Sarcopenia and Pleural Mesothelioma: The Current Knowledge
Abstract
:1. Introduction
2. Materials and Methods
3. Results
4. Discussion
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- Dacic, S. Pleural mesothelioma classification-update and challenges. Mod. Pathol. 2022, 35, 51–56. [Google Scholar] [CrossRef]
- Beasley, M.B.; Galateau-Salle, F.; Dacic, S. Pleural mesothelioma classification update. Virchows Arch. 2021, 478, 59–72. [Google Scholar] [CrossRef] [PubMed]
- Bibby, A.C.; Tsim, S.; Kanellakis, N.; Ball, H.; Talbot, D.C.; Blyth, K.G.; Maskell, N.A.; Psallidas, I. Malignant pleural mesothelioma: An update on investigation, diagnosis and treatment. Eur. Respir. Rev. 2016, 25, 472–486. [Google Scholar] [CrossRef] [PubMed]
- Mastromarino, M.G.; Lenzini, A.; Aprile, V.; Ali, G.; Bacchin, D.; Korasidis, S.; Ambrogi, M.C.; Lucchi, M. New Insights in Pleural Mesothelioma Classification Update: Diagnostic Traps and Prognostic Implications. Diagnostics 2022, 12, 2905. [Google Scholar] [CrossRef] [PubMed]
- Hung, Y.P.; Chirieac, L.R. Pathology of Malignant Pleural Mesothelioma. Thorac. Surg. Clin. 2020, 30, 367–382. [Google Scholar] [CrossRef] [PubMed]
- Berzenji, L.; Van Schil, P. Multimodality treatment of malignant pleural mesothelioma. F1000Research 2018, 7, 1681. [Google Scholar] [CrossRef]
- Dhillon, R.J.; Hasni, S. Pathogenesis and Management of Sarcopenia. Clin. Geriatr. Med. 2017, 33, 17–26. [Google Scholar] [CrossRef]
- Dodds, R.M.; Roberts, H.C.; Cooper, C.; Sayer, A.A. The Epidemiology of Sarcopenia. J. Clin. Densitom. 2015, 18, 461–466. [Google Scholar] [CrossRef]
- Karakousis, N.D.; Pyrgioti, E.E.; Georgakopoulos, P.N.; Papanas, N. Sarcopenia, Frailty and Diabetic Foot: A Mini Narrative Review. Int. J. Low. Extrem. Wounds 2022. [Google Scholar] [CrossRef]
- Sayer, A.A.; Cruz-Jentoft, A. Sarcopenia definition, diagnosis and treatment: Consensus is growing. Age Ageing 2022, 51, afac220. [Google Scholar] [CrossRef]
- Coletta, G.; Phillips, S.M. An elusive consensus definition of sarcopenia impedes research and clinical treatment: A narrative review. Ageing Res. Rev. 2023, 86, 101883. [Google Scholar] [CrossRef]
- Karakousis, N.D.; Gourgoulianis, K.I.; Kotsiou, O.S. Sarcopenia and Tuberculosis: Is There Any Connection? J. Pers. Med. 2023, 13, 1102. [Google Scholar] [CrossRef]
- Xia, L.; Zhao, R.; Wan, Q.; Wu, Y.; Zhou, Y.; Wang, Y.; Cui, Y.; Shen, X.; Wu, X. Sarcopenia and adverse health-related outcomes: An umbrella review of meta-analyses of observational studies. Cancer Med. 2020, 9, 7964–7978. [Google Scholar] [CrossRef]
- Cho, M.R.; Lee, S.; Song, S.K. A Review of Sarcopenia Pathophysiology, Diagnosis, Treatment and Future Direction. J. Korean Med. Sci. 2022, 37, e146. [Google Scholar] [CrossRef]
- Pyrgioti, E.E.; Karakousis, N.D.; Georgakopoulos, P.N.; Papanas, N. Metformin in type 2 diabetes: Evidence for its beneficial effects on frailty and sarcopenia. Curr. Diabetes Rev. 2023, 20, e270723219177. [Google Scholar] [CrossRef]
- Karakousis, N.D.; Chrysavgis, L.; Chatzigeorgiou, A.; Papatheodoridis, G.; Cholongitas, E. Frailty in metabolic syndrome, focusing on nonalcoholic fatty liver disease. Ann. Gastroenterol. 2022, 35, 234–242. [Google Scholar] [CrossRef] [PubMed]
