Showing posts with label Hr. Show all posts
Showing posts with label Hr. Show all posts

Medial Temporal Lobe indices: Concept & Description


The recent focus on biomarkers in the diagnosis of Alzheimer's disease (AD) and its prodromal stage have created a need to translate research findings into tools for use in everyday clinical practice. Although AD and mild cognitive impairment (MCI) are commonly diagnosed using sets of clinical criteria, MRI findings may aid the clinical diagnosis, and may predict clinical progression. In AD, the medial temporal lobe (MTL) gets atrophied out of proportion to other brain areas in comparison to healthy age-matched controls and this fact may be used to ease the diagnosis. Indeed, the new research criteria have recently been proposed for AD, and MCI that incorporate (disproportionate) medial temporal lobe or hippocampal atrophy on MRI as one of the supportive features.

Age-associated differences are detected in the  MTL with an acceleration of Medial Temporal Lobe Atrophy (MTA) starting around 72 years of age in healthy people (read more). However, these changes are modest and their rate of progression over time is relatively slow with a mean rate of about 1.6% per year. Accelerated MTA is a consistent finding in AD and MCI with rates of about 2.8% in stable MCI, 3.7% in MCI transitioning to AD (MCI progressors), and up to 4.0% in AD. Frontotemporal dementia may also lead to MTA, but in a different pattern: frontotemporal dementia and semantic dementia show atrophy in the anterior portion of the hippocampus, and in semantic dementia the atrophy is asymmetrical, with the left hippocampus being affected more severely. No significant hippocampal atrophy is detected in non-fluent progressive aphasia. Other diseases such as dementia with Lewy bodies do not show MTA or it is much milder.

In contrast to MTA, ventricular enlargement (body of lateral ventricles) in old people lacks specificity, representing a measure of global brain atrophy due to aging or any neurodegenerative disorder. Ventricular enlargement  correlates with decline in cognitive performance and with cerebrospinal fluid pathologic markers of AD and several studied have assessed different methods based on the lateral ventricles measurements as AD biomarkers. However, it is well known that ventricular enlargement is a measure of global brain atrophy and is strongly associated with aging both in healthy and diseased people. In addition, almost any neurodegenerative disorder affecting the brain hemispheres leads to some degree of ventricular enlargement, including Parkinson’s disease, Frontotemporal Dementia, Lewy-Bodies Dementia and Corticobasal Degeneration and so do some psychiatric conditions. Thus, it is interesting to compare measures indicative of atrophy in the MTL with measures indicative of global brain atrophy. I propose the next indices, that allow us to interpret result of atrophy measures easier:

Planimetry methods consist in measuring the area of regions of interest (ROI). The areas of several ROI can be compared using ratios and indices. The Medial Temporal-Lobe Atrophy index (MTAi), is a simple method for measuring the relative extent of atrophy in the MTL in relation to the global brain atrophy. This 2D-method consists on calculating a ratio using the area of 3 regions traced manually on one single coronal MRI slide at the level of the interpeduncular fossa: 1. the medial temporal lobe region (A); 2. the parenchyma within the medial temporal region, that includes the hippocampus and the parahippocampal gyrus -the fimbria taenia and plexus choroideus were excluded- (B); and 3. the body of the ipsilateral lateral ventricle (C). Therefrom we can compute the “2D-Medial Temporal Atrophy” (2D-MTA=A-B) that represents absolute atrophy of the MTL; and the ratio “Medial Temporal Atrophy index”  (MTAi = (A-B) x10 / C) that represents relative atrophy of the MTL. The MTAi is suitable to assess the asymmetry of relative MTA within a subject. High asymmetry is typical of some types of FTLD. However, as there is important interindividual variability in the size of the lateral ventricles, this index is not recommended for comparing subjects but to track the progression in a given subject over time. Indeed, if we have 2 MRI studies from different times (1= first one, 2=second one), we can also compute the yearly rate of MTA (yrMTA)  as follows: yrMTA=(A2-B2)-(A1-B1) x 1200 / (#months between MRI studies) and the yearly rate of relative MTA (yrRMTA) as follows: yrRMTA=(A2-B2)-(A1-B1) x 1200 / (C2-C1) x (#months between MRI studies). High values are suggestive of "disproportionated" MTA in relation to the extent of global brain atrophy, and therefore the pattern of atrophy matches the expected in typical AD.

