteoporosis and other disorders of body composition (high fat mass) are quite common. These states are defined as sarcopenic obesity or osteosarcopenic obesity [4].
Osteosarcopenia
Given the close relationship and commonality of osteoporosis and sarcopenia pathogenesis, the term "osteosarcopenia" or "sarcoporosis" is now widely used [9]. Osteosarcopenia has been described as a new geriatric syndrome that combines low BMD with reduced muscle mass, strength and functional activity [16, 23]. No specific markers of this pathology have been revealed, however, it has been established that such patients have lower levels of testosterone, vitamin D and hemoglobin in comparison with isolated pathology - osteoporosis or sarcopenia [2]. The development of osteosarcopenia is influenced by endocrine diseases, alimentary insufficiency, obesity and corticosteroid intake.
In a study published in 2019, which included 3,334 elderly people, it was demonstrated that
individuals with a confirmed sarcopenia diagnosis had lower BMD rates and bone architecture disorders in various anatomical skeletal areas compared to those without sarcopenia [6].
The prevalence of osteosarcopenia in the elderly living in community is 4.7% in Japan, 28% in Germany, ranging from 7% to 13% in China, with the highest rates of 40% in Australia and 34% in Iran [14, 19, 26]. Osteosarcopenia incidence increases with age, in men it ranges from 14.3% (60-64 years) to 59.4% (> 75 years), in women it is 20.3% (60-64 years) to 48.3% (> 75 years) [24].
However, in another study, higher rates of osteo-sarcopenia were recorded in women, ranging from 2.5 to 82.6%, compared with 16.4 to 32.0% for men [15].
The prevalence of sarcopenia depended on the criteria used to establish the diagnosis. Cases of sarcopenia (92 patients, mean age 66±10 years, 90% of women) according to core muscle index (CMI) criteria were found in 65% of patients (9% had sarcopenia, 56% had osteopenia), only 22% had osteopenia/osteoporosis, 13% - without these pathologies [8]. In terms of handgrip strength, sarcopenia was found in 60% of individuals, in gait speed -45% and by SARC-F score (A Simple Questionnaire to Rapidly Diagnose Sarcopenia) - 40%. Osteo-sarcopenia according to handgrip strength was found in 51%, gait speed - 34% and SARC-F score - 32%.
According to X-ray bone densitometry and skeletal muscle index (skeletal muscle mass divided by height in meters, squared, SMI), sarcopenia was found in persons with normal BMD in 40%, with osteopenia - 64%, with osteoporosis - 76%. When comparing the frequency of pathology by sex, gender-specific features were identified, sarcopenia was recorded in 69% of women and 33% of men (p=0.034). Patients with osteosarcopenia and sarcopenia had lower body weight indices, skeletal muscle mass and appendicular mass (limb muscle mass) as well as skeletal muscle index compared to patients with osteopenia/osteoporosis or without this pathology [8].
Among the 2,353 individuals living in the community, risk factors associated with osteosarcopenia included older age (men: 14.3% (60-64 years) to 59.4% (>75 years); women: 20.3% (60-64 years) to 48.3% (>75 years); physical inactivity (cumulatively men and women (OR): 0.64, 95%, CI 0.46-0.88), low body mass index (OR: males: 0.84, 95%, CI 0.81-0.88; females: 0.77, 95%, CI 0.74-0.80) and higher fat mass (males: 1.46, 95%, CI 1.11-1.92; females: 2.25, 95%, CI 1.71-2.95) [24].
The data are controversial with respect to the risk of fall and fracture in osteoporosis (compared to sarcopenia and osteoporosis). In a prospective cohort study the Osteoporotic Fractures in Men (MrOs),
which lasted from 2001 to 2013 and included 2,000 individuals (>65 years), it was found that men with osteoporosis have a 3.5 times greater risk of fractures than men with sarcopenia or only osteoporosis [45].
A study in Australia (253 individuals, 77% of whom were 77.9±0.42 years old women) found that the risk of fall (ODs: 2.83-3.63; p<0.05) and fracture (ODs: 3.86-4.38; P < 0.05) was significantly higher in osteosarcopenia patients than in those without this pathology [42]. The combination of osteoporosis and sarcopenia resulted in a significant increase in the risk of fracture (OR 3.49, 95% CI 1.76-6.90) in comparison with persons with normal BMD and without sarcopenia [45].