- Karakousis, N.D.; Kostakopoulos, N.A. Hyponatremia in the frail. J. Frailty Sarcopenia Falls 2021, 6, 241–245. [Google Scholar] [CrossRef] [PubMed]
- Bellos, T.C.; Tzelves, L.I.; Manolitsis, I.S.; Katsimperis, S.N.; Berdempes, M.V.; Skolarikos, A.; Karakousis, N.D. Frailty and benign prostatic hyperplasia: The thrilling underlying impact. Arch. Ital. Urol. Androl. 2022, 94, 345–349. [Google Scholar] [CrossRef]
- Nascimento, C.M.; Ingles, M.; Salvador-Pascual, A.; Cominetti, M.R.; Gomez-Cabrera, M.C.; Vina, J. Sarcopenia, frailty and their prevention by exercise. Free Radic. Biol. Med. 2019, 132, 42–49. [Google Scholar] [CrossRef] [PubMed]
- Martin, F.C.; O’Halloran, A.M. Tools for Assessing Frailty in Older People: General Concepts. Adv. Exp. Med. Biol. 2020, 1216, 9–19. [Google Scholar] [CrossRef] [PubMed]
- Ferrer, M.; Anthony, T.G.; Ayres, J.S.; Biffi, G.; Brown, J.C.; Caan, B.J.; Cespedes Feliciano, E.M.; Coll, A.P.; Dunne, R.F.; Goncalves, M.D.; et al. Cachexia: A systemic consequence of progressive, unresolved disease. Cell 2023, 186, 1824–1845. [Google Scholar] [CrossRef]
- Cruz-Jentoft, A.J.; Bahat, G.; Bauer, J.; Boirie, Y.; Bruyere, O.; Cederholm, T.; Cooper, C.; Landi, F.; Rolland, Y.; Sayer, A.A.; et al. Sarcopenia: Revised European consensus on definition and diagnosis. Age Ageing 2019, 48, 16–31. [Google Scholar] [CrossRef]
- Bahat, G.; Erdogan, T.; Ilhan, B. SARC-F and other screening tests for sarcopenia. Curr. Opin. Clin. Nutr. Metab. Care 2022, 25, 37–42. [Google Scholar] [CrossRef] [PubMed]
- Duarte, M.P.; Ribeiro, H.S.; Almeida, L.S.; Baiao, V.M.; Inda-Filho, A.; Avesani, C.M.; Ferreira, A.P.; Lima, R.M. SARC-F and SARC-CalF are associated with sarcopenia traits in hemodialysis patients. Nutr. Clin. Pract. 2022, 37, 1356–1365. [Google Scholar] [CrossRef]
- Ida, S.; Kaneko, R.; Murata, K. SARC-F for Screening of Sarcopenia Among Older Adults: A Meta-analysis of Screening Test Accuracy. J. Am. Med. Dir. Assoc. 2018, 19, 685–689. [Google Scholar] [CrossRef] [PubMed]
- Thompson, M.Q.; Jadczak, A.D.; Yu, S.; Tucker, G.R.; Visvanathan, R. Sarcopenia risk in nursing home residents using SARC-F: FIRST study findings. Geriatr. Gerontol. Int. 2022, 22, 206–212. [Google Scholar] [CrossRef]
- Do, J.Y.; Seo, J.H.; Kang, S.H. Validation of the SARC-F for Assessing Sarcopenia in Patients on Peritoneal Dialysis. J. Ren. Nutr. 2022, 32, 341–346. [Google Scholar] [CrossRef]
- Nishikawa, H.; Asai, A.; Fukunishi, S.; Takeuchi, T.; Goto, M.; Ogura, T.; Nakamura, S.; Kakimoto, K.; Miyazaki, T.; Nishiguchi, S.; et al. Screening Tools for Sarcopenia. In Vivo 2021, 35, 3001–3009. [Google Scholar] [CrossRef] [PubMed]
- Peng, T.C.; Chiou, J.M.; Chen, T.F.; Chen, Y.C.; Chen, J.H. Grip Strength and Sarcopenia Predict 2-Year Cognitive Impairment in Community-Dwelling Older Adults. J. Am. Med. Dir. Assoc. 2023, 24, 292–298.e1. [Google Scholar] [CrossRef]
- Zhao, H.; Cheng, R.; Song, G.; Teng, J.; Shen, S.; Fu, X.; Yan, Y.; Liu, C. The Effect of Resistance Training on the Rehabilitation of Elderly Patients with Sarcopenia: A Meta-Analysis. Int. J. Environ. Res. Public Health 2022, 19, 15491. [Google Scholar] [CrossRef]
