The phrase "abnormal aging" is correct and usable in written English.
It can be used in contexts discussing age-related changes that deviate from typical aging processes, often in medical or psychological discussions.
Example: "Research has shown that individuals with certain genetic markers may experience abnormal aging, leading to earlier onset of age-related diseases."
Alternatives: "atypical aging" or "irregular aging".
Our findings showcase the importance of sensory profiles in determining multisensory benefits in healthy and abnormal aging.
The pattern of sensory dominance shifted with healthy and abnormal aging to favour a propensity of auditory-dominant behaviour (i.e., detecting sounds faster than flashes).
While information processing takes place in environments commonly multisensory in nature, the existing literature is currently unclear as to how healthy and abnormal aging influence this processing.
The efficacy of the cholinergic system declines in healthy aging, and is disrupted by abnormal aging processes, such as those underlying MCI or AD17.
The researchers wanted to understand how and when reasoning and memory change over the life span as a basis for distinguishing normal from abnormal aging.
The causes of the disease are complex and multifactorial and include genetic disposition, lifestyle choices, abnormal aging processes, and alterations in metabolic processes.
Endothelial cell loss can be accelerated via mechanical trauma or abnormal age-related endothelial cell death (called Fuchs endothelial dystrophy).
Moreover, CHR patients who later converted to overt psychosis showed a distinct pattern of abnormal age-associated activation in the frontal cortex relative to controls, while non-converters showed a more diffuse posterior pattern.
As ferritin, an acute phase reactant, may be elevated during co-morbid infection(s), iron deficiency (ID) was defined as ≥2 abnormal age-corrected iron parameters (iron, ferritin, transferrin and transferrin saturation).
Furthermore, in this study ID was defined on the basis of ≥2 abnormal age-corrected iron parameters, assisting in better identification of ID in the presence of infection and inflammation [31].
The findings of this study support other research that finds value in cognitive training for older adults, including those experiencing both normal and abnormal age-related changes in cognition with aging.
