bims-tyki2d Biomed News
on Thymidine kinase 2 deficiency
Issue of 2026–06–21
eight papers selected by
Zoya Panahloo, UCB



  1. Brain Commun. 2026 ;8(3): fcag201
      Thymidine kinase 2 deficiency (TK2d) (MIM 609560) is an ultra-rare, autosomal recessive mitochondrial myopathy caused by TK2 variants, leading to mitochondrial DNA depletion and/or multiple deletions. People with thymidine kinase 2 deficiency experience progressive myopathy, bulbar weakness and respiratory insufficiency, often losing the ability to walk, eat and breathe independently. Doxecitine and doxribtimine represents the first approved treatment for patients with thymidine kinase 2 deficiency with age of symptom onset ≤12 years by the US Food and Drug Administration and the European Medicines Agency; previously, disease management was limited to supportive care. We investigated the efficacy and safety of pyrimidine nucleos(t)ide therapy in thymidine kinase 2 deficiency. Patients treated with pyrimidine nucleos(t)ides were pooled from retrospective (NCT03701568, NCT05017818) and prospective (NCT03845712) studies and company-supported Expanded Access Programs. Untreated patients were pooled from literature reviews and a retrospective chart review study (NCT05017818). Patient subgroups were stratified by age of thymidine kinase 2 deficiency symptom onset (≤12 years and >12 years). The primary outcome was survival in 50th-percentile matched pairs of treated and untreated patients. Other outcomes included status of developmental motor milestones, ventilatory and feeding tube support, and safety. In total, 218 patients were included (treated: 104; untreated: 114). Baseline demographics and characteristics were comparable between subgroups. Most patients had an age of symptom onset ≤12 years [treated: 82/104 (78.8%); untreated: 93/114 (81.6%)]. In the age-of-symptom-onset-≤12-years subgroup, restricted mean survival time (95% confidence interval) was 29.2 (28.2, 30.3) years over the 30 years after symptom onset for treated patients and 14.4 (11.1, 17.6) years for untreated patients. Loss of ≥1 acquired motor milestone was more frequent before treatment start than after. Substantially more patients regained ≥1 lost motor milestone after treatment start than before. Ventilatory and feeding support were used across all age-of-symptom-onset subgroups, but some patients reduced or discontinued support after starting treatment and fewer patients initiated support after treatment start than before. Most treatment-emergent adverse events (TEAEs) did not lead to discontinuation. The most frequent TEAE was diarrhoea [43/50 patients (86.0%)], which was generally mild or moderate and resolved with dose reduction. Serious TEAEs occurred in 28/50 patients (56.0%); few were considered to be drug related [4/50 (8.0%)]. In total, 3/67 patients (4.5%) experienced a fatal serious TEAE, which were not considered to be drug related. These findings indicate that pyrimidine nucleos(t)ide therapy improves survival and functional outcomes in people with thymidine kinase 2 deficiency, especially those with age of symptom onset ≤12 years, and has an acceptable safety profile.
    Keywords:  mitochondrial myopathy; pyrimidine nucleos(t)ide therapy; survival; thymidine kinase 2 deficiency; treatment efficacy
    DOI:  https://doi.org/10.1093/braincomms/fcag201
  2. Brain Commun. 2026 ;8(3): fcag200
      Thymidine kinase 2 deficiency (MIM 609560) is an ultra-rare, autosomal recessive mitochondrial disease, resulting in progressive myopathy, respiratory insufficiency and increased risk of early death. Doxecitine and doxribtimine represents the first approved treatment for thymidine kinase 2 deficiency in the USA and the EU; previously, management was restricted to supportive care. The overall understanding of the natural history of thymidine kinase 2 deficiency is limited. Our study describes the baseline characteristics, survival and disease progression of untreated patients with thymidine kinase 2 deficiency as part of one of the largest international datasets to date. Data from individuals with thymidine kinase 2 deficiency identified through the review of published literature and a retrospective chart review study (NCT05017818) were pooled with pretreatment data from patients later treated with pyrimidine nucleos(t)ides (NCT03701568; NCT03845712; NCT05017818; company-supported Expanded Access Programs). Subgroups were stratified by age of thymidine kinase 2 deficiency symptom onset (≤12 years and >12 years). Key outcomes measured included survival, developmental motor milestone attainment, loss, regain and use of ventilatory and feeding support. In total, 257 patients were included in the study. Most patients [n = 199 (77.4%)] had an age of symptom onset ≤12 years, while 49 (19.1%) had an age of symptom onset >12 years; age of onset was missing for 9 (3.5%). Kaplan-Meier survival analyses estimated that the median time (95% confidence interval) from symptom onset to death was 2.6 (1.3, 6.4) years with age of symptom onset ≤12 years and 24.0 (16.0, not applicable) years with age of symptom onset >12 years. Loss of previously acquired motor milestones was observed across both subgroups, though most frequently in those with age of symptom onset ≤12 years [61/75 patients (81.3%) lost ≥1 motor milestone]. Spontaneous regain of lost motor milestones was rare [3/71 patients (4.2%), all with age of symptom onset ≤12 years]. Use of ventilatory support was observed for both subgroups [81/199 patients (40.7%) with age of symptom onset ≤12 years (missing data, n = 73); 23/49 patients (46.9%) with age of symptom onset >12 years (missing data, n = 11)]. Use of feeding tube support was also reported [28/199 patients (14.1%) with age of symptom onset ≤12 years (missing data, n = 121); 4/49 patients (8.2%) with age of symptom onset >12 years (missing data, n = 21)]. This study confirms the severe disease burden and high mortality associated with thymidine kinase 2 deficiency, underscoring the devastating impact on quality of life. This comprehensive dataset provides a valuable resource for informing clinical management and future therapeutic strategies.