- He, H.; Pan, L.; Wang, D.; Liu, F.; Du, J.; Pa, L.; Wang, X.; Cui, Z.; Ren, X.; Wang, H.; et al. Normative values of hand grip strength in a large unselected Chinese population: Evidence from the China National Health Survey. J. Cachexia Sarcopenia Muscle 2023, 14, 1312–1321. [Google Scholar] [CrossRef]
- Chou, M.Y.; Nishita, Y.; Nakagawa, T.; Tange, C.; Tomida, M.; Shimokata, H.; Otsuka, R.; Chen, L.K.; Arai, H. Role of gait speed and grip strength in predicting 10-year cognitive decline among community-dwelling older people. BMC Geriatr. 2019, 19, 186. [Google Scholar] [CrossRef]
- Dodds, R.M.; Syddall, H.E.; Cooper, R.; Benzeval, M.; Deary, I.J.; Dennison, E.M.; Der, G.; Gale, C.R.; Inskip, H.M.; Jagger, C.; et al. Grip strength across the life course: Normative data from twelve British studies. PLoS ONE 2014, 9, e113637. [Google Scholar] [CrossRef]
- De, A.; Kumari, S.; Kaur, A.; Singh, A.; Kalra, N.; Singh, V. Hand-grip strength as a screening tool for sarcopenia in males with decompensated cirrhosis. Indian. J. Gastroenterol. 2022, 41, 284–291. [Google Scholar] [CrossRef]
- Roberts, H.C.; Denison, H.J.; Martin, H.J.; Patel, H.P.; Syddall, H.; Cooper, C.; Sayer, A.A. A review of the measurement of grip strength in clinical and epidemiological studies: Towards a standardised approach. Age Ageing 2011, 40, 423–429. [Google Scholar] [CrossRef] [PubMed]
- Albano, D.; Messina, C.; Vitale, J.; Sconfienza, L.M. Imaging of sarcopenia: Old evidence and new insights. Eur. Radiol. 2020, 30, 2199–2208. [Google Scholar] [CrossRef]
- Zwart, A.T.; Becker, J.N.; Lamers, M.J.; Dierckx, R.; de Bock, G.H.; Halmos, G.B.; van der Hoorn, A. Skeletal muscle mass and sarcopenia can be determined with 1.5-T and 3-T neck MRI scans, in the event that no neck CT scan is performed. Eur. Radiol. 2021, 31, 4053–4062. [Google Scholar] [CrossRef] [PubMed]
- Vogele, D.; Otto, S.; Sollmann, N.; Haggenmuller, B.; Wolf, D.; Beer, M.; Schmidt, S.A. Sarcopenia—Definition, Radiological Diagnosis, Clinical Significance. Rofo 2023, 195, 393–405. [Google Scholar] [CrossRef]
- Beer, L.; Bastati, N.; Ba-Ssalamah, A.; Potter-Lang, S.; Lampichler, K.; Bican, Y.; Lauber, D.; Hodge, J.; Binter, T.; Pomej, K.; et al. MRI-defined sarcopenia predicts mortality in patients with chronic liver disease. Liver Int. 2020, 40, 2797–2807. [Google Scholar] [CrossRef] [PubMed]
- Jimenez-Gutierrez, G.E.; Martinez-Gomez, L.E.; Martinez-Armenta, C.; Pineda, C.; Martinez-Nava, G.A.; Lopez-Reyes, A. Molecular Mechanisms of Inflammation in Sarcopenia: Diagnosis and Therapeutic Update. Cells 2022, 11, 2359. [Google Scholar] [CrossRef]
- Cheng, K.Y.; Chow, S.K.; Hung, V.W.; Wong, C.H.; Wong, R.M.; Tsang, C.S.; Kwok, T.; Cheung, W.H. Diagnosis of sarcopenia by evaluating skeletal muscle mass by adjusted bioimpedance analysis validated with dual-energy X-ray absorptiometry. J. Cachexia Sarcopenia Muscle 2021, 12, 2163–2173. [Google Scholar] [CrossRef]
- Ticinesi, A.; Meschi, T.; Narici, M.V.; Lauretani, F.; Maggio, M. Muscle Ultrasound and Sarcopenia in Older Individuals: A Clinical Perspective. J. Am. Med. Dir. Assoc. 2017, 18, 290–300. [Google Scholar] [CrossRef]
