Telomere length is associated with growth in children in rural Bangladesh

Audrie Lin, Andrew N Mertens, Benjamin F Arnold, Sophia Tan, Jue Lin, Christine P Stewart, Alan E Hubbard, Shahjahan Ali, Jade Benjamin-Chung, Abul K Shoab, Md Ziaur Rahman, Syeda L Famida, Md Saheen Hossen, Palash Mutsuddi, Salma Akther, Mahbubur Rahman, Leanne Unicomb, Ruchira Tabassum Naved, Md Mahfuz Al Mamun, Kausar Parvin, Firdaus S Dhabhar, Patricia Kariger, Lia Ch Fernald, Stephen P Luby, John M Colford Jr, Audrie Lin, Andrew N Mertens, Benjamin F Arnold, Sophia Tan, Jue Lin, Christine P Stewart, Alan E Hubbard, Shahjahan Ali, Jade Benjamin-Chung, Abul K Shoab, Md Ziaur Rahman, Syeda L Famida, Md Saheen Hossen, Palash Mutsuddi, Salma Akther, Mahbubur Rahman, Leanne Unicomb, Ruchira Tabassum Naved, Md Mahfuz Al Mamun, Kausar Parvin, Firdaus S Dhabhar, Patricia Kariger, Lia Ch Fernald, Stephen P Luby, John M Colford Jr

Abstract

Background: Previously, we demonstrated that a water, sanitation, handwashing, and nutritional intervention improved linear growth and was unexpectedly associated with shortened childhood telomere length (TL) (Lin et al., 2017). Here, we assessed the association between TL and growth.

Methods: We measured relative TL in whole blood from 713 children. We reported differences between the 10th percentile and 90th percentile of TL or change in TL distribution using generalized additive models, adjusted for potential confounders.

Results: In cross-sectional analyses, long TL was associated with a higher length-for-age Z score at age 1 year (0.23 SD adjusted difference in length-for-age Z score [95% CI 0.05, 0.42; FDR-corrected p-value = 0.01]). TL was not associated with other outcomes.

Conclusions: Consistent with the metabolic telomere attrition hypothesis, our previous trial findings support an adaptive role for telomere attrition, whereby active TL regulation is employed as a strategy to address 'emergency states' with increased energy requirements such as rapid growth during the first year of life. Although short periods of active telomere attrition may be essential to promote growth, this study suggests that a longer overall initial TL setting in the first 2 years of life could signal increased resilience against future telomere erosion events and healthy growth trajectories.

Funding: Funded by the Bill and Melinda Gates Foundation.

Clinical trial number: NCT01590095.

Keywords: child; developmental origins of health; disease; epidemiology; global health; growth; human; low-income; pediatric population; telomere length.

Conflict of interest statement

AL, CS, AH, SA, JB, AS, MR, SF, PM, SA, MR, LU, RN, KP, FD, PK, SL J.L. is a co-founder of Telomere Diagnostics Inc, a telomere measurement company. Assays and all other activity for the current report are, however, unrelated to this company. All other co-authors have no competing interests to declare. AM, BA, ST, JL, MH, MM, LF, JC No competing interests declared

© 2021, Lin et al.

