Calcium urolithiasis course in young stone formers is influenced by the strength of family history: results from a retrospective study
The role of the strength of family history of stones (FHS), i.e., degree of relatives with the disease, on the course of calcium urolithiasis (CU) is not fully understood, particularly in young patients where genetic background has the greatest influence on disease expression. Thus, with a retrospec...
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Published in | Urolithiasis Vol. 45; no. 6; pp. 525 - 533 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.12.2017
Springer Nature B.V |
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Online Access | Get full text |
ISSN | 2194-7228 2194-7236 2194-7236 |
DOI | 10.1007/s00240-016-0955-9 |
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Abstract | The role of the strength of family history of stones (FHS), i.e., degree of relatives with the disease, on the course of calcium urolithiasis (CU) is not fully understood, particularly in young patients where genetic background has the greatest influence on disease expression. Thus, with a retrospective cross-sectional design, we examined baseline clinical parameters and urinary chemistries of 369 subjects (196 M) with CU and 96 controls (41 M) aged between 15 and 25 at the time of the first visit at our stone clinic. Subjects with metabolic syndrome traits, known causes of CU or CU onset before the age of 15 were excluded. Clinical and metabolic parameters were compared among stone formers (SF) and controls, stratified by gender, the presence and type of FHS determined through the kinship coefficient of relatives with stones. No significant differences in clinical course were found between SF with and without FHS, except for the presence of bilateral stones (OR 2.01, 95% CI 1.20–3.39,
p
< 0.01). A significant age-, sex- and disease duration-adjusted trend for a higher number of colics (
p
for trend = 0.001), number of stones (
p
for trend = 0.002), stone rate (
p
for trend = 0.003) and the presence of retained stones (OR 1.60, 95% CI 1.14–2.21,
p
= 0.006) was detected with increasing FHS strength. Urinary chemistries were unaffected by FHS in both SF and controls, except for a higher calcium excretion in females with FHS (
p
< 0.05). The type of FHS, thus, significantly influences the clinical course of CU in young SF, mainly irrespective of urinary factors. |
---|---|
AbstractList | The role of the strength of family history of stones (FHS), i.e., degree of relatives with the disease, on the course of calcium urolithiasis (CU) is not fully understood, particularly in young patients where genetic background has the greatest influence on disease expression. Thus, with a retrospective cross-sectional design, we examined baseline clinical parameters and urinary chemistries of 369 subjects (196 M) with CU and 96 controls (41 M) aged between 15 and 25 at the time of the first visit at our stone clinic. Subjects with metabolic syndrome traits, known causes of CU or CU onset before the age of 15 were excluded. Clinical and metabolic parameters were compared among stone formers (SF) and controls, stratified by gender, the presence and type of FHS determined through the kinship coefficient of relatives with stones. No significant differences in clinical course were found between SF with and without FHS, except for the presence of bilateral stones (OR 2.01, 95% CI 1.20-3.39, p < 0.01). A significant age-, sex- and disease duration-adjusted trend for a higher number of colics (p for trend = 0.001), number of stones (p for trend = 0.002), stone rate (p for trend = 0.003) and the presence of retained stones (OR 1.60, 95% CI 1.14-2.21, p = 0.006) was detected with increasing FHS strength. Urinary chemistries were unaffected by FHS in both SF and controls, except for a higher calcium excretion in females with FHS (p < 0.05). The type of FHS, thus, significantly influences the clinical course of CU in young SF, mainly irrespective of urinary factors. The role of the strength of family history of stones (FHS), i.e., degree of relatives with the disease, on the course of calcium urolithiasis (CU) is not fully understood, particularly in young patients where genetic background has the greatest influence on disease expression. Thus, with a retrospective cross-sectional design, we examined baseline clinical parameters and urinary chemistries of 369 subjects (196 M) with CU and 96 controls (41 M) aged between 15 and 25 at the time of the first visit at our stone clinic. Subjects with metabolic syndrome traits, known causes of CU or CU onset before the age of 15 were excluded. Clinical and metabolic parameters were compared among stone formers (SF) and controls, stratified by gender, the presence and type of FHS determined through the kinship