Osteosarcopenia was high - 5 to 37% in older people (>65 years) living in communities. Sar-copenia following low-trauma fractures was found in 46% of patients, of whom 17.1-96.3% had hip fractures [24]. The hip fracture is associated with increased mortality in osteosarcopenia patients [25].
In the comparative analysis of the risk of fractures and falls in 1575 men with osteosarcopenia aged over 70 years, no distinctive features were revealed in comparison with osteopenia/osteoporosis and sarcopenia groups [10]. The participants were contacted for 2 years, and for radiologically confirmed fracture incidents - every 4 months for 6±2 years.
The relationship of osteosarcopenia with serum PTH levels and falls was found. Of the 400 patients
surveyed, 24% had high PTH levels with normal adjusted calcium levels. These individuals reported more falls per year and had low levels of muscle strength, gait rate and BMD [17].
When osteoporosis and sarcopenia are combined, different results concerning the risk of falls and fractures are obtained. These data indicate a need for in-depth research in this area.
Thus, sarcopenia is regarded as a separate noso-logic form presented in the International Classification of Diseases 10 (ICD-10) as a syndrome that may manifest itself as a primary or secondary condition. The manifestation of sarcopenia is associated with loss of muscle mass, strength and is combined with an increased risk of falls and fractures. In turn, fractures may be a pathogenetic factor in sarcopenia. Numerous signaling pathways leading to disturbance of metabolism and muscle structure have been described and the close metabolic and functional association between muscle and bone tissue has been demonstrated. The concept of osteo-sarcopenia as a new geriatric syndrome has been developed. Osteosarcopenia is widespread in various populations and is associated with serious health consequences in terms of quality of life: general weakness, increased risk of falls, fractures and mortality.
Conflict of interests. The authors declare no conflict of interest.
references
1. Povoroznyuk V, Dzerovych N. [Sarcopenia (literature review)]. Journal of the NAMSU. 2019;25(3):321-31. Ukrainian.
2. Mokrysheva NG, Krupinova JA, Volodiche-va LV, Mirnaya SS, Melnichenko GA. [A view at sarcopenia by endocrinologist]. Obesity and Metabolism. 2018;1(3):21-27. Russian.
doi: https://doi.org/10.14341/OMET9792
3. Safonova YA. [Sarcopenia risk factor for falls and fractures]. The Clinician. 2019;13(3-4):22-28. Russian. doi: https://doi.org/10.17650/1818-8338-2019-13-3-4-22-28
4. Shostak NA, Muradyantz AA, Kondrashov AA. [Sarcopenia and overlapping syndromes: their value in clinical practice]. The Clinician. 2016;10(3):10-14. Russian. doi: https://doi.org/10.17650/1818-8338-2016-10-3-10-14
5. Anker SD, Morley JE, von Haehling S. Welcome to the ICD-10 code for sarcopenia. J Cachexia Sarcopenia Muscle. 2016;7(5):512-4.
doi: https://doi.org/10.1002/jcsm. 12147
6. Scott D, Johansson J, McMillan LB, Ebeling PR, Nordstrom P, Nordstrom A. Associations of Sarcopenia and Its Components with Bone Structure and Incident Falls in Swedish Older Adults. Calcif Tissue Int [Internet]. 2019;105(1):26-36.
doi: http://doi.org/10.1007/s00223-019-00540-1.
7. Kim J, Lee Y, Kye S, Chung YS, Lee O. Association of serum vitamin D with osteosarcopenic obesity: Korea National Health and Nutrition Examination Survey 20082010. J Cachexia Sarcopenia Muscle. 2017;8(2):259-66. doi: https://doi.org/ 10.1002/jcsm.12154
8. Intriago M, Maldonado G, Guerrero R, Messina OD, Rios C. Bone Mass Loss and Sarcopenia in Ecuadorian Patients. J Aging Res. 2020;2020, Article ID 1072675. doi: https://doi.org/10.1155/2020/1072675
9. Cedeno-Veloz B, Lopez-Doriga Bonnardeauxa P, Duque G. Osteosarcopenia: A narrative review. Revista Espanola de Geriatria y Gerontologia. Ediciones Doyma, S.L.; 2019;54:103-8.