- Guglielmi, G.; Ponti, F.; Agostini, M.; Amadori, M.; Battista, G.; Bazzocchi, A. The role of DXA in sarcopenia. Aging Clin. Exp. Res. 2016, 28, 1047–1060. [Google Scholar] [CrossRef]
- Tagliafico, A.S.; Bignotti, B.; Torri, L.; Rossi, F. Sarcopenia: How to measure, when and why. Radiol. Med. 2022, 127, 228–237. [Google Scholar] [CrossRef] [PubMed]
- Di Vincenzo, O.; Marra, M.; Di Gregorio, A.; Pasanisi, F.; Scalfi, L. Bioelectrical impedance analysis (BIA) -derived phase angle in sarcopenia: A systematic review. Clin. Nutr. 2021, 40, 3052–3061. [Google Scholar] [CrossRef] [PubMed]
- Bise, T.; Yoshimura, Y.; Wakabayashi, H.; Nagano, F.; Kido, Y.; Shimazu, S.; Shiraishi, A.; Matsumoto, A. Association between BIA-derived Phase Angle and Sarcopenia and Improvement in Activities of Daily Living and Dysphagia in Patients undergoing Post-Stroke Rehabilitation. J. Nutr. Health Aging 2022, 26, 590–597. [Google Scholar] [CrossRef] [PubMed]
- Akamatsu, Y.; Kusakabe, T.; Arai, H.; Yamamoto, Y.; Nakao, K.; Ikeue, K.; Ishihara, Y.; Tagami, T.; Yasoda, A.; Ishii, K.; et al. Phase angle from bioelectrical impedance analysis is a useful indicator of muscle quality. J. Cachexia Sarcopenia Muscle 2022, 13, 180–189. [Google Scholar] [CrossRef] [PubMed]
- Antoniak, A.E.; Greig, C.A. The effect of combined resistance exercise training and vitamin D(3) supplementation on musculoskeletal health and function in older adults: A systematic review and meta-analysis. BMJ Open 2017, 7, e014619. [Google Scholar] [CrossRef] [PubMed]
- Kostka, J.; Sosowska, N.; Guligowska, A.; Kostka, T. A Proposed Method of Converting Gait Speed and TUG Test in Older Subjects. Int. J. Environ. Res. Public Health 2022, 19, 12145. [Google Scholar] [CrossRef] [PubMed]
- Marcos-Pardo, P.J.; Gonzalez-Galvez, N.; Carbonell-Baeza, A.; Jimenez-Pavon, D.; Vaquero-Cristobal, R. GDLAM and SPPB batteries for screening sarcopenia in community-dwelling Spanish older adults: Healthy-age network study. Exp. Gerontol. 2023, 172, 112044. [Google Scholar] [CrossRef] [PubMed]
- Perez-Sousa, M.A.; Venegas-Sanabria, L.C.; Chavarro-Carvajal, D.A.; Cano-Gutierrez, C.A.; Izquierdo, M.; Correa-Bautista, J.E.; Ramirez-Velez, R. Gait speed as a mediator of the effect of sarcopenia on dependency in activities of daily living. J. Cachexia Sarcopenia Muscle 2019, 10, 1009–1015. [Google Scholar] [CrossRef] [PubMed]
- Wu, X.; Li, X.; Xu, M.; Zhang, Z.; He, L.; Li, Y. Sarcopenia prevalence and associated factors among older Chinese population: Findings from the China Health and Retirement Longitudinal Study. PLoS ONE 2021, 16, e0247617. [Google Scholar] [CrossRef] [PubMed]
- Merchant, R.A.; Chan, Y.H.; Hui, R.J.Y.; Lim, J.Y.; Kwek, S.C.; Seetharaman, S.K.; Au, L.S.Y.; Morley, J.E. Possible Sarcopenia and Impact of Dual-Task Exercise on Gait Speed, Handgrip Strength, Falls, and Perceived Health. Front. Med. 2021, 8, 660463. [Google Scholar] [CrossRef] [PubMed]
- Hurst, C.; Robinson, S.M.; Witham, M.D.; Dodds, R.M.; Granic, A.; Buckland, C.; De Biase, S.; Finnegan, S.; Rochester, L.; Skelton, D.A.; et al. Resistance exercise as a treatment for sarcopenia: Prescription and delivery. Age Ageing 2022, 51, afac003. [Google Scholar] [CrossRef]