Volumetric methods are more sophisticated. The Medial Temporal-Lobe ratio (MTLr) compares the volume of the MTL with the whole hemispheric volume. To find out the MTLr we need 1. the volume of the hippocampus (A); the volume of the parahippocampal gyrus (B); 3. the volume of the whole brain hemisphere (C). We can compute the ratio “Medial Temporal Lobe ratio” as follows: MTLr = (A+B)^2 / C.  Low values are suggestive of MTL atrophy, and therefore the pattern of atrophy matches the expected in typical AD.
If we have 2 MRI studies from different times (1= first one, 2=second one), we can also compute the yearly rate of MTL atrophy (yrMTL) =(A1+B1)-(A2+B2) x 1200 / (#months between MRI studies) and the yearly rate of relative MTL atrophy as follows: (yrMTLr) =(A1+B1)-(A2+B2) x 1200 / (C2-C1) x (#months between MRI studies).

The Hippocampus ratio (Hr) compares the volume of the hippocampus with the whole hemispheric volume. To find out the HAr we need 1. the volume of the hippocampus (A); 2. the volume of the ipsilateral brain hemisphere (B). We can compute the ratio “Hippocampus ratio” as follows: HAr= A^2 / B. Low values are suggestive of hippocampus atrophy, and therefore the pattern of atrophy matches the expected in typical AD.
If we have 2 MRI studies from different times (1= first one, 2=second one), we can also compute the yearly rate of Hippocampus Atrophy as follows: (yrHA)= (A1-A2) x 1200 / (#months between MRI studies) and the yearly rate of relative Hippocampus atrophy as follows: (yrHAr)=(A1-A2) x 1200 / (B1-B2) x (#months between MRI studies).

The Hippocampus-Ventricle index (HVi) is the addition of the volume of the hippocampus plus the tenth part of the volume of the the lateral ventricle. Then, to find out the HVi we need  1. the  normalized volume of the hippocampus (A); 2. the normalized volume of the the lateral ventricle (B). We can compute the ratio “Hippocampus-Ventricle index” as follows: HVi = A+(B/10). Low HVi values are suggestive of AD pathology in incipient stages, while high HVi values are suggestive of global brain atrophy due to aging or any neurodegenerative disease other than AD. Intermediate values are not informative.


Compares Parameters needed to calculate it Computing Interpretation
Temporal horn index (Ti) Volume of the temporal horn with the volume of the lateral ventricles Temporal horn volume (A) and the lateral ventricular volume (B) THi= A / B Low values are suggestive of MTL atrophy, and therefore the pattern of atrophy matches the pattern expected in typical AD
Medial Temporal-Lobe ratio (MTLr)  Volume of the MTL with the ipsilateral hemispheric volume The volume of the hippocampus (A); the volume of the parahippocampal gyrus (B); the volume of the whole brain hemisphere (C) MTLr = (A+B)2 / C Low values are suggestive of MTL atrophy, and therefore the pattern of atrophy matches the pattern expected in typical AD
Yearly rate of MTL atrophy (yrMTLA) Not an index A and B as in MTLr in 2 different MRI studies (yrMTL) = (A1+B1) - (A2+B2) × 1200 / (# mo between MRI studies)  High values are expected in typical AD
Yearly rate of relative MTL atrophy (yrRMTLA) Rate of atrophy of the MTL with the rate of enlargement of the ipsilateral lateral ventricles A, B and C as in MTLr in 2 different MRI studies yrRMTA = (A1+B1)-(A2+B2) × 1200 / (C2-C1) × (# mo between MRI studies) High values are expected in early typical AD
Hippocampus ratio (Hr) Volume of the hippocampus with the ipsilateral hemispheric volume The volume of the hippocampus (A); the volume of the ipsilateral brain hemisphere (B) Hr = A2 / B Low values are suggestive of hippocampus atrophy, and therefore the pattern of atrophy matches the pattern expected in typical AD
Yearly rate of Hippocampus Atrophy (yrHA) Not an index A as in Hr in 2 different MRI studies (yrHA) = (A1-A2) × 1200 / (# mo between MRI studies)  High values are expected in typical AD
Yearly rate of relative Hippocampus Atrophy (yrRHA) Rate of atrophy of the hippocampus with the rate of atrophy of the ipsilateral hemisphere A and B as in Hr in 2 different MRI studies yrRHA = (A1-A2) × 1200 / (B1-B2) × (# mo between MRI studies) High values are expected in early typical AD
Hippocampus-Ventricle index (HVi) Addition of the volume of the hippocampus plus the 10th part of the volume of the lateral ventricle Normalized volume of the hippocampus (A); normalized volume of the lateral ventricle (B) HVi = A + (B/10) Low HVi values are suggestive of AD pathology in incipient stages; high HVi values are suggestive of global brain atrophy due to aging or any neurodegenerative disease other than AD
Volumetric indices for comparing the extent/rate of atrophy in the medial temporal lobe with the extent/rate of global brain atrophy (full text).