Journal Home > Volume 1 , Issue 1
Background

The sex-specific associations between birth weight and the risk of chronic kidney disease (CKD) later in life remain controversial. This study aimed to examine the shape of the relationship between birth weight and the risk of CKD in men and women.

Methods

A total of 277,252 participants free of CKD at baseline from the United Kingdom Biobank (UKB) prospective cohort were included in the analysis. Cox proportional hazard regression model was used to estimate the association between birth weight and the risk of incident CKD with adjustment for potential confounders.

Results

During a median follow-up of 11.9 years, we identified 13,030 (4.7%) CKD cases. Compared with normal birth weight (2.5–4.0 kg), low birth weight (LBW, <2.5 kg) was associated with an 11% higher risk of CKD in men (adjusted hazard ratio [HR]: 1.11 [95% CI 1.01–1.21]) and a 27% higher risk of CKD in women (HR: 1.27 [1.19–1.36]) (p for interaction = 0.02). High birth weight (HBW, >4.0 kg) was associated with an 11% lower risk of CKD (HR: 0.89 [0.83–0.95]) in men but not in women (HR: 0.96 [0.89–1.04]) (p for interaction = 0.13). Furthermore, the LBW-CKD association was stronger in obese (HR: 1.28 [1.18–1.39]) than in nonobese participants (HR: 1.16 [1.09–1.24], p for interaction = 0.03).

Conclusions

We found an L-shaped relationship between birth weight and the risk of CKD in women but a linear shape in men. The LBW-CKD association was mitigated to some extent by maintaining healthy body weight in adulthood. Our findings support the notion that the CKD risk should be managed from a lifecycle perspective.


menu
Abstract
Full text
Outline
About this article

Association between birth weight and the risk of chronic kidney disease in men and women: Findings from a large prospective cohort study

Show Author's information Lingyan Dai1Juncheng Zhuang1,2Li Fan3Xia Zou1Kei Hang Katie Chan4Xueqing Yu1,3 ( )Jie Li1,3,5,6,7 ( )
Global Health Research Center, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, Guangzhou, China
Faculty of Medicine, Macau University of Science and Technology, Macau, China
Department of Nephrology, Guangdong-Hong Kong Joint Laboratory on Immunological and Genetic Kidney Diseases, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China
Departments of Biomedical Sciences and Electrical Engineering, City University of Hong Kong, Hong Kong SAR, China
School of Public Health, Southern Medical University, Guangzhou, China
School of Medicine, South China University of Technology, Guangzhou, China
Department of Epidemiology and Center for Global Cardiometabolic Health, School of Public Health, Brown University, Providence, Rhode Island USA

Abstract

Background

The sex-specific associations between birth weight and the risk of chronic kidney disease (CKD) later in life remain controversial. This study aimed to examine the shape of the relationship between birth weight and the risk of CKD in men and women.

Methods

A total of 277,252 participants free of CKD at baseline from the United Kingdom Biobank (UKB) prospective cohort were included in the analysis. Cox proportional hazard regression model was used to estimate the association between birth weight and the risk of incident CKD with adjustment for potential confounders.

Results

During a median follow-up of 11.9 years, we identified 13,030 (4.7%) CKD cases. Compared with normal birth weight (2.5–4.0 kg), low birth weight (LBW, <2.5 kg) was associated with an 11% higher risk of CKD in men (adjusted hazard ratio [HR]: 1.11 [95% CI 1.01–1.21]) and a 27% higher risk of CKD in women (HR: 1.27 [1.19–1.36]) (p for interaction = 0.02). High birth weight (HBW, >4.0 kg) was associated with an 11% lower risk of CKD (HR: 0.89 [0.83–0.95]) in men but not in women (HR: 0.96 [0.89–1.04]) (p for interaction = 0.13). Furthermore, the LBW-CKD association was stronger in obese (HR: 1.28 [1.18–1.39]) than in nonobese participants (HR: 1.16 [1.09–1.24], p for interaction = 0.03).

Conclusions

We found an L-shaped relationship between birth weight and the risk of CKD in women but a linear shape in men. The LBW-CKD association was mitigated to some extent by maintaining healthy body weight in adulthood. Our findings support the notion that the CKD risk should be managed from a lifecycle perspective.

