Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2017 Jul 24;7(1):6220.
doi: 10.1038/s41598-017-06138-7.

Functional correlates of TSH, fT3 and fT4 in Alzheimer disease: a F-18 FDG PET/CT study

Affiliations

Functional correlates of TSH, fT3 and fT4 in Alzheimer disease: a F-18 FDG PET/CT study

Agostino Chiaravalloti et al. Sci Rep. .

Abstract

The present study was aimed to investigate the relationships between thyroid stimulating hormone (TSH), freeT3 (fT3) and freeT4 (fT4) and brain glucose consumption as detectable by means of 2-deoxy-2-(F-18) fluoro-D-glucose (F-18 FDG) Positron Emission Tomography/Computed Tomography (PET/CT) in a selected population with Alzheimer disease (AD). We evaluated 87 subjects (37 males and 50 females, mean age 70 (±6) years old) with AD. All of them were subjected to TSH, fT3 and fT4 assay and to cerebrospinal fluid amyloid (Aβ1-42) and tau [phosphorylated-tau (p-tau) and total-tau (t-tau)] assay prior PET/CT examination. Values for TSH, fT3 and fT4 were in the normal range. The relationships were evaluated by means of statistical parametric mapping (SPM8) using age, sex, MMSE, scholarship and CSF values of amyloid and tau as covariates. We found a significant positive correlation between TSH values and cortical glucose consumption in a wide portion of the anterior cingulate cortex bilaterally (BA32) and left frontal lobe (BA25) (p FWE-corr <0.001; p FDRcorr <0.000; cluster extent 66950). No significant relationships were found between cortical F-18 FDG uptake and T3 and T4 serum levels. The results of our study suggest that a cortical dysfunction in anterior cingulate and frontal lobes may affect serum values of TSH in AD patients.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Figure 1
Figure 1
3D rendering of data presented in Table 3 in (a) showing the positive correlation between TSH and brain glucose consumption in left anterior cingulate cortex (<) and medial frontal gyrus (*) and in the right anterior cingulate cortex (b, >). Threshold P < 0.01 corrected for multiple comparisons with false discovery rate at the voxel level. Coordinate and other regional details are presented in Table 3.
Figure 2
Figure 2
T1 magnetic resonance imaging superimposition showing the significant (positive) relationship between cortical activity in BA25 and that of the region corresponding to the hypothalamus. Since cluster was large as compared to the anatomical region here represented, for illustrative purposes a mask with WFU pickatlas was generated. Coordinates are shown in Table 4.

Similar articles

Cited by

References

    1. Selkoe DJ. Deciphering the genesis and fate of amyloid beta-protein yields novel therapies for Alzheimer disease. J Clin Invest. 2002;110:1375–1381. doi: 10.1172/JCI0216783. - DOI - PMC - PubMed
    1. Perl DP. Neuropathology of Alzheimer’s disease and related disorders. Neurol Clin. 2000;18:847–864. doi: 10.1016/S0733-8619(05)70229-2. - DOI - PubMed
    1. Stromer T, Serpell LC. Structure and morphology of the Alzheimer’s amyloid fibril. Microsc Res Tech. 2005;67:210–217. doi: 10.1002/jemt.20190. - DOI - PubMed
    1. Ashford JW, Soultanian NS, Zhang SX, Geddes JW. Neuropil threads are collinear with MAP2 immunostaining in neuronal dendrites of Alzheimer brain. J Neuropathol Exp Neurol. 1998;57:972–978. doi: 10.1097/00005072-199810000-00009. - DOI - PubMed
    1. Fagan AM, et al. Cerebrospinal Fluid tau/-Amyloid42 Ratio as a Prediction of Cognitive Decline in Nondemented Older Adults. Arch Neurol. 2007;64:343–349. doi: 10.1001/archneur.64.3.noc60123. - DOI - PubMed