Figures

Figure 1.. Diagram of participants at each…
Figure 1.. Diagram of participants at each phase of the telomere length and growth substudy within the WASH Benefits trial.
Figure 2.. Adjusted association between telomere length…
Figure 2.. Adjusted association between telomere length and growth.
Adjusted differences in mean anthropometry Z score between 10th and 90th percentile of telomere measure. LAZ = length-for-age Z score; WAZ = weight-for-age Z score; WLZ = weight-for-length Z score; HCZ = head circumference-for-age Z score.
Figure 2—figure supplement 1.. Association between telomere…
Figure 2—figure supplement 1.. Association between telomere length at Year 1 and concurrent and subsequent growth.
Spline curves of telomere length at Year 1 and anthropometric Z scores at Years 1 and 2, change in anthropometric Z scores, and growth velocity. T/S Ratio = unit for relative telomere length; LAZ = length-for-age Z score; WAZ = weight-for-age Z score; WLZ = weight-for-length Z score; HCZ = head circumference-for-age Z score.
Figure 2—figure supplement 2.. Association between telomere…
Figure 2—figure supplement 2.. Association between telomere length at Year 2 and concurrent growth.
Spline curves of telomere length at Year 2 and anthropometric Z scores at Year 2. T/S ratio = unit for relative telomere length; LAZ = length-for-age Z score; WAZ = weight-for-age Z score; WLZ = weight-for-length Z score; HCZ = head circumference-for-age Z score.
Figure 2—figure supplement 3.. Association between change…
Figure 2—figure supplement 3.. Association between change in telomere length between Years 1 and 2 and growth.
Spline curves of change in telomere length between Years 1 and 2 and anthropometric Z scores at Year 2, change in anthropometric Z scores, and growth velocity. T/S ratio = unit for relative telomere length; LAZ = length-for-age Z score; WAZ = weight-for-age Z score; WLZ = weight-for-length Z score; HCZ = head circumference-for-age Z score.
Figure 3.. Regression to the mean assessment:…
Figure 3.. Regression to the mean assessment: association between telomere length at Year 1 and change in telomere length between Years 1 and 2.
T/S ratio = unit for relative telomere length.
Figure 3—figure supplement 1.. Regression to the…
Figure 3—figure supplement 1.. Regression to the mean comparison of unadjusted association between change in telomere length and growth.
Unadjusted differences in mean anthropometry Z score between 10th and 90th percentile of change in telomere length between Years 1 and 2. Unadjusted associations corrected for the regression to the mean (RTM) effect using the equation in Verhulst et al., 2013. LAZ = length-for-age Z score; WAZ = weight-for-age Z score; WLZ = weight-for-length Z score; HCZ = head circumference-for-age Z score.
Figure 3—figure supplement 2.. Regression to the…
Figure 3—figure supplement 2.. Regression to the mean comparison of adjusted association between change in telomere length and growth.
Adjusted differences in mean anthropometry Z score between 10th and 90th percentile of change in telomere length between Years 1 and 2. Adjusted associations corrected for the regression to the mean (RTM) effect using the equation in Verhulst et al., 2013. LAZ = length-for-age Z score; WAZ = weight-for-age Z score; WLZ = weight-for-length Z score; HCZ = head circumference-for-age Z score. Adjusted for pre-specified covariates: Child age, child sex, birth order, prior child length and weight measurements from Year 1 (included in Year 2 outcomes only), season of measurement, time between anthropometry measurements (included in growth velocity and change in growth measurements between Year 1 and Year 2 outcomes only), caregiver-reported diarrhoea, mother’s age, mother’s height, mother’s education level, mother’s Center for Epidemiologic Studies Depression Scale Revised (CESD-R) score, mother’s Perceived Stress Scale score, mother’s lifetime exposure to physical, sexual, and emotional intimate partner violence, household food insecurity, number of children
All figures (8)

