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Cardiac troponin T is elevated and increases longitudinally in ALS patients

Kläppe, U. (author)
Karolinska Institutet
Chamoun, S. (author)
Shen, Q. (author)
Karolinska Institutet
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Finn, A. (author)
Evertsson, B. (author)
Zetterberg, Henrik, 1973 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi,Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry
Blennow, Kaj, 1958 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi,Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry
Press, R. (author)
Karolinska Institutet
Samuelsson, K. (author)
Karolinska Institutet
Månberg, Anna, 1985- (author)
KTH,Affinitets-proteomik
Fang, F. (author)
Karolinska Institutet
Ingre, C. (author)
Karolinska Institutet
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 (creator_code:org_t)
2021-06-21
2022
English.
In: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. - : Taylor and Francis Ltd.. - 2167-8421 .- 2167-9223. ; 23:1-2, s. 58-65
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Objective: To test whether high-sensitivity cardiac troponin T (hs-cTnT) could act as a diagnostic or prognostic biomarker in ALS, comparing hs-cTnT to neurofilament light (NfL). Methods: We performed a case-control study, including 150 ALS patients, 28 ALS mimics, and 108 healthy controls, and a follow-up study of the ALS patients, during 2014–2020 in Stockholm, Sweden. We compared concentrations of hs-cTnT in plasma and NfL in the cerebrospinal fluid between cases and controls. To evaluate the diagnostic performance, we calculated the area under the curve (AUC). Hazard ratios (HRs) were estimated from Cox models to assess associations between hs-cTnT and NfL at ALS diagnosis and risk of death. The longitudinal analysis measured changes of hs-cTnT and NfL since ALS diagnosis. Results: We noted higher levels of hs-cTnT in ALS patients (median: 16.5 ng/L) than in ALS mimics (11 ng/L) and healthy controls (6 ng/L). Both hs-cTnT and NfL could distinguish ALS patients from ALS mimics, with higher AUC noted for NfL (AUC 0.88; 95%CI 0.79–0.97). Disease progression correlated weakly with hs-cTnT (Pearson’s r = 0.18, p = 0.04) and moderately with NfL (Pearson’s r = 0.41, p < 0.001). Shorter survival was associated with higher levels of NfL at diagnosis (HR 1.08, 95%CI 1.04–1.11), but not hs-cTnT. hs-cTnT increased (12.61 ng/L per year, 95%CI 7.14–18.06) whereas NfL decreased longitudinally since ALS diagnosis. Conclusions: NfL is a stronger diagnostic and prognostic biomarker than hs-cTnT for ALS. However, hs-cTnT might constitute a disease progression biomarker as it increases longitudinally. The underlying causes for this increase need to be investigated. 

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

Keyword

amyotrophic lateral sclerosis
cardiac troponin T
Case-control study
follow-up study
neurofilament proteins
neurofilament protein
troponin T
adult
aged
Amyotrophic Lateral Sclerosis Functional Rating Scale
area under the curve
Article
body mass
case control study
cerebrospinal fluid
cohort analysis
comparative study
controlled study
diagnostic test accuracy study
disease exacerbation
enzyme linked immunosorbent assay
female
follow up
genetic risk
human
human tissue
longitudinal study
major clinical study
male
Case-control study
follow-up study
amyotrophic lateral sclerosis
cardiac troponin T
neurofilament proteins
amyotrophic-lateral-sclerosis
inclusion-body myositis
prognostic
biomarker
cardiomyopathy
neurofilaments
diagnosis
heart
Neurosciences & Neurology

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art (subject category)

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