Keywords: cohort study, birth weight, chronic kidney dieases

References(43)

[1]

Collaboration GBDCKD. Global, regional, and national burden of chronic kidney disease, 1990–2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet. 2020;395(10225):709–33. https://doi.org/10.1016/S0140-6736(20)30045-3

[2]

Michishita R, Matsuda T, Kawakami S, Kiyonaga A, Tanaka H, Morito N, et al. The association between unhealthy lifestyle behaviors and the prevalence of chronic kidney disease (CKD) in middle-aged and older men. J Epidemiol. 2016;26(7):378–85. https://doi.org/10.2188/jea.JE20150202

[3]

Charlton JR, Springsteen CH, Carmody JB. Nephron number and its determinants in early life: a primer. Pediatr Nephrol. 2014;29(12):2299–308. https://doi.org/10.1007/s00467-014-2758-y

[4]

Mitchell EK, Louey S, Cock ML, Harding R, Black MJ. Nephron endowment and filtration surface area in the kidney after growth restriction of fetal sheep. Pediatr Res. 2004;55(5):769–73. https://doi.org/10.1203/01.PDR.0000120681.61201.B4

[5]

Bertram JF, Douglas-Denton RN, Diouf B, Hughson MD, Hoy WE. Human nephron number: implications for health and disease. Pediatr Nephrol. 2011;26(9):1529–33. https://doi.org/10.1007/s00467-011-1843-8

[6]

Li J, Yang Q, An R, Sesso HD, Zhong VW, Chan KHK, et al. Famine and trajectories of body mass index, waist circumference, and blood pressure in two generations: results from the CHNS from 1993–2015. Hypertension. 2022;79(3):518–31. https://doi.org/10.1161/HYPERTENSIONAHA.121.18022

[7]

Li J, Liu S, Li S, Feng R, Na L, Chu X, et al. Prenatal exposure to famine and the development of hyperglycemia and type 2 diabetes in adulthood across consecutive generations: a population-based cohort study of families in Suihua, China. Am J Clin Nutr. 2017;105(1):221–27. https://doi.org/10.3945/ajcn.116.138792

[8]

Li J, Zou X, Zhong F, Yang Q, Manson JE, Papandonatos GD, et al. Prenatal exposure to famine and the development of diabetes later in life: an age-period-cohort analysis of the China health and nutrition survey (CHNS) from 1997 to 2015. Eur J Nutr. 2022;62(2):941–50. https://doi.org/10.1007/s00394-022-03049-w

[9]

Chen C, Nie Z, Wang J, Ou Y, Cai A, Huang Y, et al. Prenatal exposure to the Chinese famine of 1959–62 and risk of cardiovascular diseases in adulthood: findings from the China PEACE million persons project. Eur J Prev Cardiol. 2022;29(16):2111–19. https://doi.org/10.1093/eurjpc/zwac210

[10]

Yu X, Yuan Z, Lu H, Gao Y, Chen H, Shao Z, et al. Relationship between birth weight and chronic kidney disease: evidence from systematics review and two-sample Mendelian randomization analysis. Hum Mol Genet. 2020;29(13):2261–74. https://doi.org/10.1093/hmg/ddaa074

[11]

White SL, Perkovic V, Cass A, Chang CL, Poulter NR, Spector T, et al. Is low birth weight an antecedent of CKD in later life? A systematic review of observational studies. Am J Kidney Dis. 2009;54(2):248–61. https://doi.org/10.1053/j.ajkd.2008.12.042

[12]

Esmeijer K, de Vries AP, Mook-Kanamori DO, de Fijter JW, Rosendaal FR, Rabelink TJ, et al. Low birth weight and kidney function in middle-aged men and women: the Netherlands epidemiology of obesity study. Am J Kidney Dis. 2019;74(6):751–60. https://doi.org/10.1053/j.ajkd.2019.05.007

[13]

Kanzaki G, Tsuboi N, Shimizu A, Yokoo T. Human nephron number, hypertension, and renal pathology. Anat Rec. 2020;303(10):2537–43. https://doi.org/10.1002/ar.24302

[14]

Barry M, Brenner DLG, Anderson S. Glomeruli and blood pressure less of one, more the other? Am J Hypertens. 1988;1(4 Pt 1):335–47. https://doi.org/10.1093/ajh/1.4.335

[15]

