Association Between Advanced Glycation End Products and Sarcopenia: The Mediating Role of Osteoporosis

Author:

Zhang Xingyu12ORCID,Chen Xiaoyu1,Li Shengjie12,Gao Mengze12,Han Peipei1,Cao Liou3,Gao Jing4,Tao Qiongying5,Zhai Jiayi5,Liang Dongyu6,Qin Li7,Guo Qi1ORCID

Affiliation:

1. Department of Rehabilitation Medicine, Shanghai University of Medicine and Health Sciences Affiliated Zhoupu Hospital , Shanghai 201318 , China

2. Tianjin Key Laboratory of Exercise Physiology and Sports Medicine, Institute of Sport, Exercise & Health, Tianjin University of Sport , Tianjin 300381 , China

3. Department of Nephrology, Molecular Cell Lab for Kidney Disease, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine , Shanghai 200127 , China

4. General Practice Clinic, Pujiang Community Health Service Center in Minhang District , Shanghai 201112 , China

5. Jiading Subdistrict Community Health Center , Shanghai 201899 , China

6. Clinical Research Center, Jiading District Central Hospital Affiliated Shanghai University of Medicine & Health Sciences , Shanghai 201800 , China

7. Department of General Medicine, Jiading Subdistrict Community Health Center , Shanghai 201899 , China

Abstract

Abstract Context Advanced glycation end products (AGEs) are a group of molecules formed through nonenzymatic reactions. These compounds are associated with several age-related diseases, including sarcopenia and osteoporosis. Objective This work aimed to investigate the relationships between AGEs, osteoporosis, and sarcopenia in community-dwelling older adults. Methods This cross-sectional study included 1991 older adults aged 72.37 ± 5.90 years from China. AGE levels were measured by the AGE Reader device. Bone mineral density was assessed using dual-energy X-ray absorptiometry, and osteoporosis was diagnosed based on a T score of less than −2.5. Sarcopenia was defined as loss of muscle mass plus loss of muscle strength and/or reduced physical performance. Presarcopenia was defined as low muscle mass with normal muscle strength and normal physical performance. Results The prevalence of sarcopenia was 18.5%, and that of osteoporosis was 40.5%. Compared to the lowest AGE quartile, the highest AGE quartile showed a significant association with sarcopenia (odds ratio [OR] 2.42; 95% CI, 1.60-3.66) (P for trend <.001), but not with presarcopenia. Per-SD increase in AGE was associated with higher odds of sarcopenia (OR 1.44; 95% CI, 1.26-1.66). Additionally, in the mediation analysis, when AGEs were treated as a continuous variable (the mediation effect is denoted by Za*Zb = 18.81; 95% CI, 8.07-32.32]—the 95% CI does not contain zero, representing a significant mediating effect) or a categorical variable (the mediating effect is expressed as Zmediation = 3.01 > 1.96, which represents a significant mediating effect), osteoporosis played a partial mediating role in the association between AGEs and sarcopenia. Conclusion Elevated AGEs are associated with sarcopenia but not with presarcopenia. This association was partially mediated by osteoporosis.

Funder

Capacity Building project of Local Colleges of Shanghai Science and Technology Commission

Shanghai Sailing Program

Shanghai Municipal Health Commission

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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