- Shen, Y.; Shi, Q.; Nong, K.; Li, S.; Yue, J.; Huang, J.; Dong, B.; Beauchamp, M.; Hao, Q. Exercise for sarcopenia in older people: A systematic review and network meta-analysis. J. Cachexia Sarcopenia Muscle 2023, 14, 1199–1211. [Google Scholar] [CrossRef]
- Landi, F.; Marzetti, E.; Martone, A.M.; Bernabei, R.; Onder, G. Exercise as a remedy for sarcopenia. Curr. Opin. Clin. Nutr. Metab. Care 2014, 17, 25–31. [Google Scholar] [CrossRef]
- Phu, S.; Boersma, D.; Duque, G. Exercise and Sarcopenia. J. Clin. Densitom. 2015, 18, 488–492. [Google Scholar] [CrossRef]
- Bauer, J.; Biolo, G.; Cederholm, T.; Cesari, M.; Cruz-Jentoft, A.J.; Morley, J.E.; Phillips, S.; Sieber, C.; Stehle, P.; Teta, D.; et al. Evidence-based recommendations for optimal dietary protein intake in older people: A position paper from the PROT-AGE Study Group. J. Am. Med. Dir. Assoc. 2013, 14, 542–559. [Google Scholar] [CrossRef]
- Ganapathy, A.; Nieves, J.W. Nutrition and Sarcopenia-What Do We Know? Nutrients 2020, 12, 1755. [Google Scholar] [CrossRef]
- Detopoulou, P.; Voulgaridou, G.; Papadopoulou, S. Cancer, Phase Angle and Sarcopenia: The Role of Diet in Connection with Lung Cancer Prognosis. Lung 2022, 200, 347–379. [Google Scholar] [CrossRef]
- Peterson, S.J.; Mozer, M. Differentiating Sarcopenia and Cachexia Among Patients With Cancer. Nutr. Clin. Pract. 2017, 32, 30–39. [Google Scholar] [CrossRef]
- Jeffery, E.; Lee, Y.C.G.; Newton, R.U.; Lyons-Wall, P.; McVeigh, J.; Nowak, A.K.; Cheah, H.M.; Nguyen, B.; Fitzgerald, D.B.; Creaney, J.; et al. Body composition and nutritional status in malignant pleural mesothelioma: Implications for activity levels and quality of life. Eur. J. Clin. Nutr. 2019, 73, 1412–1421. [Google Scholar] [CrossRef]
- Jeffery, E.; Lee, Y.C.G.; Newton, R.U.; Lyons-Wall, P.; McVeigh, J.; Fitzgerald, D.B.; Straker, L.; Peddle-McIntyre, C.J. Changes in body composition in patients with malignant pleural mesothelioma and the relationship with activity levels and dietary intake. Eur. J. Clin. Nutr. 2022, 76, 979–986. [Google Scholar] [CrossRef]
- Verhoek, O.G.; Jungblut, L.; Lauk, O.; Bluthgen, C.; Opitz, I.; Frauenfelder, T.; Martini, K. Sarcopenia, Precardial Adipose Tissue and High Tumor Volume as Outcome Predictors in Surgically Treated Pleural Mesothelioma. Diagnostics 2022, 12, 99. [Google Scholar] [CrossRef]
- Faccioli, E.; Terzi, S.; Giraudo, C.; Zuin, A.; Modugno, A.; Labella, F.; Zambello, G.; Lorenzoni, G.; Schiavon, M.; Gregori, D.; et al. Sarcopenia as a Predictor of Short- and Long-Term Outcomes in Patients Surgically Treated for Malignant Pleural Mesothelioma. Cancers 2022, 14, 3699. [Google Scholar] [CrossRef] [PubMed]
- Williams, G.R.; Dunne, R.F.; Giri, S.; Shachar, S.S.; Caan, B.J. Sarcopenia in the Older Adult With Cancer. J. Clin. Oncol. 2021, 39, 2068–2078. [Google Scholar] [CrossRef] [PubMed]
- Sun, Q.; Jiang, X.; Qin, R.; Yang, Y.; Gong, Y.; Wang, K.; Peng, J. Sarcopenia among older patients with cancer: A scoping review of the literature. J. Geriatr. Oncol. 2022, 13, 924–934. [Google Scholar] [CrossRef] [PubMed]
- Chindapasirt, J. Sarcopenia in Cancer Patients. Asian Pac. J. Cancer Prev. 2015, 16, 8075–8077. [Google Scholar] [CrossRef] [PubMed]