Luyckx VA, Perico N, Somaschini M, Manfellotto D, Valensise H, Cetin I, et al. A developmental approach to the prevention of hypertension and kidney disease: a report from the Low Birth Weight and Nephron Number Working Group. Lancet. 2017;390(10092):424–28. https://doi.org/10.1016/S0140-6736(17)30576-7

[16]

Luyckx VA, Brenner BM. Birth weight, malnutrition and kidney-associated outcomes–a global concern. Nat Rev Nephrol. 2015;11(3):135–49. https://doi.org/10.1038/nrneph.2014.251

[17]

Lillas BS, Tondel C, Assmus J, Vikse BE. Low birthweight is associated with lower glomerular filtration rate in middle-aged mainly healthy women. Nephrol Dial Transplant. 2021;37(1):92–9. https://doi.org/10.1093/ndt/gfaa306

[18]

Li S, Chen SC, Shlipak M, Bakris G, McCullough PA, Sowers J, et al. Low birth weight is associated with chronic kidney disease only in men. Kidney Int. 2008;73(5):637–42. https://doi.org/10.1038/sj.ki.5002747

[19]

Hallan S, Euser AM, Irgens LM, Finken MJ, Holmen J, Dekker FW. Effect of intrauterine growth restriction on kidney function at young adult age: the Nord Trondelag Health (HUNT 2) Study. Am J Kidney Dis. 2008;51(1):10–20. https://doi.org/10.1053/j.ajkd.2007.09.013

[20]

Gjerde A, Reisaeter AV, Skrunes R, Marti HP, Vikse BE. Intrauterine growth restriction and risk of diverse forms of kidney disease during the first 50 years of life. Clin J Am Soc Nephrol. 2020;15(10):1413–23. https://doi.org/10.2215/CJN.04080320

[21]

Eriksson JG, Salonen MK, Kajantie E, Osmond C. Prenatal growth and CKD in older adults: longitudinal findings from the Helsinki Birth Cohort Study, 1924–1944. Am J Kidney Dis. 2018;71(1):20–6. https://doi.org/10.1053/j.ajkd.2017.06.030

[22]

Lackland D, Bendall H, Osmond C, Egan BM, Barker DJ. Low birth weights contribute to the high rates of early onset chronic renal failure in the southeastern united states.pdf. JAMA Intern Med. 2000.

[23]

Vikse BE, Irgens LM, Leivestad T, Hallan S, Iversen BM. Low birth weight increases risk for end-stage renal disease. J Am Soc Nephrol. 2008;19(1):151–7. https://doi.org/10.1681/ASN.2007020252

[24]
World Health Organization (WHO) ISCoDaRHP, Tenth Revision, World Health Organization, Geneva, Switzerland, 1992. International statistical classification of diseases and related health problems. Tenth Revision; 1992.
[25]

Inker LA, Schmid CH, Tighiouart H, Eckfeldt JH, Feldman HI, Greene T, et al. Estimating glomerular filtration rate from serum creatinine and cystatin C. N Engl J Med. 2012;367(1):20–9. https://doi.org/10.1056/NEJMoa1114248

[26]

Swartling O, Rydell H, Stendahl M, Segelmark M, Trolle Lagerros Y, Evans M. CKD progression and mortality among men and women: a nationwide study in Sweden. Am J Kidney Dis. 2021;78(2):190–9.e1. https://doi.org/10.1053/j.ajkd.2020.11.026

[27]

Jafar TH, Schmid CH, Stark PC, Toto R, Remuzzi G, Ruggenenti P, et al. The rate of progression of renal disease may not be slower in women compared with men: a patient-level meta-analysis. Nephrol Dial Transplant. 2003;18(10):2047–53. https://doi.org/10.1093/ndt/gfg317

[28]

Al Salmi I, Hoy WE, Kondalsamy-Chennakes S, Wang Z, Healy H, Shaw JE. Birth weight and stages of CKD: a case-control study in an Australian population. Am J Kidney Dis. 2008;52(6):1070–8. https://doi.org/10.1053/j.ajkd.2008.04.028

[29]

Baba M, Shimbo T, Horio M, Ando M, Yasuda Y, Komatsu Y, et al. Longitudinal study of the decline in renal function in healthy subjects. PLoS One. 2015;10(6):e0129036. https://doi.org/10.1371/journal.pone.0129036

[30]

