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Chronic kidney disease and premature ageing
Jeroen P Kooman1, Peter Kotanko2, Annemie M W J Schols3
1Department of Internal Medicine, Division of Nephrology, Maastricht University Medical Center, PO Box 5800, 6202 AZ Maastrich, Netherlands.
Insights
Chronic kidney disease (CKD) accelerates aging, causing vascular disease and muscle wasting. Understanding these mechanisms can improve treatments for CKD and other chronic conditions.
Area of Science:
- Nephrology
- Gerontology
- Internal Medicine
Background:
- Chronic kidney disease (CKD) exhibits phenotypic similarities to other chronic diseases like heart failure and rheumatoid arthritis.
- Premature aging, characterized by accelerated vascular disease and muscle wasting, is a key shared feature.
Purpose of the Study:
- To explore disease-induced mechanisms driving premature aging in CKD.
- To identify potential interventions for mitigating aging phenotypes in chronic diseases.
Main Methods:
- Review and synthesis of proposed mechanisms of premature aging in CKD.
- Analysis of current interventions targeting premature aging in chronic diseases.
Main Results:
- Four key mechanisms contribute to premature aging in CKD: increased allostatic load, stress response activation, promotion of aging, and impaired anti-aging pathways.
- Effective interventions (disease treatment, nutrition, exercise) reduce inflammation and oxidative stress, promoting muscle growth.
Conclusions:
- Mechanistic insights into premature aging in CKD can enhance intervention efficacy.
- Early CKD diagnosis and targeted therapies may combat muscle wasting and vascular issues in chronic diseases.
Abstract:
Chronic kidney disease (CKD) shares many phenotypic similarities with other chronic diseases, including heart failure, chronic obstructive pulmonary disease, HIV infection and rheumatoid arthritis. The most apparent similarity is premature ageing, involving accelerated vascular disease and muscle wasting. We propose that in addition to a sedentary lifestyle and psychosocial and socioeconomic determinants, four major disease-induced mechanisms underlie premature ageing in CKD: an increase in allostatic load, activation of the 'stress resistance response', activation of age-promoting mechanisms and impairment of anti-ageing pathways. The most effective current interventions to modulate premature ageing-treatment of the underlying disease, optimal nutrition, correction of the internal environment and exercise training-reduce systemic inflammation and oxidative stress and induce muscle anabolism. Deeper mechanistic insight into the phenomena of premature ageing as well as early diagnosis of CKD might improve the application and efficacy of these interventions and provide novel leads to combat muscle wasting and vascular impairment in chronic diseases.
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