doi : https://doi.org/10.1016/j.regg.2018.09.010
10. Scott D, Seibel M, Cumming R, Naganathan V, Blyth F, Le Couteur DG, et al. Does combined osteope-nia/osteoporosis and sarcopenia confer greater risk of falls and fracture than either condition alone in older men? The concord health and ageing in men project. Journals Gerontol - Ser A Biol Sci Med Sci. 2019;74(6):827-34. DOI: https://doi.org/10.1093/gerona/gly162
11. Anand A, Shetty AP, Renjith KR, Sri Vijay Anand KS, Kanna RM, Rajasekaran S. Does Sarcopenia increase the risk for fresh vertebral fragility fractures?: A
21/ Том XXVI/ 2
115
case-control study. Asian Spine J. 2020;14(1):17-24. DOI: https://doi.org/10.31616/asj.2019.0049
12. Chang C Di, Wu JS, Mhuircheartaigh JN, Hoch-man MG, Rodriguez EK, Appleton PT, et al. Effect of sarcopenia on clinical and surgical outcome in elderly patients with proximal femur fractures. Skeletal Radiol. 2018 Jun 1;47(6):771-7.
doi: https://doi.org/10.1007/ s00256-017-2848-6
13. Falcon LJ, Harris-Love MO. Sarcopenia and the New ICD-10-CM Code: Screening, Staging, and Diagnosis Considerations. Fed Pract. 2017;34(7):24-32. PMCID: PMC5576154.
14. Zhang X, Huang P, Dou Q, Wang C, Zhang W, Yang Y, et al. Falls among older adults with sarcopenia dwelling in nursing home or community: A meta-analysis. Clin Nutr. 2020;39(1):33-9. doi: https://doi.org/10.1016/j.clnu.2019.01.002
15. Simmonds SJ, Syddall HE, Westbury LD, Dodds RM, Cooper C, Aihie Sayer A. Grip strength among community-dwelling older people predicts hospital admission during the following decade. Age Ageing. 2015;44(6):954-9.
doi: https://doi.org/10.1093/ageing/afv146
16. Hassan EB, Duque G. Osteosarcopenia: A new geriatric syndrome. Aust Fam Physician. 2017;46(11):849-53. PMID: 29101922.
17. Suriyaarachchi P, Gomez F, Curcio CL, Boersma D, Murthy L, Grill V, et al. High parathyroid hormone levels are associated with osteosarcopenia in older individuals with a history of falling. Maturitas. 2018 Decem.;113:21-25.
doi: https://doi.org/10.1016/j.maturitas.2018.04.006
18. Hirschfeld HP, Kinsella R, Duque G. Osteosar-copenia: where bone, muscle, and fat collide. Osteoporos Int. 2017;28(10):2781-90.
doi: https://doi.org/10.1007/s00198-017-4151-8
19. Yoshimura N, Muraki S, Oka H, Iidaka T, Kodama R, Kawaguchi H, et al. Is osteoporosis a predictor for future sarcopenia or vice versa? Four-year observations between the second and third ROAD study surveys. Osteoporos Int. 2017;28(1):189-99. doi: http://dx.doi.org/10.1007/s00198-016-3823-0
20. Lee J-K, Yoon B-H, Oh CH, Kim JG, Han S-H. Is Sarcopenia a Potential Risk Factor for Distal Radius Fracture? Analysis Using Propensity Score Matching. J Bone Metab. 2018;25(2):99.
doi: https://doi.org/10.11005/jbm.2018.25.2.99
21. Kawao N, Kaji H. Interactions between muscle tissues and bone metabolism. J Cell Biochem. 2015;116(5):687-95.
doi: https://doi.org/10.1002/jcb.25040
22. Kaji H. Effects of myokines on bone. Bonekey Rep. 2016;5(July):1-6.
doi: https://doi.org/ 10.1038/bonekey.2016.48
23. Kirk B, Al Saedi A, Duque G. Osteosarcopenia: A case of geroscience. Aging Med. 2019;2(3):147-56. doi: https://doi.org/10.1002/agm2.12080
24. Kirk B, Zanker J, Duque G. Osteosarcopenia: epidemiology, diagnosis, and treatment - facts and numbers. J Cachexia Sarcopenia Muscle. 2020;11(3):609-18. doi: https://doi.org/10.1002/jcsm.12567
25. Yoo J Il, Kim H, Ha YC, Kwon H Bin, Koo KH. Osteosarcopenia in patients with hip fracture is related with high mortality. J Korean Med Sci. 2018;33(4):1-9. doi: https://doi.org/10.3346/jkms.2018.33.e27
26. Drey M, Sieber CC, Bertsch T, Bauer JM, Schmi-dmaier R. The FiAT intervention group. Osteosarcopenia is more than sarcopenia and osteopenia alone. Aging Clin Exp Res. 2016;28(5):895-9.