Bikbov B, Perico N, Remuzzi G; on behalf of the GBDGDEG. Disparities in chronic kidney disease prevalence among males and females in 195 countries: analysis of the global burden of disease 2016 study. Nephron. 2018;139(4):313–8. https://doi.org/10.1159/000489897

[31]

Alexander BT, Henry Dasinger J, Intapad S. Effect of low birth weight on women's health. Clin Therapeut. 2014;36(12):1913–23. https://doi.org/10.1016/j.clinthera.2014.06.026

[32]

Hughson M, Farris AB, 3rd, Douglas-Denton R, Hoy WE, Bertram JF. Glomerular number and size in autopsy kidneys: the relationship to birth weight. Kidney Int. 2003;63(6):2113–22. https://doi.org/10.1046/j.1523-1755.2003.00018.x

[33]

Ahmed SB, Ramesh S. Sex hormones in women with kidney disease. Nephrol Dial Transplant. 2016;31(11):1787–95. https://doi.org/10.1093/ndt/gfw084

[34]

Zhao JV, Schooling CM. Sex-specific associations of sex hormone binding globulin with CKD and kidney function: a univariable and multivariable Mendelian randomization study in the UK Biobank. J Am Soc Nephrol. 2021;32(3):686–94. https://doi.org/10.1681/ASN.2020050659

[35]

Oster RT, Luyckx VA, Toth EL. Birth weight predicts both proteinuria and overweight/obesity in a rural population of Aboriginal and non-Aboriginal Canadians. J Dev Orig Health Dis. 2013;4(2):139–45. https://doi.org/10.1017/S2040174412000724

[36]

Luyckx VA, Bertram JF, Brenner BM, Fall C, Hoy WE, Ozanne SE, et al. Effect of fetal and child health on kidney development and long-term risk of hypertension and kidney disease. Lancet. 2013;382(9888):273–83. https://doi.org/10.1016/S0140-6736(13)60311-6

[37]

Hsu CW, Yamamoto KT, Henry RK, De Roos AJ, Flynn JT. Prenatal risk factors for childhood CKD. J Am Soc Nephrol. 2014;25(9):2105–11. https://doi.org/10.1681/ASN.2013060582

[38]

Das SK, Mannan M, Faruque AS, Ahmed T, McIntyre HD, Al Mamun A. Effect of birth weight on adulthood renal function: a bias-adjusted meta-analytic approach. Nephrology. 2016;21(7):547–65. https://doi.org/10.1111/nep.12732

[39]

Wahba IM, Mak RH. Obesity and obesity-initiated metabolic syndrome: mechanistic links to chronic kidney disease. Clin J Am Soc Nephrol. 2007;2(3):550–62. https://doi.org/10.2215/CJN.04071206

[40]

Stasi A, Cosola C, Caggiano G, Cimmarusti MT, Palieri R, Acquaviva PM, et al. Obesity-related chronic kidney disease: principal mechanisms and new approaches in nutritional management. Front Nutr. 2022;9:925619. https://doi.org/10.3389/fnut.2022.925619

[41]

Li J, Liu S. Early life malnutrition is a problem that may be fixed by improving later-life lifestyle: never too late to mend. Heart. 2020;106(3):170–71. https://doi.org/10.1136/heartjnl-2019-316041

[42]

Kramer H. Diet and chronic kidney disease. Adv Nutr. 2019;10(Suppl_4):S367–S79. https://doi.org/10.1093/advances/nmz011

[43]

Xu X, Nie S, Ding H, Hou FF. Environmental pollution and kidney diseases. Nat Rev Nephrol. 2018;14(5):313–24. https://doi.org/10.1038/nrneph.2018.11

Publication history
Copyright
Acknowledgements
Rights and permissions

Publication history

Received: 16 February 2023
Accepted: 25 February 2023
Published: 21 March 2023
Issue date: March 2023

Copyright

© 2023 The Authors. Tsinghua University Press.

Acknowledgements

ACKNOWLEDGMENTS

The authors would like to express their sincere gratitude to all the participants of UK Biobank and all the research assistants involved in building the UK Biobank study. JL was supported by the National Natural Science Foundation of China (81673156, 82073528, and 81302417). XY was supported by Guangdong‐Hong Kong Joint Laboratory on Immunological and Genetic Kidney Diseases (2019B121205005). The funders had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.

Rights and permissions

This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

Return