    Keywords:  mitochondrial myopathy; motor milestones; natural history; survival; thymidine kinase 2 deficiency
    DOI:  https://doi.org/10.1093/braincomms/fcag200
  3. Clin Transl Sci. 2026 Jun;19(6): e70634
      Primary mitochondrial diseases (PMDs) result from genetic variants in nuclear DNA and mitochondrial DNA which commonly lead to aberrant oxidative phosphorylation. The clinical complexity, often attributed to the underlying genetics, includes several distinct syndromes (e.g., Barth syndrome; Pearson syndrome; Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes), some with overlapping symptoms. PMDs are highly heterogenous and affect multiple organs and tissues, prominently those with high energy demand such as muscle and neurologic tissues. Disease-modifying therapies for PMDs approved by the United States Food and Drug Administration are few and disease-specific, and treatment remains largely supportive in nature. The lack of robust biomarkers contributes to challenges associated with quantifying treatment responses in drug development. Recognizing this area of critical need, we sought to understand the landscape of molecular biomarkers that may inform treatment response, support clinical trials, and may be useful for regulatory decision-making. In this review, we assess the extent of evidence and challenges for each biomarker. We propose considerations for future biomarker development to measure treatment response and facilitate early drug development in PMDs by guiding dose selection and trial enrichment.
    DOI:  https://doi.org/10.1111/cts.70634
  4. J Genet Couns. 2026 Jun;35(3): e70248
      The profession of genetic counselor remains underdeveloped and unregulated in Ukraine, despite growing demand for genetics-related healthcare services and expanding access to genetic testing. In the absence of formally trained genetic counselors, core professional functions-including risk communication, psychosocial support, and patient education-are delivered inconsistently or assumed by medical geneticists and other healthcare providers. The current landscape of genetic services in Ukraine is examined through the lens of the genetic counseling profession, highlighting key challenges, including limited access to genetic services, excessive workloads among medical geneticists that compromise the quality of counseling, and a lack of formal professional recognition for genetic counselors. Existing educational opportunities and emerging initiatives aimed at developing genetic counseling training in Ukraine are briefly reviewed. Finally, the professional context for integrating genetic counselors into the healthcare system is outlined, and the priority areas requiring further development to support effective integration and patient-centered genetic care are summarized.
    Keywords:  Ukraine; genetic counseling; professional development; professional integration
    DOI:  https://doi.org/10.1002/jgc4.70248
  5. Front Public Health. 2026 ;14 1769908
       Background: Genomic Newborn Screening (gNBS) could transform neonatal healthcare by enabling early detection of genetic disorders, timely intervention, and improved health outcomes. This study assessed healthcare professionals' self-reported knowledge, attitudes, and challenges regarding expanded newborn genomic screening in Abu Dhabi, United Arab Emirates (UAE), and identified factors influencing its integration into neonatal healthcare.
    Methods: A cross-sectional survey was distributed to healthcare professionals across public and private facilities in Abu Dhabi, using random and snowball sampling. Data were analyzed using descriptive statistics, chi-square tests, and logistic regression to examine associations between gNBS self-reported knowledge, attitudes, and professional characteristics.
    Results: About 46% (95% CI: 40%-52%) of professionals demonstrated good self-reported knowledge of gNBS, with significantly higher awareness among those experienced in newborn screening and tandem mass spectrometry. While 70% supported expanding gNBS, key barriers included cost, lack of screening guidelines, and ethical concerns such as genetic privacy and psychological distress for families. Most participants (85%) supported upskilling nurses and midwives for cord blood collection. Additionally, severe combined immunodeficiency (SCID), Duchenne muscular dystrophy (DMD), and spinal muscular atrophy (SMA) were essential conditions for inclusion in expanded gNBS programs.
