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DOI 10.1097/mnm.0000000000001343

Медицинская библиотека · Nuclear medicine communications · 2021

Sex difference in cerebral blood flow and cerebral glucose metabolism: an activation-likelihood estimation meta-analysis.

Shin Seunghyeon, Kim Keunyoung, Nam Hyun-Yeol, Kim In Joo, Pak Kyoungjune

СтатьяМетаанализПеревод пока не подготовлен

Аннотация

OBJECTIVES

Sex differences exist in a variety of aspects including neurochemicals as well as behavioral traits of cognition, language, and aggression. We performed a meta-analysis of studies using a coordinate-based technique of activation-likelihood estimation (ALE) to identify the pooled estimated effect of sex difference.

METHODS

We performed a systematic search of MEDLINE and EMBASE for English-language publications using the keywords of 'positron emission tomography (PET)', 'single-photon emission computed tomography (SPECT)', and 'sex'. A threshold of uncorrected P < 0.001 (minimum volume of 200 mm3) was applied to the resulting ALE map.

RESULTS

Cerebral blood flow (CBF) in right precuneus, left superior temporal gyrus, left inferior temporal, left inferior frontal gyrus, right cerebellar tonsil, and right middle temporal gyrus was higher in females than males. CBF in left anterior cingulate was higher in males than females. Whereas, the cerebral metabolic rate for glucose (CMRglu) in left thalamus, left cingulate gyrus, right inferior parietal lobule, left medial frontal gyrus, right middle frontal gyrus, right midbrain, and left inferior parietal lobule was higher in females than males. However, there was no brain region that showed higher CMRglu in males than females.

CONCLUSION

Regional CBF and CMRglu from PET and SPECT showed the difference between males and females.

Для цитирования: Shin Seunghyeon, Kim Keunyoung, Nam Hyun-Yeol, Kim In Joo, Pak Kyoungjune. Sex difference in cerebral blood flow and cerebral glucose metabolism: an activation-likelihood estimation meta-analysis.. Nuclear medicine communications. 2021. DOI: 10.1097/mnm.0000000000001343.

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