coefficient of relatives with stones. No significant differences in clinical course were found between SF with and without FHS, except for the presence of bilateral stones (OR 2.01, 95% CI 1.20–3.39, p < 0.01). A significant age-, sex- and disease duration-adjusted trend for a higher number of colics (p for trend = 0.001), number of stones (p for trend = 0.002), stone rate (p for trend = 0.003) and the presence of retained stones (OR 1.60, 95% CI 1.14–2.21, p = 0.006) was detected with increasing FHS strength. Urinary chemistries were unaffected by FHS in both SF and controls, except for a higher calcium excretion in females with FHS (p < 0.05). The type of FHS, thus, significantly influences the clinical course of CU in young SF, mainly irrespective of urinary factors. The role of the strength of family history of stones (FHS), i.e., degree of relatives with the disease, on the course of calcium urolithiasis (CU) is not fully understood, particularly in young patients where genetic background has the greatest influence on disease expression. Thus, with a retrospective cross-sectional design, we examined baseline clinical parameters and urinary chemistries of 369 subjects (196 M) with CU and 96 controls (41 M) aged between 15 and 25 at the time of the first visit at our stone clinic. Subjects with metabolic syndrome traits, known causes of CU or CU onset before the age of 15 were excluded. Clinical and metabolic parameters were compared among stone formers (SF) and controls, stratified by gender, the presence and type of FHS determined through the kinship coefficient of relatives with stones. No significant differences in clinical course were found between SF with and without FHS, except for the presence of bilateral stones (OR 2.01, 95% CI 1.20-3.39, p < 0.01). A significant age-, sex- and disease duration-adjusted trend for a higher number of colics (p for trend = 0.001), number of stones (p for trend = 0.002), stone rate (p for trend = 0.003) and the presence of retained stones (OR 1.60, 95% CI 1.14-2.21, p = 0.006) was detected with increasing FHS strength. Urinary chemistries were unaffected by FHS in both SF and controls, except for a higher calcium excretion in females with FHS (p < 0.05). The type of FHS, thus, significantly influences the clinical course of CU in young SF, mainly irrespective of urinary factors.The role of the strength of family history of stones (FHS), i.e., degree of relatives with the disease, on the course of calcium urolithiasis (CU) is not fully understood, particularly in young patients where genetic background has the greatest influence on disease expression. Thus, with a retrospective cross-sectional design, we examined baseline clinical parameters and urinary chemistries of 369 subjects (196 M) with CU and 96 controls (41 M) aged between 15 and 25 at the time of the first visit at our stone clinic. Subjects with metabolic syndrome traits, known causes of CU or CU onset before the age of 15 were excluded. Clinical and metabolic parameters were compared among stone formers (SF) and controls, stratified by gender, the presence and type of FHS determined through the kinship coefficient of relatives with stones. No significant differences in clinical course were found between SF with and without FHS, except for the presence of bilateral stones (OR 2.01, 95% CI 1.20-3.39, p < 0.01). A significant age-, sex- and disease duration-adjusted trend for a higher number of colics (p for trend = 0.001), number of stones (p for trend = 0.002), stone rate (p for trend = 0.003) and the presence of retained stones (OR 1.60, 95% CI 1.14-2.21, p = 0.006) was detected with increasing FHS strength. Urinary chemistries were unaffected by FHS in both SF and controls, except for a higher calcium excretion in females with FHS (p < 0.05). The type of FHS, thus, significantly influences the clinical course of CU in young SF, mainly irrespective of urinary factors. The role of the strength of family history of stones (FHS), i.e., degree of relatives with the disease, on the course of calcium urolithiasis (CU) is not fully understood, particularly in young patients where genetic background has the greatest influence on disease expression. Thus, with a retrospective cross-sectional design, we examined baseline clinical parameters and urinary chemistries of 369 subjects (196 M) with CU and 96 controls (41 M) aged between 15 and 25 at the time of the first visit at our stone clinic. Subjects with metabolic syndrome traits, known causes of CU or CU onset before the age of 15 were excluded. Clinical and metabolic parameters were compared among stone formers (SF) and controls, stratified by gender, the presence and type of FHS determined through the kinship coefficient of relatives with stones. No significant differences in clinical course were found between SF with and without FHS, except for the presence of bilateral stones (OR 2.01, 95% CI 1.20–3.39, p < 0.01). A significant age-, sex- and disease duration-adjusted trend for a higher number of colics ( p for trend = 0.001), number of stones ( p for trend = 0.002), stone rate ( p for trend = 0.003) and the presence of retained stones (OR 1.60, 95% CI 1.14–2.21, p = 0.006) was detected with increasing FHS strength. Urinary chemistries were unaffected by FHS in both SF and controls, except for a higher calcium excretion in females with FHS ( p < 0.05). The type of FHS, thus, significantly influences the clinical course of CU in young SF, mainly irrespective of urinary factors. |
