Sleep Patterns and Dysfunctions in Children with Learning Problems

ANNALS ACADEMY OF MEDICINE SINGAPORE4511507-51

Perspectives on Palliative Care Among Duchenne Muscular Dystrophy Patients and Their Families in Singapore

10.47102/annals-acadmedsg.2019163ANNALS ACADEMY OF MEDICINE SINGAPORE49272-7

Simultaneous Screening of the FRAXA and FRAXE Loci for Rapid Detection of FMR1 CGG and/or AFF2 CCG Repeat Expansions by Triplet-Primed PCR

10.1016/j.jmoldx.2021.04.015JOURNAL OF MOLECULAR DIAGNOSTICS238941-95

Mitochondrial oxidative capacity and NAD biosynthesis are reduced in human sarcopenia across ethnicities

The causes of impaired skeletal muscle mass and strength during aging are well-studied in healthy populations. Less is known on pathological age-related muscle wasting and weakness termed sarcopenia, which directly impacts physical autonomy and survival. Here, we compare genome-wide transcriptional changes of sarcopenia versus age-matched controls in muscle biopsies from 119 older men from Singapore, Hertfordshire UK and Jamaica. Individuals with sarcopenia reproducibly demonstrate a prominent transcriptional signature of mitochondrial bioenergetic dysfunction in skeletal muscle, with low PGC-1α/ERRα signalling, and downregulation of oxidative phosphorylation and mitochondrial proteostasis genes. These changes translate functionally into fewer mitochondria, reduced mitochondrial respiratory complex expression and activity, and low NAD+ levels through perturbed NAD+ biosynthesis and salvage in sarcopenic muscle. We provide an integrated molecular profile of human sarcopenia across ethnicities, demonstrating a fundamental role of altered mitochondrial metabolism in the pathological loss of skeletal muscle mass and function in older people