doi: https://doi.org/10.1007/s40520-015-0494-1
27. Huo YR, Suriyaarachchi P, Gomez F, Curcio CL, Boersma D, Muir SW, et al. Phenotype of Osteosarco-penia in Older Individuals With a History of Falling. J Am Med Dir Assoc. 2015;16(4):290-5. doi: https://doi.org/10.1016/jjamda.2014.10.018
28. Cruz-Jentoft AJ, Landi F, Schneider SM, Zùniga C, Arai H, Boirie Y, et al. Prevalence of and interventions for sarcopenia in ageing adults: A systematic review. Report of the International Sarcopenia Initiative (EWGSOP and IWGS). Age Ageing. 2014 Nov 1;43(6):48-759. doi: https://doi.org/10.1093/ageing/afu115
29. Ho AWH, Lee MML, Chan EWC, Ng HMY, Lee CW, Ng WS, et al. Prevalence of pre-sarcopenia and sarcopenia in Hong Kong chinese geriatric patients with hip fracture and its correlation with different factors. Hong Kong Med J. 2016;22(1):23-29. doi: https://doi.org/10.12809/hkmj154570
30. Gonzalez-Montalvo JI, Alarcon T, Gotor P, Queipo R, Velasco R, Hoyos R, et al. Prevalence of sarco-penia in acute hip fracture patients and its influence on short-term clinical outcome. Geriatr Gerontol Int. 2016;16(9):1021-7. doi: https://doi.org/10.1111/ggi.12590
31. Shafiee G, Keshtkar A, Soltani A, Ahadi Z, La-rijani B, Heshmat R. Prevalence of sarcopenia in the world: A systematic review and meta-analysis of general population studies. J Diabetes Metab Disord. 2017;16(1):1-10. doi: https://doi.org/10.1016/jjamda.2019.09.005
32. Rosenberg IH. Symposium: Sarcopenia: Diagnosis and Mechanisms Sarcopenia: Origins and Clinical Relevance 1. J Nutr. 1997;127:990-1.
33. Yeung SSY, Reijnierse EM, Pham VK, Trappenburg MC, Lim WK, Meskers CGM, et al. Sarcopenia and its association with falls and fractures in older adults: A systematic review and meta-analysis. J Cachexia Sarcopenia Muscle. 2019;10(3):485-500. doi: https://doi.org/10.1002/jcsm. 12411
34. Landi F, Liperoti R, Russo A, Giovannini S, To-sato M, Capoluongo E, et al. Sarcopenia as a risk factor for falls in elderly individuals: Results from the ilSIRENTE study. Clin Nutr. 2012;31(5):652-8. doi: https://doi.org/10.1016/j.clnu.2012.02.007
35. Lo JH, U KP, Yiu T, Ong MT, Lee WY. Sar-copenia: Current treatments and new regenerative therapeutic approaches. J Orthop Transl. 2020;23:38-52. doi: https://doi.org/10.1016/j.jot.2020.04.002
36. Cruz-Jentoft AJ, Bahat G, Bauer J, Boirie Y, Bruyère O, Cederholm T, et al. Sarcopenia: Revised European consensus on definition and diagnosis. Age and Ageing. Oxford University Press; 2019;48:16-31. doi: https://doi.org/10.1093/ageing/afy169
37. Schaap LA, Van Schoor NM, Lips P, Visser M. Associations of sarcopenia definitions, and their
components, with the incidence of recurrent falling and fractures: The longitudinal aging study Amsterdam. Journals Gerontol - Ser A Biol Sci Med Sci. 2018;73(9):1199-204. doi: https://doi.org/10.1093/gerona/glx245
38. Du Y, Wang X, Xie H, Zheng S, Wu Xi, Zhu X, Zhang X, Xue S, Li H, Hong W, Tang W, Chen M, Cheng Q, Sun J. Sex differences in the prevalence and adverse outcomes of sarcopenia and sarcopenic obesity in community dwelling elderly in East China using the AWGS criteria. BMC Endocr Disord. 2019;19(1):109. doi: https://doi.org/10.1186/s12902-019-0432-x
39. Ethgen O, Beaudart C, Buckinx F, Bruyère O, Reginster JY. The Future Prevalence of Sarcopenia in Europe: A Claim for Public Health Action. Calcif Tissue Int. 2017;100(3):229-34.
