#METABOLOMICS WORKBENCH michaelsa93_20170509_153519 DATATRACK_ID:902 STUDY_ID:ST000603 ANALYSIS_ID:AN000923 PROJECT_ID:PR000440
VERSION             	1
CREATED_ON             	May 10, 2017, 1:52 pm
#PROJECT
PR:PROJECT_TITLE                 	Urinary Volatile Compound, Associated with Chronic Inflammation In Interstitial
PR:PROJECT_TITLE                 	Cystitis
PR:PROJECT_SUMMARY               	Interstitial cystitis (IC)/bladder pain syndrome (BPS) is a clinical condition
PR:PROJECT_SUMMARY               	that manifests as a sensory hypersensitivity of unknown cause and is
PR:PROJECT_SUMMARY               	characterized by urinary frequency, bladder discomfort, and pelvic pain. In the
PR:PROJECT_SUMMARY               	present volatolomic study, we have analyzed the VOCs unique to urine specimens
PR:PROJECT_SUMMARY               	obtained from interstitial cystitis patients, in compassion to healthy
PR:PROJECT_SUMMARY               	controls.This is the novel finding from comprehensive and unbiased metabolomics
PR:PROJECT_SUMMARY               	analysis that urinary menthol is decreased in urine specimens from IC patients,
PR:PROJECT_SUMMARY               	and that the reduced menthol level in IC is potentially linked to the chronic
PR:PROJECT_SUMMARY               	inflammation, which is often observed in IC patients
PR:INSTITUTE                     	Cedars-Sinai Medical Center
PR:LAST_NAME                     	Kim
PR:FIRST_NAME                    	Jayoung
PR:ADDRESS                       	8700 Beverly Blvd. Davis Research Building Ste 5071 Los Angeles, CA 90048
PR:EMAIL                         	jayoung.kim@cshs.org
PR:PHONE                         	310-423-7168
#STUDY
ST:STUDY_TITLE                   	Urinary Volatile Compound, Associated with Chronic Inflammation In Interstitial
ST:STUDY_TITLE                   	Cystitis
ST:STUDY_SUMMARY                 	Interstitial cystitis (IC)/bladder pain syndrome (BPS) is a clinical condition
ST:STUDY_SUMMARY                 	that manifests as a sensory hypersensitivity of unknown cause and is
ST:STUDY_SUMMARY                 	characterized by urinary frequency, bladder discomfort, and pelvic pain. In the
ST:STUDY_SUMMARY                 	present volatolomic study, we have analyzed the VOCs unique to urine specimens
ST:STUDY_SUMMARY                 	obtained from interstitial cystitis patients, in compassion to healthy
ST:STUDY_SUMMARY                 	controls.This is the novel finding from comprehensive and unbiased metabolomics
ST:STUDY_SUMMARY                 	analysis that urinary menthol is decreased in urine specimens from IC patients,
ST:STUDY_SUMMARY                 	and that the reduced menthol level in IC is potentially linked to the chronic
ST:STUDY_SUMMARY                 	inflammation, which is often observed in IC patients
ST:INSTITUTE                     	University of California, Davis
ST:DEPARTMENT                    	Genome and Biomedical Sciences Facility
ST:LABORATORY                    	WCMC Metabolomics Core
ST:LAST_NAME                     	Fiehn
ST:FIRST_NAME                    	Oliver
ST:ADDRESS                       	Health Sciences Drive, Davis, California, 95616, USA
ST:EMAIL                         	ofiehn@ucdavis.edu
ST:PHONE                         	(530) 754-8258
#SUBJECT
SU:SUBJECT_TYPE                  	Human
SU:SUBJECT_SPECIES               	Homo sapiens