References

    1. Avila JT. Normal Adolescent Growth and Development, Reference Module in Biomedical Sciences. Amsterdam, Netherlands: Elsevier; 2021.
    1. Aviv A. Telomeres and human aging: Facts and fibs. Science of Aging Knowledge Environment. 2004;2004:e43. doi: 10.1126/sageke.2004.51.pe43.
    1. Aviv A, Hunt SC, Lin J, Cao X, Kimura M, Blackburn E. Impartial comparative analysis of measurement of leukocyte telomere length/dna content by southern Blots and QPCR. Nucleic Acids Research. 2011;39:e134. doi: 10.1093/nar/gkr634.
    1. Barker DJP. The origins of the developmental origins theory. Journal of Internal Medicine. 2007;261:412–417. doi: 10.1111/j.1365-2796.2007.01809.x.
    1. Berry DA, Eaton ML, Ekholm BP, Fox TL. Assessing differential drug effect. Biometrics. 1984;40:1109–1115. doi: 10.2307/2531162.
    1. Black RE, Victora CG, Walker SP, Bhutta ZA, Christian P, de Onis M, Ezzati M, Grantham-McGregor S, Katz J, Martorell R, Uauy R, Maternal and Child Nutrition Study Group Maternal and child undernutrition and overweight in low-income and middle-income countries. Lancet. 2013;382:427–451. doi: 10.1016/S0140-6736(13)60937-X.
    1. Black MM, Walker SP, Fernald LCH, Andersen CT, DiGirolamo AM, Lu C, McCoy DC, Fink G, Shawar YR, Shiffman J, Devercelli AE, Wodon QT, Vargas-Barón E, Grantham-McGregor S, Lancet Early Childhood Development Series Steering Committee Early childhood development coming of age: Science through the life course. Lancet. 2017;389:77–90. doi: 10.1016/S0140-6736(16)31389-7.
    1. Blackburn EH. Switching and signaling at the telomere. Cell. 2001;106:661–673. doi: 10.1016/s0092-8674(01)00492-5.
    1. Bosquet Enlow M, Kane-Grade F, De Vivo I, Petty CR, Nelson CA. Patterns of change in telomere length over the first three years of life in healthy children. Psychoneuroendocrinology. 2020;115:104602. doi: 10.1016/j.psyneuen.2020.104602.
    1. Broer L, Codd V, Nyholt DR, Deelen J, Mangino M, Willemsen G, Albrecht E, Amin N, Beekman M, de Geus EJC, Henders A, Nelson CP, Steves CJ, Wright MJ, de Craen AJM, Isaacs A, Matthews M, Moayyeri A, Montgomery GW, Oostra BA, Vink JM, Spector TD, Slagboom PE, Martin NG, Samani NJ, van Duijn CM, Boomsma DI. Meta-analysis of telomere length in 19,713 subjects reveals high heritability, stronger maternal inheritance and a paternal age effect. European Journal of Human Genetics. 2013;21:1163–1168. doi: 10.1038/ejhg.2012.303.
    1. Casagrande S, Hau M. Telomere attrition: Metabolic regulation and signalling function? Biology Letters. 2019;15:20180885. doi: 10.1098/rsbl.2018.0885.
    1. Cawthon RM. Telomere measurement by quantitative PCR. Nucleic Acids Research. 2002;30:e47. doi: 10.1093/nar/30.10.e47.
    1. Cawthon RM, Smith KR, O’Brien E, Sivatchenko A, Kerber RA. Association between telomere length in blood and mortality in people aged 60 years or older. Lancet. 2003;361:393–395. doi: 10.1016/S0140-6736(03)12384-7.
    1. Cogill, B. Anthropometric Indicators Measurement Guide. United States: Food and Nutritional Technical Assistance Project; 2003.
    1. Cohen S. Perceived Stress Scale. Mind Garden; 1994.
    1. Daniali L, Benetos A, Susser E, Kark JD, Labat C, Kimura M, Desai K, Granick M, Aviv A. Telomeres shorten at equivalent rates in somatic tissues of adults. Nature Communications. 2013;4:1597. doi: 10.1038/ncomms2602.
    1. de Onis M, Onyango AW, Van den Broeck J, Chumlea WC, Martorell R. Measurement and standardization protocols for anthropometry used in the construction of a new international growth reference. Food and Nutrition Bulletin. 2004;25:S27–S36. doi: 10.1177/15648265040251S104.
    1. de Onis M, Garza, C, O’nyango, A, Martorell, R. WHO Child Growth Standards based on length/height, weight and age. Acta Paediatrica. 2006;450:S5–S101. doi: 10.1111/j.1651-2227.2006.tb02378.x.