doi: https://doi.org/doi: 10.1007/s00223-016-0220-9
40. Chen YP, Wong PK, Tsai MJ, Chang WC, Hsieh TS, Leu TH, et al. The high prevalence of sarco-penia and its associated outcomes following hip surgery in Taiwanese geriatric patients with a hip fracture. J Formos Med Assoc. 2020 Feb 24;S0929-6646(20)30041-3. doi: https://doi.org/10.1016/jjfma.2020.02.004
41. Reijnierse EM, Trappenburg MC, Leter MJ, Blauw GJ, Sipilä S, Sillanpää E, et al. The Impact of
Different Diagnostic Criteria on the Prevalence of Sar-copenia in Healthy Elderly Participants and Geriatric Outpatients. Gerontology. 2015;61(6):491-6. doi: https://doi.org/doi: 10.1159/000377699
42. Sepùlveda-Loyola W, Phu S, Bani Hassan E, Brennan-Olsen SL, Zanker J, Vogrin S, et al. The Joint Occurrence of Osteoporosis and Sarcopenia (Osteosar-copenia): Definitions and Characteristics. J Am Med Dir Assoc. 2020;21(2):220-5.
doi: https://doi.org/10.1016/jjamda.2019.09.005
43. Wong RMY, Wong H, Zhang N, Chow SKH, Chau WW, Wang J, et al. The relationship between sarcopenia and fragility fracture - a systematic review. Osteoporos Int. 2019;30(3):541-53.
doi: https://doi.org/10.1007/s00198-018-04828-0
44. Wilson D, Jackson T, Sapey E, Lord JM. Frailty and sarcopenia: The potential role of an aged immune system. Ageing Res Rev. 2017;36:1-10. doi: http://dx.doi.org/10.1016/j.arr.2017.01.006
45. Yu R, Leung J, Woo J. Incremental predictive value of sarcopenia for incident fracture in an elderly chinese cohort: Results from the osteoporotic fractures in men (MrOs) study. J Am Med Dir Assoc. 2014;15(8):551-8. doi: http://dx.doi.org/10.1016/jjamda.2014.02.005
список л1тератури
1. Поворознюк В. В. Дзерович Н. I. Саркопетя: огляд лггератури. Журнал НАМН Украши. 2019. Т. 25, № 3. P. 321-331.
2. Саркопения глазами эндокринолога / Н. Г. Мо-крышева и др., Ожирение и метаболизм. 2018. Т. 1, № 3. P. 21-27. DOI: https://doi.org/10.14341/OMET9792
3. Сафонова Ю. А. Саркопения как фактор риска падений и переломов. Клиницист. 2019. Т. 13, № 3-4. С. 22-28.
DOI: https://doi.org/10.17650/1818-8338-2019-13-3-4-22-28
4. Шостак Н. А., Мурадянц А. А., Кондратов А. А. Саркопения и перекрестные синдромы - значение в клинической практике. Клиницист. 2016. Т. 10. № 3. С. 10-14.
DOI: https://doi.org/10.17650/1818-8338-2016-10-3-10-14
5. Anker S. D., Morley J. E., von Haehling S. Welcome to the ICD-10 code for sarcopenia. J. Cachexia. Sarcopenia Muscle. 2016. Vol. 7, No. 5. P. 512-514. DOI: https://doi.org/10.1002/jcsm.12147
6. Associations of Sarcopenia and Its Components with Bone Structure and Incident Falls in Swedish Older Adults / D. Scott et al. Calcif. Tissue Int. 2019. Vol. 105, No. 1. P. 26-36.
DOI: https://doi.org/10.1007/s00223-019-00540-1
7. Association of serum vitamin D with osteosar-copenic obesity: Korea National Health and Nutrition Examination Survey 2008-2010 / J. Kim et al. Cachexia. Sarcopenia Muscle. 2017. Vol. 8, No. 2. P. 259-266. DOI: https://doi.org/10.1002/jcsm.12154
8. Bone Mass Loss and Sarcopenia in Ecuadorian Patients / M. Intriago et al. J. Aging Res. 2020. Vol. 2020. Article ID 1072675.