SU:TAXONOMY_ID                   	9606
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Additional sample data
SUBJECT_SAMPLE_FACTORS           	C10_001	160427blvsa17_1	Treatment:control	Source=Urine
SUBJECT_SAMPLE_FACTORS           	C13_002	160427blvsa10_1	Treatment:control	Source=Urine
SUBJECT_SAMPLE_FACTORS           	C15_003	160427blvsa09_1	Treatment:control	Source=Urine
SUBJECT_SAMPLE_FACTORS           	C16_004	160427blvsa08_1	Treatment:control	Source=Urine
SUBJECT_SAMPLE_FACTORS           	C17_005	160427blvsa19_1	Treatment:control	Source=Urine
SUBJECT_SAMPLE_FACTORS           	C18_006	160427blvsa15_1	Treatment:control	Source=Urine
SUBJECT_SAMPLE_FACTORS           	C26_007	160427blvsa14_1	Treatment:control	Source=Urine
SUBJECT_SAMPLE_FACTORS           	C27_008	160427blvsa05_1	Treatment:control	Source=Urine
SUBJECT_SAMPLE_FACTORS           	C28_009	160427blvsa18_1	Treatment:control	Source=Urine
SUBJECT_SAMPLE_FACTORS           	C33_010	160427blvsa13_1	Treatment:control	Source=Urine
SUBJECT_SAMPLE_FACTORS           	IC12_013	160427blvsa01_1	Treatment:IC	Source=Urine
SUBJECT_SAMPLE_FACTORS           	IC14_014	160427blvsa20_1	Treatment:IC	Source=Urine
SUBJECT_SAMPLE_FACTORS           	IC19_015	160427blvsa12_1	Treatment:IC	Source=Urine
SUBJECT_SAMPLE_FACTORS           	IC20_016	160427blvsa02_1	Treatment:IC	Source=Urine
SUBJECT_SAMPLE_FACTORS           	IC22_017	160427blvsa04_1	Treatment:IC	Source=Urine
SUBJECT_SAMPLE_FACTORS           	IC30_018	160427blvsa11_1	Treatment:IC	Source=Urine
SUBJECT_SAMPLE_FACTORS           	IC31_019	160427blvsa07_1	Treatment:IC	Source=Urine
SUBJECT_SAMPLE_FACTORS           	IC43_020	160427blvsa03_1	Treatment:IC	Source=Urine
SUBJECT_SAMPLE_FACTORS           	IC5_011	160427blvsa16_1	Treatment:IC	Source=Urine
SUBJECT_SAMPLE_FACTORS           	IC9_012	160427blvsa06_1	Treatment:IC	Source=Urine
#COLLECTION
CO:COLLECTION_SUMMARY            	First morning urine specimens were obtained using clean catch methods, and sent
CO:COLLECTION_SUMMARY            	to clinical laboratory. After a 10 min centrifugation to remove cell debris,
CO:COLLECTION_SUMMARY            	urine specimens were stored at −80◦C until further analysis.
#TREATMENT
TR:TREATMENT_SUMMARY             	No treatment
#SAMPLEPREP
SP:SAMPLEPREP_SUMMARY            	1. Vortex the urine samples for about 10s to obtain a homogenized sample using
SP:SAMPLEPREP_SUMMARY            	the MiniVortexer VWR. 2. Aliquot 15-30ul and add 1ml extraction solution. The
SP:SAMPLEPREP_SUMMARY            	extraction solution has to be pre-chilled using the ThermoElectron Neslab RTE
SP:SAMPLEPREP_SUMMARY            	740 cooling bath set to -20°C. 3. Vortex the sample for about 10s and shake for
SP:SAMPLEPREP_SUMMARY            	5min at 4°C using the Orbital Mixing Chilling/Heating plate. If you are using
SP:SAMPLEPREP_SUMMARY            	more than one sample, keep the rest of the samples on ice (chilled at <0°C with
SP:SAMPLEPREP_SUMMARY            	NaCl). 4. Centrifuge samples for 2min at 14000 rcf using the centrifuge
SP:SAMPLEPREP_SUMMARY            	Eppendorf 5415 D. 5. Aliquot 2X 0.5ml supernatant. One for analysis and one for
SP:SAMPLEPREP_SUMMARY            	backup. Store 2nd aliquot in -20°C freezer. 6. Evaporate 0.5ml aliquots of the
SP:SAMPLEPREP_SUMMARY            	sample in the Labconco Centrivap cold trap concentrator to complete dryness. 7.