    Conclusion: Healthcare professionals in Abu Dhabi recognize the potential of gNBS but also acknowledge key implementation challenges. Advancing implementation requires training, policy development, and ethical considerations. Future efforts should prioritize cost-effectiveness evaluations, regulatory frameworks, and stakeholder engagement to support sustainable and equitable gNBS implementation in the UAE.
    Keywords:  United Arab Emirates; attitudes; ethical considerations; genomic literacy; healthcare professionals; newborn screening; tandem mass spectrometry
    DOI:  https://doi.org/10.3389/fpubh.2026.1769908
  6. Indian J Pediatr. 2026 Jun 16.
    Executive Committee of the Society for Indian Academy of Medical Genetics (SIAMG)
      Next-generation sequencing (NGS)-based tests are being increasingly employed by clinicians for obtaining a genetic diagnosis in individuals and families with possible genetic disorders. However, there is a significant disparity in the genomic knowledge and skills of the clinicians employing these tests for care and management of families with rare genetic disorders. Through the current document, the Society for Indian Academy of Medical Genetics (SIAMG) aims to provide guidance and consideration in terms of the type of tests available, their appropriate applications, and result interpretation in order to make judicious use of these tests for rare disease diagnosis.
    Keywords:  Genetic counseling; Next generation sequencing; Rare genetic disorders
    DOI:  https://doi.org/10.1007/s12098-026-06124-w
  7. Neurotherapeutics. 2026 Jun 15. pii: S1878-7479(26)00115-7. [Epub ahead of print]23(4): e00945
      We evaluated the safety and efficacy of enteral deoxycytidine/deoxythymidine combination therapy in treatment of POLG-related disorders, genetic mitochondrial diseases characterized by progressive neurological degeneration. A single-centre open-label phase II trial was conducted. Inclusion criteria included: age 3 months to 60 years, clinical diagnosis of POLG-related disorder, and biallelic pathogenic POLG variants. Participants received deoxycytidine/deoxythymidine initially at 100 mg/kg/day (50 mg/kg deoxycytidine and 50 mg/kg deoxythymidine), titrated to 400 mg/kg/day over three weeks. The current protocol is a 60-month treatment period with primary outcomes the Newcastle Mitochondrial Disease Scale sections I-III and serum growth differentiation factor 15. Secondary outcomes include quality of life questionnaires, seizure diary, EEG, and blood and urine laboratory tests assessing end organ function. Outcomes were assessed at baseline, 1-month, 2-month, 3-month, and 6-month timepoints, then every 6 months thereafter. Twenty-five individuals (14 male, 11 female; mean age 12.3 years) started deoxycytidine/deoxythymidine. Five died during the trial and five withdrew. The most common treatment-related adverse event was diarrhea. Newcastle Mitochondrial Disease Scale sections I-III score decreased (improved) from baseline at all timepoints from 1 month to 24 months (p < 0.05). Serum growth differentiation factor 15 significantly decreased (improved) from baseline at 1-month, 2-month, and 3-month timepoints (p < 0.05). Quality of life score improved at 3-month, 12-month, and 18-month timepoints (p < 0.05). In summary, our data suggest deoxycytidine/deoxythymidine is safe and effective for POLG-related disorders; however, further study is needed to clarify the therapeutic mechanism(s) so that the treatment can be refined and optimized.
    Keywords:  DNA polymerase gamma; Deoxynucleoside; Mitochondrial DNA depletion disorder; Mitochondrial disorder; POLG
    DOI:  https://doi.org/10.1016/j.neurot.2026.e00945
  8. Am J Hum Genet. 2026 Jun 15. pii: S0002-9297(26)00196-5. [Epub ahead of print]
      Artificial intelligence (AI) is rapidly reshaping genomic medicine, yet its benefits remain unevenly distributed due to the profound under-representation of African populations in genomic datasets and persistent legacies of mistrust. These structural gaps undermine model validity, amplify bias, and limit clinical utility across the world's most genetically diverse populations. Building trustworthy AI for genomics in African populations requires transparent and interpretable systems, equitable data generation led by African institutions, culturally grounded governance, and rigorous population-specific validation. Advancing these principles is essential to ensure that AI reduces, rather than reinforces, global genomic inequities.
    Keywords:  AI; Africa; genomics
    DOI:  https://doi.org/10.1016/j.ajhg.2026.05.009