Circulating lipocalin-2 across the adult lifespan.

Carlie Bauer, Cassandra Smith, Sara Vogrin, Andrew S Palmer, Mary Woessner, Shanie Landen, Macsue Jacques, Elizabeth Byrnes, Nir Eynon, Marc Sim, Joshua R Lewis, Itamar Levinger
Author Information
  1. Carlie Bauer: Institute for Health and Sport, Victoria University, Melbourne, VIC 3011, Australia.
  2. Cassandra Smith: Nutrition & Health Innovation Research Institute, Edith Cowan University, Joondalup, WA 6027, Australia. ORCID
  3. Sara Vogrin: Australian Institute for Musculoskeletal Science, Victoria University, University of Melbourne, St Albans, VIC 3021, Australia.
  4. Andrew S Palmer: Institute for Health and Sport, Victoria University, Melbourne, VIC 3011, Australia.
  5. Mary Woessner: Institute for Health and Sport, Victoria University, Melbourne, VIC 3011, Australia.
  6. Shanie Landen: Centre for Endocrinology and Metabolism, Hudson Institute of Medical Research, Melbourne, VIC 3168, Australia.
  7. Macsue Jacques: Institute for Health and Sport, Victoria University, Melbourne, VIC 3011, Australia.
  8. Elizabeth Byrnes: PathWest, QEII Medical Centre, Perth, WA 6009, Australia.
  9. Nir Eynon: Australian Regenerative Medicine Institute, Monash University, Clayton, VIC 3168, Australia.
  10. Marc Sim: Nutrition & Health Innovation Research Institute, Edith Cowan University, Joondalup, WA 6027, Australia.
  11. Joshua R Lewis: Nutrition & Health Innovation Research Institute, Edith Cowan University, Joondalup, WA 6027, Australia. ORCID
  12. Itamar Levinger: Institute for Health and Sport, Victoria University, Melbourne, VIC 3011, Australia. ORCID

Abstract

Lipocalin-2 (LCN2), a hormone produced by adipocytes, osteoblasts, and renal tubular cells, is implicated in age-related diseases, including cardio-metabolic disease. To understand the role LCN2 may play in pathological states, we first need to elucidate the relationship between circulating LCN2 with indices of cardio-metabolic health during "normal" aging. This study examined the relationship between serum levels of LCN2, age, and cardio-metabolic measures across the adult lifespan in males and females. We conducted a pooled cohort analysis including 124 community-dwelling males (���=���52) and females (���=���72) (age 20-87 yr, median BMI 25.92 [23.04, 29.81] kg/m). Serum LCN2 was analyzed using a two-step chemiluminescent microparticle monoclonal immunoassay. The relationship between LCN2 and age was evaluated by linear regression and cubic spline. Simple linear regressions were performed to investigate the relationship between LCN2 and the following variables: BMI, VO, serum glucose, and body composition (DXA). For every 1 yr increase in age, LCN2 levels were 0.26 mg/L higher ( =���.007, 95% CI [0.07, 0.45]). Each 1 unit increase in BMI (kg/m) was associated with 0.88 mg/L higher LCN2 levels ( =���.027, [0.10, 1.66]) and each 1 unit increase in VO (mL/kg/min) was associated with 0.38 mg/L lower LCN2 ( =���.003, [-0.63, -0.13]).There was no significant relationship between LCN2 and sex, glucose levels or body composition (all  >���.05). LCN2 increased linearly across the adult lifespan while it decreased as fitness level increased. Future research should build on these findings to determine whether LCN2 can be used as a biomarker for chronic disease and if exercise can mitigate age-related disease associated with LCN2 changes.

Keywords

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Word Cloud

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