SP:SAMPLEPREP_SUMMARY            	Submit to derivatization.
SP:SAMPLEPREP_PROTOCOL_FILENAME  	SOP_Extraction_of_Urine.pdf
#CHROMATOGRAPHY
CH:CHROMATOGRAPHY_TYPE           	GC
CH:INSTRUMENT_NAME               	Agilent
CH:COLUMN_NAME                   	Restek Rtx-5Sil MS (30 x 0.25mm, 0.25um)
CH:COLUMN_NAME                   	0.25 μm film made of 95% dimethyl/5%diphenylpolysiloxane)
CH:FLOW_RATE                     	1 ml/min
CH:COLUMN_TEMPERATURE            	50 - 330°C
CH:COLUMN_PRESSURE               	7.7 PSI (initial condition)
CH:INJECTION_TEMPERATURE         	50°C ramped to 250°C by 12°C/s
CH:SAMPLE_INJECTION              	0.5µl
CH:OVEN_TEMPERATURE              	50°C for 1 min, then ramped at 20°C/min to 330°C, held constant for 5 min
CH:TRANSFERLINE_TEMPERATURE      	230°C
CH:WASHING_BUFFER                	Ethyl Acetate
CH:SAMPLE_LOOP_SIZE              	30 m length x 0.25 mm internal diameter
CH:RANDOMIZATION_ORDER           	Excel generated
#ANALYSIS
AN:ANALYSIS_TYPE                 	MS
#MS
MS:MS_COMMENTS                   	-
MS:INSTRUMENT_NAME               	Varian 210-MS GC Ion Trap
MS:INSTRUMENT_TYPE               	GC Ion Trap
MS:MS_TYPE                       	EI
MS:ION_MODE                      	POSITIVE
MS:ION_SOURCE_TEMPERATURE        	250°C
MS:IONIZATION_ENERGY             	70eV
MS:MASS_ACCURACY                 	Nominal
MS:SOURCE_TEMPERATURE            	250°C
MS:SCANNING_CYCLE                	17 Hz
MS:SCANNING_RANGE                	85-500
MS:SKIMMER_VOLTAGE               	1850 V
#MS_METABOLITE_DATA
MS_METABOLITE_DATA:UNITS         	Counts
MS_METABOLITE_DATA_START
Samples	160427blvsa17_1	160427blvsa10_1	160427blvsa09_1	160427blvsa08_1	160427blvsa19_1	160427blvsa15_1	160427blvsa14_1	160427blvsa05_1	160427blvsa18_1	160427blvsa13_1	160427blvsa01_1	160427blvsa20_1	160427blvsa12_1	160427blvsa02_1	160427blvsa04_1	160427blvsa11_1	160427blvsa07_1	160427blvsa03_1	160427blvsa16_1	160427blvsa06_1
Factors	Treatment:control	Treatment:control	Treatment:control	Treatment:control	Treatment:control	Treatment:control	Treatment:control	Treatment:control	Treatment:control	Treatment:control	Treatment:IC	Treatment:IC	Treatment:IC	Treatment:IC	Treatment:IC	Treatment:IC	Treatment:IC	Treatment:IC	Treatment:IC	Treatment:IC
2-Heptanone, 4,6-dimethyl-	10861	7432	5502	6840	5128	4226	2158	7012	1970	4502	1878	8494	8236	5210	2339	2734	7868	8040	6328	9536
2-Heptanone, 4-methyl-	21740	16862	10920	13605	9814	7831	3308	16918	3006	8439	4078	21001	19064	9155	6732	1920	19844	15833	14307	21256
2-Heptanone	2499	3935	2817	2610	2188	7432	5034	4263	3753	4614	2139	2873	1668	1254	5474	1772	2325	2153	9130	4145
4-Heptanone	22915	97506	25148	55730	76229	194896	227266	75812	109550	30610	270328	32209	64385	24148	97657	43861	21656	108689	51015	28037
Benzaldehyde, 4-methyl-	7241	4509	6192	12714	3429	5000	1937	4685	3044	8964	1538	4321	3985	6255	1567	1461	4092	3869	3941	5290