- Meza-Valderrama, D.; Marco, E.; Davalos-Yerovi, V.; Muns, M.D.; Tejero-Sanchez, M.; Duarte, E.; Sanchez-Rodriguez, D. Sarcopenia, Malnutrition, and Cachexia: Adapting Definitions and Terminology of Nutritional Disorders in Older People with Cancer. Nutrients 2021, 13, 761. [Google Scholar] [CrossRef] [PubMed]
- Jogiat, U.; Jimoh, Z.; Turner, S.R.; Baracos, V.; Eurich, D.; Bedard, E.L.R. Sarcopenia in Lung Cancer: A Narrative Review. Nutr. Cancer 2023, 75, 1485–1498. [Google Scholar] [CrossRef]
- Morton, M.; Patterson, J.; Sciuva, J.; Perni, J.; Backes, F.; Nagel, C.; O’Malley, D.M.; Chambers, L.M. Malnutrition, sarcopenia, and cancer cachexia in gynecologic cancer. Gynecol. Oncol. 2023, 175, 142–155. [Google Scholar] [CrossRef]
- Jovanovic, N.; Chinnery, T.; Mattonen, S.A.; Palma, D.A.; Doyle, P.C.; Theurer, J.A. Sarcopenia in head and neck cancer: A scoping review. PLoS ONE 2022, 17, e0278135. [Google Scholar] [CrossRef]
- Zhang, F.M.; Song, C.H.; Guo, Z.Q.; Yu, Z.; Weng, M.; Zhou, F.X.; Liu, M.; Cong, M.H.; Li, T.; Li, Z.N.; et al. Sarcopenia prevalence in patients with cancer and association with adverse prognosis: A nationwide survey on common cancers. Nutrition 2023, 114, 112107. [Google Scholar] [CrossRef]
- Fukushima, H.; Takemura, K.; Suzuki, H.; Koga, F. Impact of Sarcopenia as a Prognostic Biomarker of Bladder Cancer. Int. J. Mol. Sci. 2018, 19, 2999. [Google Scholar] [CrossRef]
- Ongaro, E.; Buoro, V.; Cinausero, M.; Caccialanza, R.; Turri, A.; Fanotto, V.; Basile, D.; Vitale, M.G.; Ermacora, P.; Cardellino, G.G.; et al. Sarcopenia in gastric cancer: When the loss costs too much. Gastric Cancer 2017, 20, 563–572. [Google Scholar] [CrossRef]
- Zhang, F.M.; Wu, H.F.; Shi, H.P.; Yu, Z.; Zhuang, C.L. Sarcopenia and malignancies: Epidemiology, clinical classification and implications. Ageing Res. Rev. 2023, 91, 102057. [Google Scholar] [CrossRef]
- Basile, D.; Corvaja, C.; Caccialanza, R.; Aprile, G. Sarcopenia: Looking to muscle mass to better manage pancreatic cancer patients. Curr. Opin. Support. Palliat. Care 2019, 13, 279–285. [Google Scholar] [CrossRef]
- Fukushima, H.; Koga, F. Impact of sarcopenia in the management of urological cancer patients. Expert. Rev. Anticancer Ther. 2017, 17, 455–466. [Google Scholar] [CrossRef] [PubMed]
- Yamada, R.; Todo, Y.; Minowa, K.; Minobe, S.; Suzuki, Y.; Kato, H.; Kurosu, H.; Mori, Y.; Osanai, T. Prevalence of sarcopenia in patients with gynecological cancer. Jpn. J. Clin. Oncol. 2022, 52, 1001–1007. [Google Scholar] [CrossRef] [PubMed]
- Watanabe, A.; Oshikiri, T.; Sawada, R.; Harada, H.; Urakawa, N.; Goto, H.; Hasegawa, H.; Kanaji, S.; Yamashita, K.; Matsuda, T.; et al. Actual Sarcopenia Reflects Poor Prognosis in Patients with Esophageal Cancer. Ann. Surg. Oncol. 2022, 29, 3670–3681. [Google Scholar] [CrossRef] [PubMed]
- Rossi, F.; Lambertini, M.; Brunetti, N.; De Giorgis, S.; Razeti, M.G.; Calabrese, M.; Tagliafico, A.S. Muscle mass loss in breast cancer patients of reproductive age (</= 45 years) undergoing neoadjuvant chemotherapy. Radiol. Med. 2023, 128, 49–57. [Google Scholar] [CrossRef] [PubMed]