DOI: https://doi.org/10.1155/2020/1072675
9. Cedeno-Veloz B., Lopez-Doriga Bonnardeau-xa P., Duque G. Osteosarcopenia: A narrative review. Revista Espanola de Geriatria y Gerontologia. 2019. Vol. 54, No. 2. P. 103-108.
DOI: https://doi.org/10.1016/j.regg.2018.09.010
10. Does combined osteopenia/osteoporosis and sarcopenia confer greater risk of falls and fracture than either condition alone in older men? The concord health and ageing in men project / D. Scott et al. Journals Gerontol. Ser. A Biol. Sci. Med. Sci. 2019. Vol. 74, No. 6. P. 827-834.
DOI: https://doi.org/10.1093/gerona/gly162
11. Does Sarcopenia increase the risk for fresh vertebral fragility fractures?: A case-control study / A. Anand et al. Asian Spine J. 2020. Vol. 14, No. 1. P. 17-24. DOI: https://doi.org/10.31616/asj.2019.0049
12. Effect of sarcopenia on clinical and surgical outcome in elderly patients with proximal femur fractures / C. Di. Chang et al. Skeletal Radiol. 2018. Vol. 47, No. 6. P. 771-777.
DOI: https://doi.org/10.1007/ s00256-017-2848-6
13. Falcon L. J., Harris-Love M. O. Sarcopenia and the New ICD-10-CM Code: Screening, Staging, and Diagnosis Considerations. Fed. Pract. 2017. Vol. 34, No. 7. P. 24-32. PMCID: PMC5576154.
14. Falls among older adults with sarcopenia dwelling in nursing home or community: A meta-analysis / X. Zhang et al. Clin. Nutr. 2020. Vol. 39, No. 1. P. 33-39. DOI: https://doi.org/10.1016/j.clnu.2019.01.002
15. Grip strength among community-dwelling older people predicts hospital admission during the following decade / S. J. Simmonds et al. Age Ageing. 2015. Vol. 44, No. 6. P. 954-959. DOI: https://doi.org/10.1093/ageing/afv146
21/ Том XXVI/ 2
117
16. Hassan E. B., Duque G. Osteosarcopenia: A new geriatric syndrome. Aust. Fam. Physician. 2017. Vol. 46, No. 11. P. 849-853. PMID: 29101922.
17. High parathyroid hormone levels are associated with osteosarcopenia in older individuals with a history of falling / P. Suriyaarachchi et al. Maturitas. 2018. Dec. (Vol. 113). P. 21-25.
DOI: https://doi.org/10.1016Zj.maturitas.2018.04.006
18. Hirschfeld H. P., Kinsella R., Duque G. Os-teosarcopenia: where bone, muscle, and fat collide. Osteoporos. Int. 2017. Vol. 28, No. 10. P. 2781-2790. DOI: https://doi.org/10.1007/s00198-017-4151-8
19. Is osteoporosis a predictor for future sarcopenia or vice versa? Four-year observations between the second and third ROAD study surveys / N. Yoshimura et al. Osteoporos. Int. 2017. Vol. 28, No. 1. P. 189-199. DOI: https://doi.org/10.1007/s00198-016-3823-0
20. Is Sarcopenia a Potential Risk Factor for Distal Radius Fracture? Analysis Using Propensity Score Matching / J.-K. Lee et al. J. Bone Metab. 2018. Vol. 25, No. 2. P. 99. DOI: https://doi.org/10.11005/jbm.2018.25.2.99
21. Kawao N., Kaji H. Interactions between muscle tissues and bone metabolism. J. Cell. Biochem. 2015. Vol. 116, No. 5. P. 687-695.
DOI: https://doi.org/ 10.1002/jcb.25040
22. Kaji H. Effects of myokines on bone. Bonekey Rep. 2016. July (Vol. 5). P. 1-6.
DOI: https://doi.org/ 10.1038/bonekey.2016.48
23. Kirk B., Al Saedi A., Duque G. Osteosarcopenia: A case of geroscience. Aging Med. 2019. Vol. 2, No. 3. P. 147-156. DOI: https://doi.org/10.1002/agm2.12080
24. Kirk B., Zanker J., Duque G. Osteosarcopenia: epidemiology, diagnosis, and treatment—facts and numbers. J. Cachexia. Sarcopenia Muscle. 2020. Vol. 11, No. 3. P. 609-618.
