TY - JOUR
T1 - IFN production ability and healthy ageing
T2 - Mixed model analysis of a 24 year longitudinal study in Japan
AU - Uno, Kazuko
AU - Yagi, Katsumi
AU - Yoshimori, Masayo
AU - Tanigawa, Mari
AU - Yoshikawa, Toshikazu
AU - Fujita, Setsuya
PY - 2013
Y1 - 2013
N2 - Objective: To track changes in interferon (IFN) production in healthy individuals to shed light on the effect these changes have on the course of healthy ageing. Design: Study is based on data that were collected over 24 years from a cohort of individuals whose IFN-α production was quantified as a part of their annual routine health check-up. Setting: All individuals in this study underwent regular health check-ups at Louis Pasteur Center for Medical Research. Participants: 295 healthy individuals (159 males and 136 females) without a history of cancer, autoimmune diseases and hepatitis C virus (HCV) whose IFN-α production was quantified more than five times within 24 years were selected. Finally, 29 males and 4 females whose IFN-α production was quantified more than 25 times were selected and their data were analysed using a mixed model. Main outcome measures: HVJ stimulated IFN-α production was quantified. Healthy individual's periodical log transformed IFN-α values (y) were plotted versus age (x) and fitted to linear (y=mx+n) and quadratic formula (y=ax2+bx+c) expressions to reveal changes in the IFN-α production in these healthy individuals. Results: The linear expression showed that log (IFN-α) had a slight tendency to decline (3% over 10 years). However, the quadratic formula analysis showed the quadratic expression to be more positive than negative (a concave U-shaped pattern) which means that individuals' once declining IFN production recovered as they aged. Conclusions: Although we observed a marginal decline in IFN-α production, we also observed that IFN production recovered even in individuals in their mid50s to early 60s. These results combined with our previous cross-sectional studies of patients with various diseases suggest that in healthy individuals, the impairment of IFN production is triggered more by the onset of disease (notwithstanding the cause) rather than by ageing.
AB - Objective: To track changes in interferon (IFN) production in healthy individuals to shed light on the effect these changes have on the course of healthy ageing. Design: Study is based on data that were collected over 24 years from a cohort of individuals whose IFN-α production was quantified as a part of their annual routine health check-up. Setting: All individuals in this study underwent regular health check-ups at Louis Pasteur Center for Medical Research. Participants: 295 healthy individuals (159 males and 136 females) without a history of cancer, autoimmune diseases and hepatitis C virus (HCV) whose IFN-α production was quantified more than five times within 24 years were selected. Finally, 29 males and 4 females whose IFN-α production was quantified more than 25 times were selected and their data were analysed using a mixed model. Main outcome measures: HVJ stimulated IFN-α production was quantified. Healthy individual's periodical log transformed IFN-α values (y) were plotted versus age (x) and fitted to linear (y=mx+n) and quadratic formula (y=ax2+bx+c) expressions to reveal changes in the IFN-α production in these healthy individuals. Results: The linear expression showed that log (IFN-α) had a slight tendency to decline (3% over 10 years). However, the quadratic formula analysis showed the quadratic expression to be more positive than negative (a concave U-shaped pattern) which means that individuals' once declining IFN production recovered as they aged. Conclusions: Although we observed a marginal decline in IFN-α production, we also observed that IFN production recovered even in individuals in their mid50s to early 60s. These results combined with our previous cross-sectional studies of patients with various diseases suggest that in healthy individuals, the impairment of IFN production is triggered more by the onset of disease (notwithstanding the cause) rather than by ageing.
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U2 - 10.1136/bmjopen-2012-002113
DO - 10.1136/bmjopen-2012-002113
M3 - Article
C2 - 23315513
AN - SCOPUS:84873420504
SN - 2044-6055
VL - 3
JO - BMJ open
JF - BMJ open
IS - 1
M1 - A35
ER -