    1. Elwood N. Telomere biology of human hematopoietic stem cells. Cancer Control. 2004;11:77–85. doi: 10.1177/107327480401100214.
    1. Fitzpatrick AL, Kronmal RA, Gardner JP, Psaty BM, Jenny NS, Tracy RP, Walston J, Kimura M, Aviv A. Leukocyte telomere length and cardiovascular disease in the cardiovascular health study. American Journal of Epidemiology. 2007;165:14–21. doi: 10.1093/aje/kwj346.
    1. Humphrey JH. Child undernutrition, tropical enteropathy, toilets, and handwashing. Lancet. 2009;374:1032–1035. doi: 10.1016/S0140-6736(09)60950-8.
    1. Lai TP, Wright WE, Shay JW. Comparison of Telomere length measurement methods. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 2018;373:20160451. doi: 10.1098/rstb.2016.0451.
    1. Laron Z. In: Hormones, Brain and Behavior. Pfaff DW, Arnold AP, Etgen AM, Fahrbach SE, Rubin RT, editors. Academic Press; 2009. 78 - Growth Hormone and Insulin-Like Growth Factor I: Effects on the brain; pp. 2449–2471.
    1. Lin J, Epel E, Cheon J, Kroenke C, Sinclair E, Bigos M, Wolkowitz O, Mellon S, Blackburn E. Analyses and comparisons of telomerase activity and telomere length in human t and b cells: Insights for epidemiology of telomere maintenance. Journal of Immunological Methods. 2010;352:71–80. doi: 10.1016/j.jim.2009.09.012.
    1. Lin J, Cheon J, Brown R, Coccia M, Puterman E, Aschbacher K, Sinclair E, Epel E, Blackburn EH. Systematic and cell type-specific telomere length changes in subsets of lymphocytes. Journal of Immunology Research. 2016;2016:5371050. doi: 10.1155/2016/5371050.
    1. Lin A, Arnold BF, Mertens AN, Lin J, Benjamin-Chung J, Ali S, Hubbard AE, Stewart CP, Shoab AK, Rahman MZ, Hossen MS, Mutsuddi P, Famida SL, Akther S, Rahman M, Unicomb L, Dhabhar FS, Fernald LCH, Colford JM, Jnr, Luby SP. Effects of water, sanitation, handwashing, and nutritional interventions on telomere length among children in a cluster-randomized controlled trial in rural Bangladesh. eLife. 2017;6:e29365. doi: 10.7554/eLife.29365.
    1. Lin A, Ali S, Arnold BF, Rahman MZ, Alauddin M, Grembi J, Mertens AN, Famida SL, Akther S, Hossen MS, Mutsuddi P, Shoab AK, Hussain Z, Rahman M, Unicomb L, Ashraf S, Naser AM, Parvez SM, Ercumen A, Benjamin-Chung J, Haque R, Ahmed T, Hossain MI, Choudhury N, Jannat K, Alauddin ST, Minchala SG, Cekovic R, Hubbard AE, Stewart CP, Dewey KG, Colford JM, Luby SP. Effects of water, sanitation, handwashing, and nutritional interventions on environmental enteric dysfunction in young children: A cluster-randomized, controlled trial in rural Bangladesh. Clinical Infectious Diseases. 2019;67:1515–1522. doi: 10.1093/cid/ciz291.
    1. Loveridge N, Noble BS. Control of longitudinal growth: The role of nutrition. European Journal of Clinical Nutrition. 1994;48:75–84. doi: 10.1079/pns19930036.
    1. Luby SP, Rahman M, Arnold BF, Unicomb L, Ashraf S, Winch PJ, Stewart CP, Begum F, Hussain F, Benjamin-Chung J, Leontsini E, Naser AM, Parvez SM, Hubbard AE, Lin A, Nizame FA, Jannat K, Ercumen A, Ram PK, Das KK, Abedin J, Clasen TF, Dewey KG, Fernald LC, Null C, Ahmed T, Colford JM. Effects of water quality, sanitation, handwashing, and nutritional interventions on diarrhoea and child growth in rural Bangladesh: A cluster randomised controlled trial. The Lancet Global Health. 2018;6:e302–e315. doi: 10.1016/S2214-109X(17)30490-4.
    1. Masterson EE, Hayes MG, Kuzawa CW, Lee NR, Eisenberg DTA. Early life growth and adult telomere length in a Filipino cohort study. American Journal of Human Biology. 2019;31:e23299. doi: 10.1002/ajhb.23299.
    1. Monaghan P, Ozanne SE. Somatic growth and telomere dynamics in vertebrates: Relationships, mechanisms and consequences. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 2018;373:20160446. doi: 10.1098/rstb.2016.0446.