- Bland, K.A.; Kouw, I.W.K.; van Loon, L.J.C.; Zopf, E.M.; Fairman, C.M. Exercise-Based Interventions to Counteract Skeletal Muscle Mass Loss in People with Cancer: Can We Overcome the Odds? Sports Med. 2022, 52, 1009–1027. [Google Scholar] [CrossRef] [PubMed]
- Solomayer, E.F.; Braun, E.M.; Zimmermann, J.S.M.; Radosa, J.C.; Stroeder, J.; Endrikat, J.; Gerlinger, C. Muscle mass loss in patients with metastatic breast cancer. Arch. Gynecol. Obstet. 2019, 300, 201–206. [Google Scholar] [CrossRef] [PubMed]
- Ryan, A.M.; Prado, C.M.; Sullivan, E.S.; Power, D.G.; Daly, L.E. Effects of weight loss and sarcopenia on response to chemotherapy, quality of life, and survival. Nutrition 2019, 67–68, 110539. [Google Scholar] [CrossRef]
- Davis, M.P.; Panikkar, R. Sarcopenia associated with chemotherapy and targeted agents for cancer therapy. Ann. Palliat. Med. 2019, 8, 86–101. [Google Scholar] [CrossRef] [PubMed]
- Imamura, K.; Yamamoto, S.; Suzuki, Y.; Matsuzawa, R.; Harada, M.; Yoshikoshi, S.; Yoshida, A.; Matsunaga, A. Limitations of SARC-F as a Screening Tool for Sarcopenia in Patients on Hemodialysis. Nephron 2022, 146, 32–39. [Google Scholar] [CrossRef]
- Ha, Y.C.; Hwang, S.C.; Song, S.Y.; Lee, C.; Park, K.S.; Yoo, J.I. Hand grip strength measurement in different epidemiologic studies using various methods for diagnosis of sarcopenia: A systematic review. Eur. Geriatr. Med. 2018, 9, 277–288. [Google Scholar] [CrossRef] [PubMed]
- Barreto de Lima, A.; Dos Santos Ribeiro, G.; Henriques-Neto, D.; Rubio Gouveia, E.; Baptista, F. Diagnostic performance of SARC-F and SARC-CalF in screening for sarcopenia in older adults in Northern Brazil. Sci. Rep. 2023, 13, 11698. [Google Scholar] [CrossRef]
- Lu, J.L.; Ding, L.Y.; Xu, Q.; Zhu, S.Q.; Xu, X.Y.; Hua, H.X.; Chen, L.; Xu, H. Screening Accuracy of SARC-F for Sarcopenia in the Elderly: A Diagnostic Meta-Analysis. J. Nutr. Health Aging 2021, 25, 172–182. [Google Scholar] [CrossRef]
- Hess, D.L.; Harmon, C.; Bhatia, S.; Williams, G.R.; Giri, S. SARC-F as a screening tool to detect computed tomography-based sarcopenia and myosteatosis among older adults with cancer. Cancer Med. 2023, 12, 20690–20698. [Google Scholar] [CrossRef]
- Sato, T.; Aoyama, T.; Hayashi, T.; Segami, K.; Kawabe, T.; Fujikawa, H.; Yamada, T.; Yamamoto, N.; Oshima, T.; Rino, Y.; et al. Impact of preoperative hand grip strength on morbidity following gastric cancer surgery. Gastric Cancer 2016, 19, 1008–1015. [Google Scholar] [CrossRef]
- Kim, S.; Yoon, H.K.; Rhee, C.K.; Jung, H.W.; Lee, H.; Jo, Y.S. Hand Grip Strength and Likelihood of Moderate-to-Severe Airflow Limitation in the General Population. Int. J. Chronic Obstr. Pulm. Dis. 2022, 17, 1237–1245. [Google Scholar] [CrossRef]
- Lim, J.P.; Yew, S.; Tay, L.; Chew, J.; Yeo, A.; Hafizah Ismail, N.; Ding, Y.Y.; Lim, W.S. Grip Strength Criterion Matters: Impact of Average Versus Maximum Handgrip Strength on Sarcopenia Prevalence and Predictive Validity for Low Physical Performance. J. Nutr. Health Aging 2020, 24, 1031–1035. [Google Scholar] [CrossRef]
Authors/[Ref] | Study Type | Study Population | Main Results | Sarcopenia Evaluation |
---|---|---|---|---|