Benzaldehyde	2708	980	775	13614	989	1204	4955	72550	395	1315	678	1287	4258	860	2094	752	2208	1724	2387	9863
Benzene, 1,3-bis(1,1-dimethylethyl)-	5752	6890	4977	11361	5647	4020	2890	6351	2165	5613	2039	7510	4888	5988	1775	934	54663	6986	5604	6729
Benzoic acid, 2-[(trimethylsilyl)oxy]-, trimethylsilyl ester	1728	903	540	905	2353	612	543	1401	446	1354	363	1938	780	728	877	242	1206	1987	2509	2173
Ethylbenzene	5469	7338	7928	9139	9591	1951	3913	8232	2683	5854	2694	37113	4031	2464	1995	1008	19764	7003	6735	7095
Hexaethylene glycol dimethyl ether	3959	2718	1462	2390	3287	1696	1424	2035	745	3435	758	3763	2267	2011	1173	556	3147	4114	3049	3498
o-Xylene	5469	7338	7928	9139	9591	1951	3913	8232	2683	5854	2694	37113	4031	2464	1995	1008	19764	7003	6735	7095
styrene	5694	5952	6046	9125	5211	3857	2148	3883	1701	11155	2482	7158	5587	2720	2525	2762	12263	7661	5683	8493
t-Butyl ethyl ether2	19150	16797	21771	31084	14606	6027		12141	4844	15827	2718	12724	17674	10631	3646	1921	7068	6335	10015	13762
Thiocyanic acid, 2-propenyl ester		1497	7474	833	2829	2916	3464	1262	1644	500	3641	604	938	853	2502	1118	438	1501	2719	3525
toluene	14670	9597	8101	16070	10241	4590		8416	2275	11930	2625	11644	7317	10860	5870	2138	21443	13956	8567	15523
2-Pentanone	22291	54326	9230	26189		26576	27101	10988	148235	109629	8343	41454	27360	9284	20193	15496	14910		27096	18913
2-Propanol, 2-methyl-	10570	11793	14042	21161		4829	2757		4943	16289	2002	8254	15429	9159	2863	3264	7357		7740	8137
Allyl Isothiocyanate		2904	96579	922	38086	2874	12804	14705	1222		41249	1665		6807	29864	13503	1342	1864	35167	42954
Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1à,2á,5à)-(ñ)-	631	4233	2410	3701	550	3309	3008	1374	1344	751	487	1934	465	363	1980	672	734	3069		664
Hexane	29240	22285	13531	21648	29652	11431	11420	18595	5738	24555	6243	28767	18169	15314	9401	4209	27628		27939	35528
Phenol, 2,4-bis(1,1-dimethylethyl)-	114302	27501	79083	46418	4244	2351	2159	56210	9444	2498	5471	60716	2884	4095	1807	339		4151	44321	65989
Phenol					2159	12587	971	2087		2356	805		1813	1873	1105	1145	2692	3469	2494	3406
Propylamine	10570	11793	14042	21161		4829	2757		4943	16289	2002	8254	15429	9159	2863	3264	7357		7740	8137
Pyrrole	3077	21755	1389	8889	3546	3295	3162		1552		2576	10147	7493	5972	1431	2415		9118	2841	2998
4-pentenal, 2-methyl	7250	4696	3604	5428	5415		2484	4267	1593		1636	7198			2654	982	7371	23720	5493	8481
Benzaldehyde, 3,5-dimethyl-			572	2478	115570	32812	35564	4001	149	3156		2861	108044	217998	60008		90361	115872	2285	2102
Benzene, (1-methylethyl)-	4359	3214	1958	3525	3574	1754	1565	3959	716	3876	1049	4502	2466	2248			4844	5711	3826	5167
Acetophenone	3181	1604	1033			912			444	1956	411	1869	1808	984	652	12370			422	
Methyl Isobutyl Ketone	5892	7377	4104	5570	4285	3209	3157	4942	907	8840	1853	7068	5401		2098	2868	5013			6861
1-Hexanol, 2-ethyl-	4607	2308	1913	1535		1013	1036	4082		11321			3103	1615	832	124913		2668	2351	
