General Information:
Id: | 7,412 |
Diseases: |
Alzheimer disease
- [OMIM]
|
Homo sapiens | |
review | |
Reference: | Riedel BC et al.(2016) Age, APOE and sex: Triad of risk of Alzheimers disease J. Steroid Biochem. Mol. Biol. 160: 134-147 [PMID: 26969397] |
Interaction Information:
Comment | Age, apolipoprotein E4 (APOE4) and chromosomal sex are well-established risk factors for late-onset Alzheimer's disease (LOAD; AD). Over 60% of persons with AD harbor at least one APOE-E4 allele. |
Formal Description Interaction-ID: 72681 |
|
Comment | The sex-based prevalence of AD is well documented with over 60% of persons with AD being female. Evidence indicates that the APOE-E4 risk for AD is greater in women than men, which is particularly evident in heterozygous women carrying one APOE-E4 allele. Paradoxically, men homozygous for APOE-E4 are reported to be at greater risk for mild cognitive impairment and AD. |
Formal Description Interaction-ID: 73892 |
phenotype sex, female increases_activity of disease |
Comment | The sex-based prevalence of AD is well documented with over 60% of persons with AD being female. Evidence indicates that the APOE-E4 risk for AD is greater in women than men, which is particularly evident in heterozygous women carrying one APOE-E4 allele. Paradoxically, men homozygous for APOE-E4 are reported to be at greater risk for mild cognitive impairment and AD. |
Formal Description Interaction-ID: 73895 |
phenotype sex, male increases_activity of disease |
Comment | The sex-based prevalence of AD is well documented with over 60% of persons with AD being female. Evidence indicates that the APOE-E4 risk for AD is greater in women than men, which is particularly evident in heterozygous women carrying one APOE-E4 allele. Paradoxically, men homozygous for APOE-E4 are reported to be at greater risk for mild cognitive impairment and AD. |
Formal Description Interaction-ID: 73897 |
phenotype sex, male increases_activity of phenotype mild cognitive impairment |