Jeffery et al. [62] | Cross-sectional analysis | 61 MPM subjects, 79% male with median age 69 (62–74) years | 54% were pre-sarcopenic and 38% were malnourished. The light activity period percent per day was lower in subjects with pre-sarcopenia in comparison with non-sarcopenic subjects (p = 0.008). Subjects with malnutrition had worse HRQoL than well-nourished subjects (p < 0.001). | ASM measured via DXA |
Jeffery et al. [63] | Observational study | 18 MPM subjects (89% men, mean age 68.9 ± 7.1 years) | In comparison with subjects with ASM maintenance (n = 9), fewer subjects with ASM loss (n = 9) survived ≥12 months from follow-up (p = 0.002). Subjects with ASM loss had augmented sedentary time (p = 0.028) and lowered light activity (p = 0.028) and step count (p = 0.008). Activity levels did not alter in subjects with ASM maintenance (p > 0.05), while both energy and protein intake did not demonstrate any alteration in either group (p > 0.05). | DXA |
Verhoek et al. [64] | Retrospective study | 278 PM-subjects (252 male, 70.2 ± 9 years) | Mean progression-free survival was 18.6 ± 12.2 months. Mean survival period was 23.3 ± 24 months. Progression related to COPD (p < 0.001), type of surgery (p = 0.026), tumor stage (p = 0.001). Three-year mortality related to higher subject age (p = 0.005), increased tumor stage (p = 0.015), presence of COPD (p < 0.001), increased tumor volume (p < 0.001). Sarcopenic subjects had increased three-year mortality (p = 0.002). Even though there was an inverse correlation of progression-free survival and mortality with tumor volume (r = 0.281, p = 0.001 and r = −0.240, p < 0.001, respectively), a correlation with PAT was only demonstrated for epithelioid PM (p = 0.040) | CT-based parameters evaluated at TH5 level, excluding fatty infiltration based on CT attenuation |
Faccioli et al. [65] | Single-center retrospective study | 86 subjects surgically treated for MPM [mean age: 66 (62–71 years), 76% males] | Sarcopenia pre-operatively present in 57 (66%) subjects and post-operatively in 61 (74%). Post-operative sarcopenic subjects had decreased 3-year OS than non-sarcopenic (p = 0.03). Pre-operative sarcopenia importantly related to increased frequency of post-operative adverse outcomes (p = 0.04) | Mean muscular density of the bilateral paravertebral muscles (T12 level) on pre- and post-operative CTs |
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Karakousis, N.D.; Gourgoulianis, K.I.; Papanas, N.; Kotsiou, O.S. Sarcopenia and Pleural Mesothelioma: The Current Knowledge. Muscles 2024, 3, 48-59. https://doi.org/10.3390/muscles3010006
Karakousis ND, Gourgoulianis KI, Papanas N, Kotsiou OS. Sarcopenia and Pleural Mesothelioma: The Current Knowledge. Muscles. 2024; 3(1):48-59. https://doi.org/10.3390/muscles3010006
Chicago/Turabian StyleKarakousis, Nikolaos D., Konstantinos I. Gourgoulianis, Nikolaos Papanas, and Ourania S. Kotsiou. 2024. "Sarcopenia and Pleural Mesothelioma: The Current Knowledge" Muscles 3, no. 1: 48-59. https://doi.org/10.3390/muscles3010006
APA StyleKarakousis, N. D., Gourgoulianis, K. I., Papanas, N., & Kotsiou, O. S. (2024). Sarcopenia and Pleural Mesothelioma: The Current Knowledge. Muscles, 3(1), 48-59. https://doi.org/10.3390/muscles3010006