2-Cyclohexen-1-one, 2-methyl-5-(1-methylethenyl)-, (S)-	12738		1219	3192		14404	2097	8130	7067		2488		3659		44750	504		8866	51148	
Benzene, (1-methyl-1-butenyl)-	1778	3005	565	1852		1609	2147		1686	1383		1318	865		504	829	1788		1445	
Benzene, (2-isothiocyanatoethyl)-	16012	6029	5278	1786		533		1920	782		1782			783	1055	2461			7684	18438
benzoylformic acid			500	652				676		1143			1129	1537	358	374	1258			1614
Benzene, chloro-			1091	2290	3426	1229	1716	5848	549				1476	3395	907	485	4727			
Cyclohexanone						539					232	2010			3530	39025			1142	
Cyclopropane, isothiocyanato-			2420		1914						974				792	392			1166	1921
2-Cyclohexen-1-one, 3-methyl-6-(1-methylethyl)-		1193	1560		1715			2792	570						50578	4395		1391	7039	
2-Propenoic acid, 2-methyl-, 1,2-ethanediyl ester													1968			16093	2005			
4-Carene, (1S,3R,6R)-(-)-		604				728	1330						2726				874	1361		
Amylene Hydrate			1713		1119								1956			337	1185			
Benzaldehyde, 2,5-dimethyl-														1917	549			1121		
1-Octanol															414	714				
2,4,6-Octatrienal							737						2246		385					
2-Cyclohexen-1-one, 3,5,5-trimethyl-													1584			54906				
5-Methyl-1-heptanol						352		242							180	911				
Propofol					897				46898	52658						9366				
MS_METABOLITE_DATA_END
#METABOLITES
METABOLITES_START
metabolite_name	m/z
2-Heptanone, 4,6-dimethyl-	423.714
2-Heptanone, 4-methyl-	396.607
2-Heptanone	370.794
4-Heptanone	360.151
Benzaldehyde, 4-methyl-	478.457
Benzaldehyde	414.835
Benzene, 1,3-bis(1,1-dimethylethyl)-	550.546
Benzoic acid, 2-[(trimethylsilyl)oxy]-, trimethylsilyl ester	588.472
Ethylbenzene	361.151
Hexaethylene glycol dimethyl ether	648.859
o-Xylene	361.092
styrene	373.146
t-Butyl ethyl ether2	228.028
Thiocyanic acid, 2-propenyl ester	362.033
toluene	301.939
2-Pentanone	259.78
2-Propanol, 2-methyl-	201.097
Allyl Isothiocyanate	366.56
Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1à,2á,5à)-(ñ)-	520.734
Hexane	316.933
Phenol, 2,4-bis(1,1-dimethylethyl)-	652.799
Phenol	417.658
Propylamine	200.803
Pyrrole	292.414
4-pentenal, 2-methyl	321.108
Benzaldehyde, 3,5-dimethyl-	540.902
Benzene, (1-methylethyl)-	429.182
Acetophenone	469.284
Methyl Isobutyl Ketone	287.239
1-Hexanol, 2-ethyl-	443.353
2-Cyclohexen-1-one, 2-methyl-5-(1-methylethenyl)-, (S)-	551.78
Benzene, (1-methyl-1-butenyl)-	527.026
Benzene, (2-isothiocyanatoethyl)-	643.92
benzoylformic acid	481.75
Benzene, chloro-	348.215
Cyclohexanone	378.497
Cyclopropane, isothiocyanato-	357.329
2-Cyclohexen-1-one, 3-methyl-6-(1-methylethyl)-	557.19
2-Propenoic acid, 2-methyl-, 1,2-ethanediyl ester	573.713
4-Carene, (1S,3R,6R)-(-)-	461.522
Amylene Hydrate	240.258
Benzaldehyde, 2,5-dimethyl-	536.375
1-Octanol	465.168
2,4,6-Octatrienal	421.715
2-Cyclohexen-1-one, 3,5,5-trimethyl-	496.214
5-Methyl-1-heptanol	451.232
Propofol	596.174
METABOLITES_END
#END