DOI: https://doi.org/10.1002/jcsm.12567
25. Osteosarcopenia in patients with hip fracture is related with high mortality / J. I. Yoo et al. J. Korean Med. Sci. 2018. Vol. 33, No. 4. P. 1-9. DOI: https://doi.org/10.3346/jkms.2018.33.e27
26. Osteosarcopenia is more than sarcopenia and osteopenia alone / M. Drey et al. Aging Clin. Exp. Res. 2016. Vol. 28, No. 5. P. 895-899. DOI: https://doi.org/10.1007/s40520-015-0494-1.
27. Phenotype of Osteosarcopenia in Older Individuals With a History of Falling / Y. R. Huo et al. J. Am. Med. Dir. Assoc. 2015. Vol. 16, No. 4. P. 290-295. DOI: https://doi.org/ 10.1016/j.jamda.2014.10.018
28. Prevalence of and interventions for sarcopenia in ageing adults: A systematic review. Report of the International Sarcopenia Initiative (EWGSOP and IWGS) / A. J. Cruz-Jentoft et al. Age Ageing. 2014. Vol. 43, No. 6. P. 48-759.
DOI: https://doi.org/10.1093/ageing/afu115
29. Prevalence of pre-sarcopenia and sarcopenia in Hong Kong chinese geriatric patients with hip fracture and its correlation with different factors / A. W. H. Ho et al. Hong Kong Med. J. 2016. Vol. 22, No. 1. P. 23-29. DOI: https://doi.org/10.12809/hkmj154570
30. Prevalence of sarcopenia in acute hip fracture patients and its influence on short-term clinical
outcome / J. I. Gonzalez-Montalvo et al. Geriatr. Gerontol. Int. 2016. Vol. 16, No. 9. P. 1021-1027. DOI: https://doi.org/10.1111/ggi.12590
31. Prevalence of sarcopenia in the world: A systematic review and meta- analysis of general population studies / G. Shafiee et al. J. Diabetes Metab. Disord. 2017. Vol. 16, No. 1. P. 1-10. DOI: https://doi.org/10.1016/jjamda.2019.09.005
32. Rosenberg I. H. Sarcopenia: Diagnosis and Mechanisms Sarcopenia: Origins and Clinical Relevance 1: Symposium. J. Nutr. 1997. Vol. 127. P. 990-991.
33. Sarcopenia and its association with falls and fractures in older adults: A systematic review and meta-analysis / S. S. Y. Yeung et al. J. Cachexia. Sarcopenia Muscle. 2019. Vol. 10, No. 3. P. 485-500. DOI: https://doi.org/10.1002/jcsm.12411
34. Sarcopenia as a risk factor for falls in elderly individuals: Results from the ilSIRENTE study / F. Landi et al. Clin. Nutr. 2012. Vol. 31, No. 5. P. 652-658. DOI: https://doi.org/10.1016/j.clnu.2012.02.007
35. Sarcopenia: Current treatments and new regenerative therapeutic approaches / Lo J. H. et al. J. Orthop. Transl. 2020. Vol. 23, P. 38-52. DOI: https://doi.org/10.1016/jjot.2020.04.002
36. Sarcopenia: Revised European consensus on definition and diagnosis / A. J. Cruz-Jentoft et al. Age and Ageing. Oxford University Press. 2019. Vol. 48, No. 1. P. 16-31. DOI: https://doi.org/10.1093/ageing/afy169
37. Schaap L. A., Van Schoor N. M., Lips P., Visser M. Associations of sarcopenia definitions, and their components, with the incidence of recurrent falling and fractures: The longitudinal aging study Amsterdam. Journals Gerontol. Ser. A Biol. Sci. Med. Sci. 2018. Vol. 73, No. 9. P. 1199-1204.
DOI: https://doi.org/10.1093/gerona/glx245
38. Sex differences in the prevalence and adverse outcomes of sarcopenia and sarcopenic obesity in community dwelling elderly in East China using the AWGS criteria / Y. Du et al. BMC Endocr Disord. 2019. Vol. 19, No. 109. 11 p.
