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. 2025 Jan 9;20(Suppl 2):e090224. doi: 10.1002/alz.090224

Sex Differences in Amyloid PET in a Large, Real‐Life Sample from the Imaging Dementia‐Evidence for Amyloid Scanning (IDEAS) Study

Maison Abu Raya 1,, Ehud Zeltzer 2, Daniel R Schonhaut 2, Isabel Elaine Allen 3,4,5,6, Maria C Carrillo 7, Constantine Gatsonis 8, Lucy Hanna 8, Bruce E Hillner 9, Leo Iaccarino 10, Andrew March 11, Nidhi S Mundada 2, Jhony Alejandro Mejía‐Perez 12, Barry A Siegel 13, Charles Windon 2, Rachel A Whitmer 14, Renaud La Joie 10, Gil D Rabinovici 15
PMCID: PMC11714663  PMID: 39784259

Abstract

Background

Previous studies on sex differences in amyloid burden have shown inconsistent findings. We examined the effect of sex on amyloid‐PET outcomes in a large, real‐world, cohort of individuals with cognitive impairment.

Method

The IDEAS study evaluated the clinical utility of amyloid‐PET in 18,295 Medicare beneficiaries age ≥65 years with MCI or dementia. All scans were visually interpreted as positive or negative at each site by a local radiologist or nuclear medicine physician. A subset of 10,361 scans were centrally processed and quantified in Centiloids. We used multivariate logistic regression to calculate odds ratios of amyloid‐PET positivity (based on visual read) for males and females, adjusting for demographic and clinical risk factors. We used linear regression to assess the association between sex and amyloid burden quantified in Centiloids.

Result

Of 10,361 included individuals, 51% were females. Compared to males, females were slightly younger (75 versus 76 median age, p=0.008) and had higher rates of dementia (39.3% versus 35.2%, p<0.001). Rates of vascular risk factors were significantly higher in males than females, whereas females had significantly higher rates of history of depression and family history of AD. Females had higher rates of amyloid‐PET positivity than males (63% versus 59%, p<.001) and higher Centiloid values (median=48.7 versus 36.9, p<.01); see Figure 1 and Table 1 model 1. Sex differences remained significant in models adjusted for demographics and clinical risk factors (Table 1, models 2‐3). In an analysis that included only individuals with visually positive amyloid‐PET, females exhibited higher Centiloid values than males (Table 1 multivariable linear models). In amyloid‐positive individuals, we found a significant interaction between sex and age, with greatest sex differences in amyloid burden found in the youngest females (Figure 2A). We also found a significant interaction between sex and race, with greatest differences found in Black females vs. males (Figure 2B).

Conclusion

Females with cognitive impairment exhibited a higher frequency of amyloid‐PET positivity and higher amyloid burden. Our findings shed light on sex‐specific biological and potential sociocultural differences in Alzheimer's disease pathology.


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