    1. Nychka D. Bayesian confidence intervals for smoothing splines. Journal of the American Statistical Association. 1988;83:1134–1143. doi: 10.1080/01621459.1988.10478711.
    1. Ong KK, Hardy R, Shah I, Kuh D, National Survey of Health and Development Scientific and Data Collection Teams Childhood stunting and mortality between 36 and 64 years: the British 1946 Birth Cohort Study. The Journal of Clinical Endocrinology and Metabolism. 2013;98:2070–2077. doi: 10.1210/jc.2012-3595.
    1. Price LH, Kao HT, Burgers DE, Carpenter LL, Tyrka AR. Telomeres and early-life stress: An overview. Biological Psychiatry. 2013;73:15–23. doi: 10.1016/j.biopsych.2012.06.025.
    1. Raqib R, Alam DS, Sarker P, Ahmad SM, Ara G, Yunus M, Moore SE, Fuchs G. Low birth weight is associated with altered immune function in rural bangladeshi children: A birth cohort study. The American Journal of Clinical Nutrition. 2007;85:845–852. doi: 10.1093/ajcn/85.3.845.
    1. Ridout SJ, Ridout KK, Kao H-T, Carpenter LL, Philip NS, Tyrka AR, Price LH. Telomeres, early-life stress and mental illness. Advances in Psychosomatic Medicine. 2015;34:92–108. doi: 10.1159/000369088.
    1. Salpea KD, Talmud PJ, Cooper JA, Maubaret CG, Stephens JW, Abelak K, Humphries SE. Association of telomere length with type 2 diabetes, oxidative stress and ucp2 gene variation. Atherosclerosis. 2010;209:42–50. doi: 10.1016/j.atherosclerosis.2009.09.070.
    1. Shalev I, Entringer S, Wadhwa PD, Wolkowitz OM, Puterman E, Lin J, Epel ES. Stress and telomere biology: A lifespan Perspective. Psychoneuroendocrinology. 2013;38:1835–1842. doi: 10.1016/j.psyneuen.2013.03.010.
    1. Takubo K, Izumiyama-Shimomura N, Honma N, Sawabe M, Arai T, Kato M, Oshimura M, Nakamura K-I. Telomere lengths are characteristic in each human individual. Experimental Gerontology. 2002;37:523–531. doi: 10.1016/s0531-5565(01)00218-2.
    1. Verhulst S, Aviv A, Benetos A, Berenson GS, Kark JD. do leukocyte telomere length dynamics depend on baseline telomere length? an analysis that corrects for “regression to the mean.”. European Journal of Epidemiology. 2013;28:859–866. doi: 10.1007/s10654-013-9845-4.
    1. Victora CG, Adair L, Fall C, Hallal PC, Martorell R, Richter L, Sachdev HS, Maternal and Child Undernutrition Study Group Maternal and child undernutrition: Consequences for adult health and human capital. Lancet. 2008;371:340–357. doi: 10.1016/S0140-6736(07)61692-4.
    1. Wadhwa PD, Buss C, Entringer S, Swanson JM. Developmental origins of health and disease: Brief history of the approach and current focus on epigenetic mechanisms. Seminars in Reproductive Medicine. 2009;27:358–368. doi: 10.1055/s-0029-1237424.
    1. Wang H, Naghavi M, Barber RM, Bhutta Z, Carter A, Erskine H. Global, regional, and national life expectancy, all-cause mortality, and cause-specific mortality for 249 causes of death, 1980-2015: A systematic analysis for the global burden of disease study 2015. Lancet. 2016;388:1459–1544. doi: 10.1016/S0140-6736(16)31012-1.
    1. Wood SN, Pya N, Säfken B. Smoothing parameter and model selection for general smooth models. Journal of the American Statistical Association. 2017;111:1548–1563. doi: 10.1080/01621459.2016.1180986.
    1. World Health Organization . Nutrition landscape Information System (NLIS). Country profile indicators. World Health Organization; 2010.
    1. Young AJ. The role of telomeres in the mechanisms and evolution of life-history trade-offs and ageing. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 2018;373:20160452. doi: 10.1098/rstb.2016.0452.
    1. Zole E, Ranka R. Mitochondrial DNA copy number and telomere length in peripheral blood mononuclear cells in comparison with whole blood in three different age groups. Archives of Gerontology and Geriatrics. 2019;83:131–137. doi: 10.1016/j.archger.2019.04.007.

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