DOI: https://doi.org/10.1186/s12902-019-0432-x
39. The Future Prevalence of Sarcopenia in Europe: A Claim for Public Health Action / O. Ethgen et al. Calcif. Tissue Int. 2017. Vol. 100, No. 3. P. 229-234. DOI: https://doi.org/doi: 10.1007/s00223-016-0220-9
40. The high prevalence of sarcopenia and its associated outcomes following hip surgery in Taiwanese geriatric patients with a hip fracture/ Y.P. Chen et al. J. Formos. Med. Assoc. 2020. 24 Feb. S0929-6646(20)30041-3. DOI: https://doi.org/10.1016/jjfma.2020.02.004
41. The Impact of Different Diagnostic Criteria on the Prevalence of Sarcopenia in Healthy Elderly Participants and Geriatric Outpatients / E. M. Reijnierse et al., Gerontology. 2015. Vol. 61, No. 6. P. 491-496. DOI: https://doi.org/doi:10.1159/000377699
42. The Joint Occurrence of Osteoporosis and Sarco-penia (Osteosarcopenia): Definitions and Characteristics / W. Sepulveda-Loyola6 et al. J. Am. Med. Dir. Assoc. 2020. Vol. 21, No. 2. P. 220-225.
DOI: https://doi.org/10.1016/jjamda.2019.09.005
43. The relationship between sarcopenia and fragility fracture - a systematic review / R.M.Y. Wong et al. Osteoporos. Int. 2019. Vol. 30, No. 3. P. 541-553. DOI: https://doi.org/10.1007/s00198-018-04828-0
44. Wilson D., Jackson T., Sapey E., Lord J. M. Frailty and sarcopenia: The potential role of an aged immune system. Ageing Res. Rev. 2017. Vol. 36. P. 1-10. DOI: https://doi.org/10.1016Zj.arr.2017.01.006
45. Yu R., Leung J., Woo J. Incremental predictive value of sarcopenia for incident fracture in an elderly chinese cohort: Results from the osteoporotic fractures in men (MrOs) study. J. Am. Med. Dir. Assoc. 2014. Vol. 15, No. 8. P. 551-558. DOI: https://doi.org/10.10167j.jamda.2014.02.005
Стаття надшшла до редакцп 07.09.2020
♦
UDC 616.12-008.331.1:612.614.062-008.6]-073 https://doi.org/10.26641/2307-0404.202L2.234638
algorithm of diagnostics of erectile dysfunction in patients with arterial hypertension and dynamics of arterial blood pressure against the background of androgenic deficiency
Ivano-Frankivsk National Medical University Department of Internal Medicine N1 Halytska str., 2, Ivano-Frankivsk, 76000, Ukraine e-mail: nvchernjuk@gmail.com
Regional Clinical Hospital Municipal Non-Commercial Enterprise of Ivano-Frankivsk Regional Council Fedkovycha str., 91, Ivano-Frankivsk, 76000, Ukraine e-mail: hospital.if.ua@gmail.com
¡вано-Франтський нацюнальний медичний yHieepcumem
кафедра внyтрiшньoi медицини № 1
(зав. - д. мед. н., проф. Н.В. Чернюк)
вул. Галицька, 2,1вано-Франювськ, 76000, Украша
КНП Обласна клiнiчна лiкарня (ОКЛ) 1вано-ФранювсьKoi обласно'1'ради
(головн. лжар - к. мед. н. О.1. Грищук)
вул. Федьковича, 91,1вано-Франювськ, 76000, Украша
Цитування: Медичш перспективы. 2021. Т. 26, № 2. С. 119-125 Cited: Medicni perspektivi. 2021;26(2):119-125
Key words: erectile dysfunction, color Doppler imaging, androgen deficiency, arterial hypertension Ключовi слова: еректильна дисфункщя, кольорова доплерографiя, андрогенний дефщит, apmepicmbna гiпертензiя
Ключевые слова: эректильная дисфункция, цветная допплерография, андрогенный дефицит, артериальная гипертензия
Abstract. Algorithm of diagnostics of erectile dysfunction in patients with arterial hypertension and dynamics of arterial blood pressure against the background of androgenic deficiency. Vintoniv O.R., Popadynets I.R., Hrodzinskyy V.I., Melnyk S.V., Herych P.R., Halipchak I.M. In recent years, the requirements for the level of the
0.R. Vintoniv ,
1.R. Popadynets, V.I. Hrodzinskyy , S.V. Melnyk *, P.R. Herych, I.M. Halipchak *
21/ Том XXVI/ 2
119