Author | Maggio, Marcello Ticinesi, Andrea Allegri, Franca Pinelli, Silvana Lauretani, Fulvio Guerra, Angela Nouvenne, Antonio Borghi, Loris Meschi, Tiziana Cervellin, Gianfranco |
Author_xml | – sequence: 1 givenname: Angela surname: Guerra fullname: Guerra, Angela organization: Geriatric Rehabilitation Department, University-Hospital of Parma, Department of Clinical and Experimental Medicine, University of Parma – sequence: 2 givenname: Andrea surname: Ticinesi fullname: Ticinesi, Andrea email: andrea.ticinesi@unipr.it organization: Geriatric Rehabilitation Department, University-Hospital of Parma, Department of Clinical and Experimental Medicine, University of Parma – sequence: 3 givenname: Franca surname: Allegri fullname: Allegri, Franca organization: Geriatric Rehabilitation Department, University-Hospital of Parma, Department of Clinical and Experimental Medicine, University of Parma – sequence: 4 givenname: Antonio surname: Nouvenne fullname: Nouvenne, Antonio organization: Geriatric Rehabilitation Department, University-Hospital of Parma, Department of Clinical and Experimental Medicine, University of Parma – sequence: 5 givenname: Silvana surname: Pinelli fullname: Pinelli, Silvana organization: Department of Clinical and Experimental Medicine, University of Parma – sequence: 6 givenname: Fulvio surname: Lauretani fullname: Lauretani, Fulvio organization: Geriatric Rehabilitation Department, University-Hospital of Parma – sequence: 7 givenname: Marcello surname: Maggio fullname: Maggio, Marcello organization: Geriatric Rehabilitation Department, University-Hospital of Parma, Department of Clinical and Experimental Medicine, University of Parma – sequence: 8 givenname: Gianfranco surname: Cervellin fullname: Cervellin, Gianfranco organization: Emergency Department, University-Hospital of Parma – sequence: 9 givenname: Loris surname: Borghi fullname: Borghi, Loris organization: Geriatric Rehabilitation Department, University-Hospital of Parma, Department of Clinical and Experimental Medicine, University of Parma – sequence: 10 givenname: Tiziana surname: Meschi fullname: Meschi, Tiziana organization: Geriatric Rehabilitation Department, University-Hospital of Parma, Department of Clinical and Experimental Medicine, University of Parma |
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CitedBy_id | crossref_primary_10_1007_s00240_019_01156_8 crossref_primary_10_1371_journal_pone_0213180 crossref_primary_10_1016_j_jpurol_2020_03_014 crossref_primary_10_1007_s00240_018_1097_z crossref_primary_10_1089_end_2023_0132 crossref_primary_10_4103_UROS_UROS_20_17 crossref_primary_10_1016_j_urols_2017_07_010 |
Cites_doi | 10.1007/s00240-013-0619-y 10.1053/j.ajkd.2004.06.030 10.1016/S0022-5347(17)42497-9 10.1007/s00240-016-0878-5 10.3109/00365590903151479 10.1210/jc.2013-1834 10.1016/j.urology.2012.06.034 10.1016/j.juro.2008.01.011 10.1001/archinte.1982.00340160084019 10.5527/wjn.v3.i4.256 10.1097/01.ju.0000099789.99127.6b 10.1007/s00240-007-0083-7 10.1681/ASN.2013091011 10.1111/j.1523-1755.2005.00170.x 10.1056/NEJM196806132782403 10.1515/cclm-2013-0618 10.1016/S0022-5347(17)54106-3 10.1007/s40620-015-0225-x 10.1007/s40620-016-0329-y 10.1681/ASN.V74608 10.1681/ASN.V8101568 |
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Keywords | Disease activity Nephrolithiasis Recurrent Kinship coefficient Familiality Idiopathic calcium stones |
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SubjectTerms | Adolescent Adult Age Factors Calcium - metabolism Calcium - urine Cross-Sectional Studies Family medical history Female Humans Kidney Calculi - epidemiology Kidney Calculi - etiology Kidney Calculi - urine Male Medical Biochemistry Medical History Taking - statistics & numerical data Medicine Medicine & Public Health Metabolism Nephrology Original Paper Recurrence Renal Elimination Retrospective Studies Risk Factors Sex Factors Urology Young Adult |
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Title | Calcium urolithiasis course in young stone formers is influenced by the strength of family history: results from a retrospective study |
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